Category Archives: Epigenetics

Epigenetics is a stream of genetics that involves the study of variations in cellular and physiological characteristics initiated by external or ecological aspects, which turn genes on and off and affect the cellular ability to read genes unaffected by the changes. of the genotype. Epigenetics results in changes in the phenotype of an organism rather than in the genotype, where the underlying DNA or RNA sequence remains unchanged. Epigenetic alterations are essential for development because they are dynamic and change according to environmental stimuli.

Epigenetics-Based Kits Market research is an intelligence report with meticulous efforts undertaken to study the right and valuable information. The data which has been looked upon is done considering both, the existing top players and the upcoming competitors. Business strategies of the key players and the new entering market industries are studied in detail. Well explained SWOT analysis, revenue share and contact information are shared in this report analysis.

Epigenetics-Based Kits Market is growing at a 13.61% CAGR during the forecast period 2020-2026. The increasing interest of the individuals in this industry is that the major reason for the expansion of this market.

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Top Companies of this Market includes: Active Motif, Promega Corporation, Thermo Fisher Scientific , New England Biolabs, Agilent Technologies, PerkinElmer Inc, Bio-Rad Laboratories, Shivom Ventures Limited, AsisChem Inc, Enzo Life Sciences, EpiGentek Group Inc, BioVision Inc, GeneTex.

The global Epigenetics-Based Kits market is analyzed in terms of its competitive landscape. For this, the report encapsulates data on each of the key players in the market according to their current company profile, gross margins, sale price, sales revenue, sales volume, product specifications along with pictures, and the latest contact information. The reports conclusion leads into the overall scope of the global market with respect to feasibility of investments in various segments of the market, along with a descriptive passage that outlines the feasibility of new projects that might succeed in the global Epigenetics-Based Kits market in the near future.

The report provides insights on the following pointers:

Market Penetration: Comprehensive information on the product portfolios of the top players in the Epigenetics-Based Kits market.

Product Development/Innovation: Detailed insights on the upcoming technologies, R&D activities, and product launches in the market.

Competitive Assessment: In-depth assessment of the market strategies, geographic and business segments of the leading players in the market.

Market Development: Comprehensive information about emerging markets. This report analyzes the market for various segments across geographies.

Market Diversification: Exhaustive information about new products, untapped geographies, recent developments, and investments in the Epigenetics-Based Kits market.

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The cost analysis of the Global Epigenetics-Based Kits Market has been performed while keeping in view manufacturing expenses, labor cost, and raw materials and their market concentration rate, suppliers, and price trend. Other factors such as Supply chain, downstream buyers, and sourcing strategy have been assessed to provide a complete and in-depth view of the market. Buyers of the report will also be exposed to a study on market positioning with factors such as target client, brand strategy, and price strategy taken into consideration.

Key Influence of the Epigenetics-Based Kits Market report:

Table of Contents

Global Epigenetics-Based Kits Market Research Report 2020

Chapter 1 Epigenetics-Based Kits Market Overview

Chapter 2 Global Economic Impact on Industry

Chapter 3 Global Market Competition by Manufacturers

Chapter 4 Global Production, Revenue (Value) by Region

Chapter 5 Global Supply (Production), Consumption, Export, Import by Regions

Chapter 6 Global Production, Revenue (Value), Price Trend by Type

Chapter 7 Global Market Analysis by Application

Chapter 8 Manufacturing Cost Analysis

Chapter 9 Industrial Chain, Sourcing Strategy and Downstream Buyers

Chapter 10 Marketing Strategy Analysis, Distributors/Traders

Chapter 11 Market Effect Factors Analysis

Chapter 12 Global Epigenetics-Based Kits Market Forecast

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Epigenetics-Based Kits Market Recovery and Impact Analysis Report Active Motif, Promega Corporation, Thermo Fisher Scientific , New England Biolabs,...

AUSTIN, Texas, June 21, 2021 (GLOBE NEWSWIRE) -- VolitionRx Limited ( AMERICAN: VNRX) ("Volition"), a multi-national epigenetics company developing simple, easy to use, cost effective blood tests to help diagnose a range of cancers and other diseases in both humans and animals, today announced that Scott Powell, EVP of Investor Relations and Chief Financial Officer of Volition America Inc., will present live at LifeSciencesInvestorForum.com on June 24th.

DATE: Thursday, June 24th TIME: 1:30 PM ETLINK: https://bit.ly/3c7Ertp

This will be a live, interactive online event where investors are invited to ask the company questions in real-time. If attendees are not able to join the event live on the day of the conference, an archived webcast will also be made available after the event.

It is recommended that investors pre-register and run the online system check to expedite participation and receive event updates.

Learn more about the event at http://www.lifesciencesinvestorforum.com.

About VolitionRx Limited

Volition is a multi-national epigenetics company developing simple, easy to use, cost effective blood tests to help diagnose a range of cancers and other diseases. Early diagnosis has the potential to not only prolong the life of patients, but also to improve their quality of life. The tests are based on the science of Nucleosomics, which is the practice of identifying and measuring nucleosomes in the bloodstream or other bodily fluid - an indication that disease is present. Volition is primarily focused on human diagnostics but also has a subsidiary focused on animal diagnostics.

Volition's research and development activities are centered in Belgium, with a small laboratory in California and additional offices in Texas, London and Singapore, as the company focuses on bringing its diagnostic products to market.

For more information about Volition, visit Volition's website volition.com or connect with us via: Twitter: https://twitter.com/volitionrx LinkedIn: https://www.linkedin.com/company/volitionrx Facebook: https://www.facebook.com/VolitionRx/

The contents found at Volition's website address, Twitter, LinkedIn, Facebook, and YouTube are not incorporated by reference into this document and should not be considered part of this document. The addresses for Volition's website, Twitter, LinkedIn, Facebook, and YouTube are included in this document as inactive textual references only.

About Life Sciences Investor Forum

Life Sciences Investor Forum is the leading proprietary investor conference series that provides an interactive forum for Life Sciences companies to meet with and present directly to investors.

A real-time solution for investor engagement, Life Sciences Investor Forum is powered by Intrado Digital Media and specifically designed for more efficient investor access. Replicating the look and feel of on-site investor conferences, Life Sciences Investor Forum combines leading-edge conferencing and investor communications capabilities with a comprehensive global investor audience network.

See the article here:
VolitionRx Limited to Webcast Live at Life Sciences Investor Forum June 24th - GuruFocus.com

Enhancing liquid biopsies

Liquid biopsies, analyses of cell-free DNA that circulates in the blood, can be used in prenatal testing, oncology, and to monitor organ transplant recipients. Lo et al. review the nongenetic information that can be gleaned from analyses of cell-free DNA, which offers additional promise for the applications of this procedure. These analyses include DNA methylation patterns, fragmentation profiles, and topology, which can be informative about the health and origin of the tissue from which they are derived.

Science, this issue p. eaaw3616

Liquid biopsies that are based on analysis of cell-free DNA from plasma offer diagnostic information that is otherwise accessible conventionally through invasive biopsies. Noninvasive prenatal testing has been used globally for the screening of fetal chromosomal aneuploidies and has led to a considerable reduction in invasive prenatal testing, such as use of amniocentesis. Cancer liquid biopsies have been used for the selection of targeted therapies and monitoring of disease progression. Liquid biopsies for organ transplant patients have been used to monitor graft dysfunction. The first applications of liquid biopsies are based on the detection of genetic markers in cell-free DNA, such as sex differences, genetic polymorphisms, or mutations. By studying nongenetic features of cell-free DNA moleculesincluding DNA methylation, fragmentation, and topologyunderstanding of cell-free DNA biology has expanded the spectrum and utilities of liquid biopsies.

Cell-free DNA in plasma consists of a mixture of fragmented DNA molecules released from various tissues within the body. Each cell-free DNA fragment bears molecular signatures of its cell of origin, such as DNA methylation status. The methylation profile of circulating fetal DNA in the mothers plasma correlates with that of the placenta and has been exploited as a means to develop noninvasive fetus-specific biomarkers that are not dependent on fetal sex or genotype. Circulating tumor-derived DNA bear methylation states that resemble the tumor tissue and have enabled the development of tests for the screening and localization of cancer. The fragmentation of plasma DNA is related to the nucleosomal organization, chromatin structure, gene expression, and nuclease content of the tissue of origin, resulting in characteristic signatures in the form of fragment size, nucleotide motifs at the fragment ends, single-stranded jagged ends, and the genomic locations of the fragmentation endpoints. For mitochondrial DNA that is originally in a circular form, fragmentation will also change its topology into a linear form. By noting these features of cell-free DNA fragments, the anatomical site of pathology could potentially be deduced, providing additional information than just quantifying mitochondrial DNA without regard to its form. The study of such characteristics has also enhanced our understanding of the biology and generation of cell-free DNA. The roles of nucleases in plasma DNA biology, such as deoxyribonuclease 1like-3, have been explored by using gene-deletion mouse models and confirmed in humans bearing nuclease gene mutations, with potential implications for the pathogenesis of autoimmune diseases.

The use of DNA methylation, fragmentomic, and topologic analyses of circulating DNA, either in a targeted fashion or in a genomewide manner, will be expected to impact clinical practice. Clinical specimens covering more disease entities will need to be investigated to identify tissue-specific and disease-relevant signatures. During the discovery phase, to better delineate these signatures, mining is performed on high volumes of DNA data pooled within and across samples by using customized bioinformatics algorithms. Once these putative sets of signatures have been identified, signature- and target-specific assays could be developed, and large-scale clinical trials will be needed to validate these approaches. One application is in the development of plasma DNAbased cancer screening. One advantage of these approaches is the potentially large number of markers that can be developed to differentiate cancer and noncancer cells and in the ability to locate the tissue of origin of the detected cancer, possibly including cancers of unknown primary. In the area of noninvasive prenatal testing, the correlation of DNA methylation, fragmentomic, and topologic aberrations in circulating DNA to clinical outcomes would expand the spectrum of diagnostic applications beyond current ones. Fragmentomic approaches have the potential for enriching the cell-free DNA species of interest, such as through the use of automated platforms that allow the size separation of circulating DNA. In the area of organ transplant monitoring, the development of DNA methylation, fragmentomic, and topologic markers would provide an alternative to genetic markers for detecting rejection. These nongenetic markers may enable further differentiation of the donors contribution to the circulating DNA pool into its constituent tissue components. The understanding between circulating DNA and nucleases is in its infancy. Circulating DNA signatures attributable to changes in nuclease expression in health and disease need to be elucidated and may have emerging diagnostic applications.

Different tissues, including cancer cells and trophoblasts in pregnancy, contribute cell-free DNA to the circulation. The cell-free DNA molecules may bear methylation states reflective of the cell of origin. The DNA molecule size, fragment end locations, and end motifs are influenced by the nucleosome organization, chromatin structure, nuclease content, and gene expression of the tissue of origin. Parameters that can be measured to quantify these characteristics are shown on the right.

Liquid biopsies that analyze cell-free DNA in blood plasma are used for noninvasive prenatal testing, oncology, and monitoring of organ transplant recipients. DNA molecules are released into the plasma from various bodily tissues. Physical and molecular features of cell-free DNA fragments and their distribution over the genome bear information about their tissues of origin. Moreover, patterns of DNA methylation of these molecules reflect those of their tissue sources. The nucleosomal organization and nuclease content of the tissue of origin affect the fragmentation profile of plasma DNA molecules, such as fragment size and end motifs. Besides double-stranded linear fragments, other topological forms of cell-free DNA also existnamely circular and single-stranded molecules. Enhanced by these features, liquid biopsies hold promise for the noninvasive detection of tissue-specific pathologies with a range of clinical applications.

Continue reading here:
Epigenetics, fragmentomics, and topology of cell-free DNA in liquid biopsies - Science

Epigenetics-based instruments marketis expected to register a substantial CAGR in the forecast period of 2019-2026. The report contains data from the base year of 2018 and the historic year of 2017. This rise in market value can be attributed to the various innovations and advancements of technologies associated with epigenetics.

The persuasive Epigenetics-Based Instruments market report displays a comprehensive study on production capacity, consumption, import and export for all the major regions across the globe. Analysis and discussion of important industry trends, market size, and market share are estimated in the report. The report uses an excellent research methodology which focuses on market share analysis and key trend analysis. The market research report plays a key role in developing the strategies for sales, advertising, marketing, and promotion. Key insights of the Epigenetics-Based Instruments advertising report are complete and distinct analysis of the market drivers and restraints, major market players involved in this industry, detailed analysis of the market segmentation and competitive analysis of the key players involved.

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Few of the major competitors currently working in the global epigenetics-based instruments market arePacific Biosciences of California, Inc.; 10x Genomics; Illumina, Inc.; Merck KGaA; QIAGEN; Eisai Co., Ltd.; Novartis AG; Diagenode s.a.; Zymo Research; Active Motif, Inc.; Thermo Fisher Scientific Inc.; Agilent Technologies, Inc.; Bio-Rad Laboratories, Inc.; Bio-Techne among others.

Key Developments in the Market:

Market Drivers

Market Restraints

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Segmentation: Global Epigenetics-Based Instruments Market

By Product

By Technology

By Application

By End-Users

ByGeography

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Global Epigenetics-Based Instruments Market to Deliver Prominent Growth & Striking Opportunities, Analysis By Active Motif, Inc.; Thermo Fisher...

CRISPR-Cas9, a revolutionary genetic editing tool that allows scientists tochange the DNA code of an organism, has quickly become one of the most important medical advancements of our time. Theoretically, the possibilitiesof what can be done with targeted genetic editing are immense, and each new innovation gives hope to millions of people with inherited disorders across the globe.

However, like all things in life, CRISPR-Cas9 is not perfect. It sometimes likes tochange bits of DNAthat it shouldnt, and sometimes itis simply not viable for use against a disease.

In an attempt to combat CRISPR-Cas9's limitations, researchers fromtheWeissman Labat the Whitehead Institutehave developed a new CRISPR technology calledCRISPRonandCRISPRoff, which can target specific genes and turn them on or offwithout changing the DNA code. Their findings are published in the journalCell.

The big story here is we now have a simple tool that can silence the vast majority of genes, says Weissman in astatement.

We can do this for multiple genes at the same time without any DNA damage, with great deal of homogeneity, and in a way that can be reversed. It's a great tool for controlling gene expression.

CRISPRoffuses the same fundamental targeting systems as CRISPR-Cas9, hence theirclose names. CRISPR-Cas9 is a two-part system, involving a CRISPR sequence and aCas9protein associated with it. The CRISPR sequence acts as a homing beacon you can target it at a specific point in the genetic code of an organism and it searches out that sequence. Upon arrival, it unleashes Cas9, which attacks the DNAand cuts it with enzymes. Broken apart, the CRISPR-Cas9 then leaves the DNA sequenceto repair itself using its own internal machinery, changing the sequence in the desired way in the process.

But changing a DNA sequence is permanent, and using the body's own internal machinerymakes the process difficult to accurately target. What if we could remove the activity of a gene without fundamentally changing it?

To do so, the researchers turned to gene expression. Throughout the genome, genes are regularly turned on and off using the addition of simple chemical groups this is called epigenetics.Oneimportant epigeneticprocess, calledDNA methylation, involves the addition of a methyl group that essentially blocks the gene from being read by the cell if the gene is hidden, it will notbe turned into a protein and the gene is "silenced".

When this goes wrong, diseases can occur. A number of diseases are linked with this activation or silencing,includingPrader-Willisyndrome,Fragile Xsyndrome, and some cancers.

CRISPRon/offutilizesepigenetic modification to genetically edit DNA, allowingscientists to turn genes "on and off" as they choose. Usingsmall pieces of RNA that guideCRISPRon/offto a target site, thetechnologycanadd or remove methyl groups from specific sites in the gene, modifying their expression.

This change is inherited through cell divisions, making it an invaluable tool for anything from understanding the genome to developing therapies against epigenetic disease.The researchers are now hopeful that their new genetic editing can be used across a range of applications, improving the arsenal of tools scientists now have to fight genetic disorders.

I think our tool really allows us to begin to study the mechanism of heritability, especially epigenetic heritability, which is a huge question in the biomedical sciences, said the first author James Nuez.

View post:
New CRISPR Breakthrough Can Turn Genes On And Off With Ease - IFLScience

The newly added research report by Industry Growth Insights (IGI) on the Global Epigenetics Market is a detailed guide to understand several factors that play a vital role in growth progression. The report is fabricated in such a way that fosters the investment decisions and motivates crucial investment discretion for new businesses looking out for seamless market penetration.

Some of the prominent companies that are covered in this report:

IlluminaThermo Fisher ScientificMerck MilliporeAbcamActive MotifBio-RadNew England BiolabsAgilentQiagenZymo ResearchPerkinelmerDiagenode

*Note: Additional companies can be included on request

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Epigenetics Market Report: Introduction

Report on Epigenetics market is a comprehensive study that deals with the status and the global position and offers DROC analysis for transforming competitive dynamics and different factors driving or restraining industry growth. The Epigenetics market is the most booming and promising sector of the industry. The Epigenetics market trend research process includes the analysis of different factors affecting the industry, with the government policy, competitive landscape, historical data, market environment, present and future trends in the market, upcoming technologies, technological developments, and the technical progress in related industry, and market risks, market barriers, opportunities, and challenges.

Why Choose this Report?

Industry Growth Insights (IGI), which is one of the worlds top market research firms, has released a new report on the Epigenetics market. The report is made with great precision and in a comprehensive manner to help the clients to identify hidden opportunities and gather information about unpredictable challenges in the market. The Epigenetics report highlights vital growth factors, restraints, and trends of the market. The research study offers a wholesome analysis of the critical aspects of the Epigenetics market, including competition, segmentation, geographical progress, manufacturing cost analysis, and price structure. We have provided CAGR, value, volume, sales, production, revenue, and other estimations for the global and regional markets.

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The report also includes the impact of the ongoing global crisis i.e., COVID-19 on the Epigenetics market and how the pandemic is transforming the market performance. The published report is made with the help of a vigorous and thorough research methodology. Industry Growth Insights (IGI) is also famous for its data accuracy and granular market reports. A complete picture of the competitive scenario of the Epigenetics market is offered by this report. The report has an impressive amount of data about the recent product and technological developments in the markets. It has a wide spectrum of analysis regarding the impact of these advancements on the markets future growth, wide-range of analysis of these extensions on the markets future growth.

Objectives of the Report

The market seems to be evenly competitive. To analyze any market with simplicity the market is divided into segments, such as its product types, applications, technology, end-users, etc. Segmenting the market into smaller components makes it easier to analyze the dynamics of the market with more transparency. All the data has been depicted with the help of tables and figures that consist of a graphical representation of the numbers in the form of histograms, bar graphs, pie charts, etc. Another key component that is integrated with the report is the regional analysis to assess the global presence of the Epigenetics market.

Following is the gist of segmentation:

By Applications:

OncologyMetabolic DiseasesDevelopmental BiologyImmunologyCardiovascular DiseasesOther Applications

By Types:

DNA MethylationHistone ModificationsOther Technologies

By Regions:

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Table of Contents:

Executive Summary

Assumptions and Acronyms Used

Research Methodology

Epigenetics Market Overview

Global Epigenetics Market Analysis and Forecast by Type

Global Epigenetics Market Analysis and Forecast by Application

Global Epigenetics Market Analysis and Forecast by Sales Channel

Global Epigenetics Market Analysis and Forecast by Region

North America Epigenetics Market Analysis and Forecast

Latin America Epigenetics Market Analysis and Forecast

Europe Epigenetics Market Analysis and Forecast

Asia Pacific Epigenetics Market Analysis and Forecast

Asia Pacific Epigenetics Market Size and Volume Forecast by Application

Middle East & Africa Epigenetics Market Analysis and Forecast

Competition Landscape

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Industry Growth Insights (IGI) has vast experience in making tailored market research reports in many industry verticals. We also have an urge to provide complete client satisfaction. We cover in-depth market analysis, which consists of generating lucrative business strategies for the new entrants and the emerging players of the market. We make sure that each report is subjected to intensive primary, secondary research, interviews, and consumer surveys before final dispatch. Our company offers market threat analysis, market opportunity analysis, and deep insights into the current market scenario.

We invest in our analysts and take care of them to ensure that we have a full roster of experience and expertise in any field we cover. Our team members are selected for stellar academic records, specializations in technical fields, and exceptional analytical and communication skills. We also provide ongoing training and knowledge sharing to keep our analysts tapped into industry best practices and loaded with information.

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Epigenetics Market to Witness Strong Growth Over 2021-2027 | Key Manufacturers Overview- Illumina , Thermo Fisher Scientific , Merck Millipore , Abcam...

Type 2 diabetes is characterised by elevated blood glucose levels. This can cause complications that lead to damage to the kidneys, nerves, and the retina in eyes. Other complications can lead to heart diseases and diabetic foot ulcers, which eventually require amputation.

Until fairly recently type 2 diabetes was considered a major health issue only in developed countries. But theres been an increase in prevalence in developing countries. This has been attributed to rapid urbanisation, increased fast food consumption and general lack of exercise.

The diabetes crisis is forecast to worsen. According to the International Diabetes Federation, African countries can expect an increase of up to 143% in the number of people with diabetes by 2045. Its latest report shows that South Africa has the highest prevalence of diabetes on the continent, and the highest number of diabetes-related deaths. The countrys diabetes-related expenditure 23% of the total health budget spent on the management of the disease in 2019 is also the highest.

The rise in diabetes cases needs to be curbed to ease the demand on healthcare systems. To achieve this, new and innovative ways of assessing the levels of risk people face from diabetes are needed. These must be specific to populations on the continent.

My colleagues and I are involved in research aimed at integrating genetic mechanisms and risk factors associated with diabetes and its associated complications, specifically in an African setting. In particular, we have done research on diabetes diagnosis. Our research aims to shed light on new avenues for assessing diabetes risk.

Conventional methods of diabetes diagnosis and management include the oral glucose tolerance test and the HbA1c test. But these have serious shortcomings.

The glucose tolerance test is cumbersome and time-consuming. It also requires a person to fast before having blood drawn. They are given a glucose solution and blood samples may then be drawn at different intervals. The aim is to measure how well, or poorly, their body is able to return their glucose levels back to normalcy.

There are also concerns about the overall accuracy of these tests.

For its part, studies have shown that the results of the HbA1c test may be compromised by factors such as age, ethnicity and anaemias.

All this points to the need for novel, and more sensitive approaches to diabetes diagnosis and therapy.

One area of research that appears to offer the promise of a solution is the booming field of epigenetics. This field of study looks at how our behaviours and surrounding environment may induce genetic changes that predispose us to certain diseases.

When it comes to diabetes, microRNAs (miRNAs) have been the talk of the town in the past decade. These molecules control which proteins are developed, and which proteins arent. Abnormal expression of these miRNAs may result in reduced amounts of proteins involved in essential bodily processes, or an overproduction of proteins which may have adverse effects. The underproduction of a miRNA involved in insulin production ultimately leads to reduced insulin levels and uncontrolled glucose levels in the blood.

Emerging evidence suggests that altered expressions of these miRNAs may either precede or play a role in the development of diseases such as type 2 diabetes.

The study of genetic mechanisms such as miRNAs is known as epigenetics. This is an umbrella of various mechanisms revolving around genetic changes that may occur due to our habits and surrounding environment. These adverse genetic changes may subsequently result in increased risk of disease.

Our surroundings and how we live govern our predisposition to developing certain lifestyle-oriented diseases, such as type 2 diabetes. Research focus must shift towards understanding the complex interplay between our genetic make-up and the environments we live in. Doing this will redefine therapies and management of lifestyle diseases and curb their growing prevalence. One such avenue is research in miRNAs.

In a recent study we identified miRNAs specifically two, 30a-5p and 182-5p which are associated with abnormal glucose levels. We screened three separate groups: a control group with normal glucose levels; a prediabetic group of people with intermediate glucose levels; and a group of people with newly diagnosed type 2 diabetes.

We observed higher levels of the miRNAs in the prediabetic and diabetic groups, in comparison to the normal group. There was more of an increase in the prediabetic group versus the normal group. This told us that for some reason, people with early-stage diabetes have higher levels of these miRNAs. This could indicate that this is either a compensatory response by the body to curb the disease progression, or a knock-on effect of disease progression.

Either way, our results showed that measuring the expression of these miRNAs could be used as a tool for potentially identifying people with prediabetes.

Our next question was: How well can miRNA expression analysis perform in identifying prediabetes and full-blown diabetes, in comparison to known and acknowledged tests?

To answer it, we statistically compared the use of the two miRNAs to that of the HbA1c test. The results showed that the miRNA 182-5p outperformed the HbA1c test in distinguishing prediabetes. This demonstrated that the miRNAs, in particular 182-5p, could be considered as potential novel biomarkers in identifying people at risk of developing diabetes early enough for interventions to be implemented.

In the light of advances in epigenetics research, doors are slowly beginning to open when it comes to personalised treatment regimens and disease management. Considering the influence our surrounding environment has on our health, scientists have begun exploring suggestions that treatment approaches specific to population groups in a particular region may be the future, particularly when it comes to lifestyle-oriented diseases.

Our findings are important because they underscore why personalised approaches and interventions offer potential solutions to designing innovative new breakthroughs in medicine. Identifying genetic trends that are specific to our population, such as these miRNAs, may improve overall diagnostics, therapy and management of type 2 diabetes.

This would, in turn, alleviate the pressure on healthcare systems.

Read more:
We're on the hunt for novel ways to assess the risk of type 2 diabetes - The Conversation CA

Introduction

Diabetic nephropathy, now commonly recognized as diabetic kidney disease (DKD), occurs in diabetic patients, especially those with poor long-term glycemic control,1 causing high morbidity and risk of death. As lifestyles and diets have changed in recent years, the global incidence of diabetes mellitus (DM) has increased annually, as reported by the International Diabetes Federation, which estimates that the incidence of diabetes mellitus (DM) will increase to 700 million in 2045.2 Consequently, diabetic kidney disease will increase social financial costs and threaten human health. DKD is defined by changes in the structure and function of the kidneys. The primary renal structural changes in DKD are mesangial matrix expansion, extracellular matrix accumulation, glomerular and tubular basement membrane thickening, and podocyte injury, eventually contributing to glomerulosclerosis and tubulointerstitial fibrosis.3,4 Clinically, microalbuminuria refers to the daily amount of urinary albumin between 30 mg-300 mg, also known as incipient nephropathy.5 Persistent microalbuminuria (>300mg/day) is called macroalbuminuria or overt nephropathy, followed by renal injury, ultimately leading to ESRD.35 The pathogenesis of DKD is multifactorial and involves many mechanisms such as oxidative stress, metabolic disturbance, activation of the renin-angiotensin-aldosterone system (RAAS), production of inflammatory factors, profibrotic transforming growth factor-1 (TGF-1), and genetic susceptibility, among which genetic predisposition explains some diabetic patients who do not properly control their glycemia but do not develop DKD.4,6 While some patients with diabetes still develop DKD even if they maintain good glycemic control,7 growing evidence demonstrates the relationship between epigenetic mechanisms and gene expression associated with diabetic complications,8 stressing the role of epigenetic modifications and metabolic memory in diabetic complications. Current diabetic kidney disease treatment strategies include blood pressure control, glycemic control, weight reduction, and intensive lifestyle interventions.9 The most effective drugs for DKD treatment are the combined use of RAAS blockers and Sodium-glucose cotransporter 2 (SGL2) inhibitors.10,11 However, the implementation of these measures seems not likely to improve longer-term outcomes, for example, the reversal and reduction of DKD progression in many patients. The increasing rates of DKD suggest a further understanding of underlying mechanisms to find better novel therapies for the clinical management of DKD.1214

Over the past decade, epigenetics has expanded rapidly in many fields and participates in the pathophysiology of DKD. Furthermore, environmental stimuli and inflammation are considered to mediate epigenetic mechanisms.15 Environmental factors, such as metabolites, contribute to the development of diabetes and DKD, which could regulate epigenetic status. That is to say, epigenetic modifications may play a critical role in DKD.12,16,17 In recent years, histone post-translational modifications (PTMs) have been reported to involve regulating DKD-related gene expression, such as connective tissue growth factor (CTGF), collagen-1[], and plasminogen activator inhibitor-1 (PAI-1).18,19 However, our knowledge of the magnitude of the relationship for histone modifications at individual gene sites with diabetic kidney disease and the underlying mechanisms is limited. In this review, we summarize current findings of histone modifications and DNA methylation in DKD, mainly highlighting the role of histone acetylation and methylation in DKD.

The term diabetic nephropathy was replaced by diabetic kidney disease (DKD) by the Kidney Disease Outcomes Quality Initiative (KDOQI), in line with the chronic kidney disease (CKD) classification.20 Traditionally, DKD is characterized by diffuse or nodular glomerulosclerosis. DKD has traditionally been recognized as a change in hemodynamics and metabolic disturbance. These changes can activate the expression of metabolic product, cytokines, chemokines, and immune system,21,22 as well as dysregulating signaling pathways, such as the oxidative stress2326 and profibrotic pathways.27,28 Furthermore, endothelial cell apoptosis exposed to sustained hyperglycemia could lead to kidney injury. These circulating renal factors have a cross-talk relationship to accelerate kidney damage and cause irreversible injury. DKD not only destroys the kidney itself but damages other organs, resulting in more serious diabetic comorbidities.

Microenvironmental changes and multidimensional pathology in DKD have updated conventional knowledge. Several different factors can enhance the pathogenic pathway initiated and maintained by hyperglycemia in the kidney. These include haemodynamic factors, including impaired autoregulation, hyperperfusion and hypoperfusion, as well as metabolic factors, including excess fatty acids, carbonyl and oxidative stress, and activation of the reninangiotensinaldosterone system (RAAS).29 These factors by themselves do not cause DKD but promote and enhance common pathogenic mechanisms in the presence of diabetes, including increased levels of growth factors, vasoactive hormones, cytokines and chemokines in the kidney. For example, vascular susceptibility to oxidative stress could be increased by endothelial dysfunction under high glucose condition, then endothelial dysfunction and subsequent microvascular rarefaction could also reduce blood flow, ultimately leading to hypoxia.4 The pathological manifestation of DKD is the accumulation of extracellular matrix in the glomeruli and tubules and the increased deposition of collagen, fibronectin, and laminin in the mesangial matrix, glomerular basement membrane, and tubulointerstitium.30

The conventional view is that the relationship between diabetes and mitochondrial dysfunction and complications are related to the harmful effects of hyperglycemia; however, further recognition of the stimulation of mitochondrial biogenesis and mitochondrial electron transport chain activity is more conducive to the treatment of DKD.23 Advanced technology in metabolomics, bioinformatics, and systems biology tools open a new window to find the mechanism of DKD. Similarly, considerable evidence shows that macrophage accumulation is a feature of kidney injury and it can produce pro-inflammatory factors, reactive oxygen species (ROS), and metalloproteinases, which lead to renal damage.31,32 Many studies have demonstrated that macrophages are closely associated with the decrease in the glomerular filtration rate (GFR) and histological changes.33,34 However, the mechanism of M2 macrophages how to promote renal repair and reduce the progression of DKD remains controversial, which is worthy of further study. Meanwhile, autophagy involved in the pathogenesis of diabetic kidney disease is also well described in the literature,35 which highlights the regulation of autophagy in diabetic kidney disease. Although long after attainment of glycemic control, the incidence of diabetic complications can still be induced by the exposure of target cells in memory to hyperglycemia.3638 The Diabetes Control and Complications Trial (DCCT) indicated that patients with type 1 diabetes in the intensive glycemic control group had a lower rate and severity of complications compared with those in the conventional group,39,40 in the follow-up observational Epidemiology of Diabetes Intervention and Complications (EDIC) study, patients in the initial intensive treatment group sustained to maintain a low risk of complications relative to those on conventional therapy.40 The continuous effects of high glucose on metabolic memory are a major obstacle to the effective management of diabetic complications. Substantial evidences support the role of epigenetic mechanisms in metabolic memory, recommending to target these mechanisms which may provide a new therapy to treat the diabetic complications.

Epigenetic modifications regulate gene expression, not the change in DNA sequences.41,42 They can occur in response to environmental stimuli, including diet, metabolic disorders, exercise, oxidative stress, inflammation, and drugs.41 These changes can be passed down to offspring, but can potentially be reversed. Epigenetic modifications include DNA methylation, histone modifications, and non-coding RNAs. At present, more than 100 kinds of modifications have been described, including methylation, acetylation, phosphorylation, sumoylation, ubiquitylation, citrullination, biotinylation, crotonylation, and ADP ribosylation.

In this report, we briefly introduce the epigenetic regulations that have been studied in kidney disease, especially DKD, and then introduce research and the latest developments in histone modification of acetylation and methylation involved in the pathogenesis of DKD. Non-coding RNA has been extensively reviewed and is beyond the scope of this study.43

DNA methylation, recognized as a silencing marker, involves the addition of a methyl group to the 5-position of cytosines and primarily occurs on 5-cytosines of CpG dinucleotides and to a lesser extent in non-CG contexts.44,45 The function of DNA methylation is highly dependent on the location of the CpG in the genome.46 In general, methylation of DNA at gene promoter areas can repress transcription and gene expression, whereas at gene bodies it can activate transcription and modulate alternative splicing.12

Histones are highly conserved, alkaline, positively charged proteins, that contain core histones (H2A, H2B, H3, and H4) and linker histones (H1 and H5).45,47 Similar structures in the four core histones are characterized by a conserved central motif domain and an unstructured amino-terminal tail. The unit structure components of chromatin, called the nucleosome, consists of DNA wrapped around an octamer of histone proteins, which contains an H3-H4 tetramer and two H2A-H2B dimers.48 The post-translational modification (PTM) of histones is the main mechanism to regulate chromatin structure, commonly occurring on the amino acid residues lysine, arginine, serine, tyrosine, and threonine and ultimately influencing transcriptional activity.49 The enzymes that mediate histone modification including acetyltransferases, methyltransferases are called epigenetic writers; deacetylases and demethylases are called epigenetic erasers; and proteins recognizing acetylated proteins at promoters and enhancers are called epigenetic readers (for example, bromodomain-containing protein 4).5052

Post-translational modifications (PTMs) of histone proteins include lysine acetylation (KAc), lysine methylation (Kme), arginine methylation, serine ubiquitylation, and threonine phosphorylation. To date, lysine (K), arginine (R) in both methylation and acetylation are the most widely researched, and phosphorylation, ubiquitination, and sumoylation have also been described.

Histone acetylation involves histone acetyltransferases (HATs) transferring an addition of an acetyl group to the lysine of core histones. Generally, histone acetylation is enriched at promoters and enhancers of actively transcribed genes but decreased in the suppressed genomic region. As acetyl can reduce the negative charge of DNA and make chromatin more easily accessible to transcription factors (TFs) and their coactivators,53 acetylation of lysine residual histones is usually associated with transcriptionally active genes. Three main HATs families include Gcn5-related N-acetyltransferases (GNATs: GCN5 and PCAF), MYST (MOZ and Ybf2/Sas3), Sas2, Tip60, and p300/CREB-binding protein (CBP). Conversely, histone deacetylation is catalyzed by histone deacetylases (HDACs), and histone deacetylation can regulate transcriptional repression by allowing chromatin compaction. Acetyl groups in lysine residues of histones and non-histone proteins can be removed by HDACs.54 Four classes of HDAC have been identified, Class I (HDACs 1, 2, 3, and 8), Class II (HDACs 4, 5, 6, 7, 9, and 10), Class III (SIRT1-7), and Class IV HDAC (HDAC11), which shares similar conserved residues with Classes I and II HDACs. Class I HDACs are expressed ubiquitously, mainly localizing in the nucleus, and demonstrate high enzymatic activity, whereas Class II HDACs show different expression patterns with tissue-specific roles and localize in the nucleus and cytoplasm.63 Classes, I, II, and IV are dependent on Zn2+, whereas Class III HDACs require NAD+ as a co-factor rather than Zn2+ for their enzymatic functions.55 HDAC inhibitors are ineffective against Class III (SIRT1-7). In general, H3K9ac, H3K14ac, H3K18ac, H3K23ac, and H3K27ac are enriched at promoters of transcriptional genes and contribute to gene expression. The association of histone acetylation in DKD progression has been verified in human renal tissues.5658 H3K9 acetylation (H3K9ac) levels were significantly increased in renal biopsies from patients with DKD.56 CHIP assays obtained from the glomeruli of diabetic mice compared with normal conditions in vivo exhibited increased induction of Pai1 (as pro-fibrotic genes) and p21 were related to the enrichment of H3K9ac and H3K14ac at the two gene transcriptional promoters.59 Overexpression of H3K9/14Ac levels was reported at the CTGF, PAI-1, and FN-1 promoters in kidneys of diabetic mice, which were associated with p300/CBP-mediated histone acetylation.60 The antidiabetic agent metformin, is widely used as a first-line treatment for patients with type 2 diabetes mellitus, and it has been reported metformin improves glucose metabolism by stimulating CBP phosphorylation, then triggers the dissociation of the CREB-CBP-TORC2 transcription complex, leading to reducing gluconeogenic enzyme gene expression.61 A recent study showed that STZ-induced diabetic mice kidney could reduce acetylation of nephrin, while reduction of nephrin acetylation may be alleviated by MicroRNA-29a, thus protecting against hyperglycemia-induced podocyte dysfunction.62 In another study, high glucose-induced hyperacetylation of the redox-regulating protein p66Shc promoter in podocytes with diabetic kidney disease increased protein p66Shc expression. Protease-activated protein C (aPC) reversed hyperacetylation of the p66Shc promoter and decreased mitochondrial ROS formation in podocytes.63 Taken together, these studies indicate an important role of histone acetylation in kidney diseases.

Histone methylation mainly occurs on the amino acid residues of lysine and arginine. Unlike histone acetylation, histone methylation functions as an information marker to store rather than change the charge of histones to disturb its contact with DNA.64 Histone methylation has three different forms, mono-, di-, or trimethyl, for lysine or arginine residues, which increases the complexity of PTMs. Therefore, either gene activation or repression in histone methylation is determined by the extent of methylation as well as different residues modified.65 Generally, H3K4me1/2/3, H3K36me2/3, and H3K79me1/2 are related to transcriptionally active gene regions, whereas H3K9me2/3, H4K20me3, and H3K27me3 are associated with repressive gene regions. H3K4me2 andH3K4me3 are fully enriched at transcriptional promoters, leading to gene expression. In contrast, H3K9me3 and H3K27me3 are enriched at inactive or slicing gene promoters, which could inhibit gene expression.65,66 Lysine methylation (Kme) is catalyzed by histone methyltransferases (HMTs). However, histone lysine demethylases remove methyl groups from histones, resulting in the demethylation of histones. The first histone demethylase was lysine methylase 1 (LSD1), which could specifically remove the methylation of H3K4 and H3K9.67,68 Many lysine demethylases were identified and renamed lysine demethylases (KDMs) due to their different specificity to various histone lysine residues and non-histone proteins.6971 Given the high selectivity of these enzymes to targeted histone residues, HMTs are classified as two types: arginine methyltransferases (PRMTs) and lysine methyltransferases (KMTs). Lysine methyltransferases (KMTs) include two families based on the catalytic sequence, one is the SET domain-containing KMTs (Su(var)39, enhancer of zeste and trithorax), and the other is a non-SET domain, for example, DOT1L. Histone methylation is dynamic, reversible modification that is regulated by HMTs and KDMs.17 Interestingly, HMTs and KDMs possess substrates specific for lysine residues. For example, methylation of H3K36 is specifically mediated by SET2, and the demethylation of trimethyl H3K36 andH3K9 is regulated by JHDM3/JMJD (trimethyl demethylases), whereas H3K36me2 and H3K36me1 are only demethylated by JHDM1A instead of JHDM3/JMJD. Similarly, methylation of H3K27 and H3K79 is mediated by EZH2 and DOT1, respectively.64 Histone methylation has been considered one of the most stable PTMs and considerable evidence has demonstrated that histone methylation plays a key role in contributing to the pathogenesis of DKD in preclinical in vivo and in vitro models. Because HMTs are involved in histone methylation, some of the targeted HMTs, small-molecule modulators, have been used to test the therapeutic effects in experimental kidney disease. Interestingly, in type 1 diabetic rat kidney, a decreased level of H3K9me2 on the Col1a1 gene promoter was observed, accompanied by decreased expression of SUV39H1 (a histone methylase, specifically catalyzed H3K9me2/3), which is involved in the development of diabetic renal fibrosis. In diabetic conditions, decreased expression of SUV39H1 HMTs was also demonstrated by Villeneuve et al72 and Chen et al.73 Additionally, decreased histone H3K9me3 levels at the promoters of some pro-inflammatory or pro-fibrotic genes also contributed to the development of DKD.58,74,75 Lin et al found HG decreased histone H3K9me3 levels at the promoters of the fibronectin and p21WAF1 genes in mesangial cells while accelerating HG-induced cell hypertrophy, which was attenuated by Suv39h1 overexpression.76 A recent study of DKD patients showed the overexpression of SUV39H1 and H3K9me3, with reduced renal inflammation and apoptosis, suggesting that SUV39H1 may be a protective target for the treatment of DKD.77 Further research should be conducted to test whether the overexpression chromatin marker, such as H3K9me3, could be used as a marker indicating the progression of DKD. In two rodents models of type 1 diabetes, OVE26 mice and streptozotocin rats, the levels of H3K4m2, a histone methylation activating mark, are increased, while the levels of H3K27m3, a repressive mark, are reduced in key genes, such as Mcp-1, vimentin and the fibrosis marker Fsp150, suggesting differential kidney gene expression in DKD is associated with aberrant histone methylation.

Histone crotonylation consists of the transfer of crotonyl groups to lysine residues of histones, that similar to acetylation, confers histones with negative charge.51,52 Lysine crotonylation (Kcr) has been considered as the conserved histone post-translational modification in the kidney.51 Nonetheless, the genomic pattern of histone crotonylation differs from histone acetylation.51 Histone crotonylation can activate or repress gene transcription in a gene- and/or environment-dependent manner.51 Recently, a potential role of histone Kcr was described in acute kidney injury (AKI).78 Most recently, the protective part of HDAC inhibitors in kidney diseases may be related to their role in crotonylation regulation, which could promote some nephroprotective genes, such as PGC1 and Sirt-3.79 This opens the door to explore therapeutic strategies based on the modulation of histone crotonylation.

Ubiquitin is a small, highly conserved 76 amino acid protein that can be covalently linked to lysine residues on histone and non-histone target proteins;80 And it targets the proteins for degradation through the ubiquitin proteasome system (UPS). Ubiquitination involves a multistep process mediated by an enzymatic cascade with ubiquitin ligases, including E1 activating enzymes, E2 conjugating enzymes, and E3 ubiquitin ligases. Studies found ubiquitination is widely involved in the occurrence of DN.81 The key step in Nuclear factor-kappa B (NF-B) activation is through ubiquitination of IB and NF-B dissociation, which plays a vital role in the expression of inflammatory cytokines related to DN. As previously reported, ubiquitination is involved in the progression of DN through activating NF-B, TGF- by degrading the related signal proteins. Most recently, a study in vitro and vivo suggested the tripartite motif-containing (TRIM13, a well-defined E3 ubiquitin ligase) promoted ubiquitination and degradation of C/EBP homologous protein (CHOP, associated with renal injury), which attenuated DN-induced collagen synthesis and restored renal function.82 This finding provides new insights into the application of histone ubiquitin in the treatment of diabetic nephropathy. Based on existing literature and studies, additional research is required to expose the hidden targets of histone ubiquitination to prevent DN.

Nephrin, a critical podocyte membrane component, has been shown to activate phosphotyrosine signaling pathways in human podocytes, then reduce cell death induced by apoptotic stimuli. High glucose and diabetes result in upregulation of SH2 domain-containing phosphatase 1 (SHP-1) in podocytes, thereby contributing to nephrin dephosphorylation and podocyte apoptosis.83 Additionally, an increased level of SHP-1 was also found in diabetic mice, causing decreased nephrin phosphorylation, which may lead to diabetic nephropathy. Another enzyme, Nicotinamide adenine dinucleotide phosphate oxidase (NOX) is the source of reactive oxygen species in hyperglycaemia; Especially when phosphorylation of the cytosolic components of NOX, the development of oxidative stress worsens the kidney in a series of stages.84 Accordingly, investigating phosphorylation targets may benefit patients with diabetic kidney disease.

Some studies investigated in peripheral blood cells have included histone modifications in type 2 diabetics.85,86 Additionally, histone modification variations have been shown in human monocytes cultured under high glucose at a genome-wide level.87 However, plasma levels may not reflect their status in tissues and the cell nucleus.88 Therefore, further epigenome-wide studies in tissues from T2D patients are needed, especially in single-cell analyses. In some cases, histone acetylation and methylation are in a similar pattern and it is difficult to discern the specific contribution of each histone modification to gene expression differences.57 Although the overall profile of histone methylation in DKD has not been fully described, there is still information on individual modifications and genes.

Diabetic kidney disease is one of the major complications caused by persistent hyperglycemia.85,89 Inflammation and fibrosis are the two main factors implicated in the development of DKD. In this section, we focus on the roles of histone acetylation and methylation in the regulation of inflammation and fibrosis in DKD. Generally, ROS is considered to activate nuclear factor-kappaB (NF-B), resulting in a series of inflammation responses.90 NF-kB, a transcription factor, is involved in diabetic complications. Bierhaus et al91 confirmed that hyperglycemia induces activation of NF-kB, then activates its downstream target molecules such as adhesion molecules (monocyte chemoattractant protein-1 [MCP-1]),92 also known as chemokines CCL2, which participate in the pathogenesis of DKD. Pro-inflammatory cytokines and adhesion molecules are also activated by NF-kB. ROS-mediated inflammatory signaling regulated by lysine methyltransferase SETD7 was observed in an experiment conducted by He et al.93 Previous work has demonstrated that SET9 promotes ECM deposition in fibrosis.94,95 SET9 is shown to be recruited to the -SMA gene, and SET9 inhibition to treat CKD.96 In diabetic mice, high-glucose conditions increased the expression of Set7 and NF-B; both were related with elevated ROS production.97 These findings suggest that histone modifications mediated by ROS are involved in the inflammatory reaction of DKD. Likewise, high blood glucose levels (>15 mM) of stimuli such as TGF- have been implicated in the pathogenesis of DKD due to the adverse influence in renal cells.98100 A body of evidence has shown that TGF--mediated histone modifications are correlated with the development of DKD.101104

Many studies have demonstrated that under high glucose and TGF-1-induced conditions, profibrotic cytokines associated with diabetic nephropathy can be regulated by histone acetylation. Significant induction of PAI-1 and p21 mRNA in TGF-1 treatment of RMCs was associated with elevated H3K9/14Ac levels and overexpression of CREB-binding protein (CBP) or p300 at PAI-1 and p21 promoters. Meanwhile, high-glucose treatment increased H3K9/14Ac at TGF-1-inducible genes PAI-1 and p21 (the key players in DN) in rat renal mesangial cells. Furthermore, increased expression of PAI-1 and p21 in glomeruli from diabetic mice was also associated with elevated levels of promoter H3K9/14Ac, demonstrating abnormal histone acetylation in gene regulation both in vivo and vitro relevance to DN. A previous experiment in human renal proximal tubular epithelial cells (RPTEC) showed that epithelial-to-mesenchymal transition (EMT) induced by TGF-1 could be suppressed by TSA, an HDAC inhibitor.103

CHIP assays from glomeruli of diabetic mice also showed that increased expression of PAI-1 and p21 was related to the enrichment of H3K9/14Ac at their gene promoters.59 Conversely, co-transfection experiments confirmed that the overexpression of HDAC1 and HDAC5 could suppress TGF--induced gene expression (PAI-1 and p21). These studies suggest a key role of histone acetylation in the pathogenesis of gene expression and provide further therapeutic targets for DKD. In another study with a type 1 diabetes mouse model, significantly increased levels of connective tissue growth factor (CTGF), plasminogen activator inhibitor (PAI-1), and fibronectin (FN-1) in the kidney were related to increased HAT activity and enrichment of H3K9/14Ac and HAT p300/CBP at the CTGF, PAI-1, and FN-1 gene,60 suggesting a relationship between histone acetylation and renal fibrosis, which may provide a precise mechanism of glomerulosclerosis and interstitial fibrosis to prevent the development of DKD. It is well established that DKD is characterized by the accumulation of extracellular matrix (ECM) proteins including collagen, laminin, and fibronectin. Some evidence shows that the transcription of ECM proteins is regulated by epigenetic histone modifications. Fibroblasts incubated with TGF- revealed that elevated histone acetyltransferase activity of p300 and histone H4 acetylation accelerated COL1A2 expression.105 Interestingly, research in mice with diabetic kidney disease showed that high glucose induces the expression of myocardin-related transcription factor A (MRTF-A), which could activate collagen transcription. Further analysis revealed that MRTF-A recruited p300 and WD repeat-containing protein 5 (WDR5), an important component of histone H3K4 methyltransferase, to the collagen promoters, eventually leading to its gene expression.106 MRTF-A silencing makes acetylated histone H3K18/K27 and trimethylated histone H3K4 disappear and diminishes diabetic tubulointerstitial fibrosis.107 This study indicates that MRTF-A-associated histone modifications might provide a novel mechanism against DN-associated renal fibrosis. In another study, mice with streptozotocin-induced diabetic kidney disease showed low expression of the histone deacetylase SIRT1, and increased albuminuria. However, overexpression of SIRT1 in renal tubular could induce hypermethylation of the Cldn1 gene (the tight junction protein) and then prevented albuminuria.108 On the other hand, proximal tubule-specific deletion of Sirt1 in mice showed increased albuminuria related with reduced Cldn1 methylation, increased histone acetylation, and upregulation of Claudin-1.108 Thus, it can alleviate renal fibrosis with reduced albuminuria. These studies show the protective effects of SIRT1 in DKD and can further as a therapeutic target for DKD with in-depth evaluation. In rat DKD, the HDAC inhibitors trichostatin A (TSA) and valproic acid (VPA) were protective. TSA blocked extracellular matrix accumulation by TGF-1-induced. And it is thought to increase E-cadherin expression through HDAC inhibition, leading to increased acetylation of E-cadherin promoter, but it is unclear the mechanism on TGF-1 expression.102 HDAC 2/4/5/9 have been shown to be upregulated in kidney biopsy tissue obtained from patients with diabetes. More specifically, the mRNA level of HDAC2/4/5 was negatively correlated with eGFR in patients with DKD. Noh et al102 also reported that markedly increased HDAC-2 activity was proved in kidneys of diabetic rats and rat tubular epithelial cells. New observations demonstrate diabetes and TGF-1 could activate HDAC-2 in the kidneys, eventually involving the accumulation of ECM and EMT, and EMT has been reported to cause podocyte loss.109111 Podocytes stimulated by harmful factors such as high glucose, advanced glycation end products, and transforming growth factor- showed high expression of HDAC4. However, renal injury was alleviated by silencing the HDAC4 gene.112 After in-depth studies, Wang et al reported that inhibition of autophagy and increasing renal inflammation were associated with the effects of HDAC4112. In vivo gene silencing of HDAC4 ameliorated renal injury in STZ-induced diabetic rats, as evidenced by reduced albuminuria, ameliorated podocyte injury and mesangial expansion.113 Hence, HDAC4 plays a critical role in regulating the pathogenesis of DKD as an epigenetic mediator. Cultured murine proximal tubular cells treated with TGF-1 also showed protective effects through treatment with PCI34051 (a highly selective inhibitor of HDAC8) or HDAC8 siRNA, suppressing EMT.114 All of the above indicates that HDAC changes influence the progression of DKD, which may promote renal fibrosis and EMT. In view of individual HDAC isoforms playing different roles, additional studies are needed to clarify the relationship between renal fibrosis and histone acetylation and deacetylation, further giving a therapeutic target for individual patients with DKD.

In the Diabetes Control and Complication Trial (DCCT), the progress of microvascular results in the long-term Epidemiology of Diabetes Intervention and Complication (EDIC) studies showed that the hyperacetylation promoter (P < 0.05) in the top 38 cases contained more than 15 genes related to the NF-B inflammatory pathway and rich in genes related to diabetic complications.114 Preliminary work in endothelial cells showed that the sustained expression of p65 was associated with enrichment in Set7 and H3K4me1 on the p65 gene promoter, although cultured in transient hyperglycemia, and changes will always exist, even if returning to normoglycemia.71,115 The study highlighted that short-term hyperglycemia could have long-lasting effects on gene expression through epigenetic histone modification. Evans et al116 reported that stress-activated protein kinases stress pathways such as the NF-B, p38 MAPK, and kinases resulted in late diabetic complications. The first study of human blood monocytes showed that, under diabetic conditions, increased levels in acetylation of histones H3K9/14Ac and H4K5, 8, and 12Ac at the promoters of inflammatory genes such as TNF- and COX-2 led to gene transcription.117 Another study in advanced diabetic kidney disease mice after unilateral nephrectomy showed significantly increased global renal histone H3K9 and H3K23 acetylation, whereas CCL2 antagonist not only reversed histone acetylation abnormalities but also alleviated the progression of diabetic kidney disease.57 These studies demonstrated that histone acetylation under diabetic conditions is involved in the pathogenesis of DKD, which was associated with the continuous expression of the inflammatory gene. HDAC1 is downregulated both in Akita mice and in rat glomerular mesangial cells exposed to high glucose, resulting in overexpression of inflammatory gene through histone hyperacetylation.118 In another study, elevation of RNA polymerase II recruitment and H3K4me2 was found but decreased repressive H3K27m3 markers at the MCP-1 gene were observed in an OVE26 mice model of T1DM instead of in rat models, which eventually contributed to the increased expression of MCP-1 in a mouse model.119 The difference between rats and mice suggests that individual differences in epigenetics also need to be taken into account when translating into human DKD.

Under normal and high-glucose conditions, histone methylation is associated with TGF--1-mediated ECM gene expression, such as Colla1, plasminogen activator inhibitor-1 (PAI-1), and connective tissue growth factor (CTGF).120123

TGF-1 plays an important role that drives collagen myofibroblasts in injured kidneys and their signaling is also a key mediator in the expression of fibrotic and ECM genes involved in the pathogenesis of diabetic kidney diseases. In models of TGF-1-induced renal fibrosis, hypermethylation of Rasal1 promoter was induced by TGF-1, which increased fibroblast activation, and fibrosis.108 In another study of 18 in RMCs stimulated by TGF-1 showed not only the increasing recruitment of H3K4, HMT, and SET7/9 at ECM gene promoters but also in the expression of SET7/9. However, knockdown of SET7/9 could decrease global H3K4me1 but not H3K4me2 or H3K4me3 levels, indicating SET7/9-mediated H3K4me1 could play an important role in ECM gene expression. Involvement of histone methyltransferase (HMT) SET7/9 in p21 gene expression related to cellular hypertrophy, which results in the pathogenesis of DN, has also been demonstrated both in glomeruli of STZ-induced rats and HG-induced RMCs.124 These studies suggest that SET7/9 could participate in renal fibrosis by regulating methylation of H3 lysine 4 at fibrotic gene promoters. Then, SET7/9 may be a potential target for fibrotic gene disorders, which could provide potential therapeutic targets for DKD.

H3K9me3 levels in vascular smooth muscle cells (VSMCs) and endothelial cells in diabetic db/db mice were lower than those in a control db/db group.125,126 They were consistent with the result of a study of RMCs stimulated by TGF-1, which were related to HG-induced upregulation of these fibrotic genes. It was found that in patients with diabetic kidney disease, H3K9me3 overexpression in renal tubules has been verified as a protective role by decreasing renal inflammation and apoptosis. Accordingly, more details should be researched in DKD with the methylation of H3K9 for new insights to delay the progression of DKD. Loss of H3K27me3, EZH2, and heightened UTX (also known as KDM6A, a histone demethylase) were detected in the human podocytes in glomeruli of DKD, which increased podocyte dedifferentiation and aggravated glomerular injury by regulating Jagged-1 overexpression.127 Increased expression of H3K27me3 demethylases accompanied by decreased levels of Ezh2 protein and H3K27me3 were observed in rodent models with diabetic kidney disease. In the same experiment, RMCs stimulated by TGF- showed that the reduction of H3K27me3 at the CTGF, Serpine1, and CCl2 gene promoters upregulated profibrotic and inflammatory gene expression.101 Moreover, in streptozotocin-diabetic rats and in podocytes cultured under a high glucose with the inhibition of EZH reduced H3K27me marks at the Pax6 promoter, and then promoting PAX6 expression and aggravating podocyte injury, oxidative stress and proteinuria.128 However, another report showed that high-glucose stimulation promoted EMT and significantly up-regulated EZH2 expression in renal tubular epithelial cells, which may participate in the development of DN.129 The existence of the above biases may be related to the balance of histone methylation in epigenetic processes. SUV39H1, another histone methyltransferase as repressive mark H3K9m3, has been observed downregulated in kidneys from streptozotocin mice and in mesangial cells under high glucose. Interestingly, overexpression of SUV39H1 decreased extracellular matrix production in mesangial cells, reducing the renal fibrosis.76,130

In experimental diabetic nephropathy, histone methylation was associated with severe glomerulosclerosis, albuminuria and glomerular filtration rate reduction and CCL2 antagonist prevented the histopathological damage, indicating a role for CCL2 or inflammation in epigenetic regulation.57

In vitro, endothelial cells cultured in transient hyperglycemia showed that an increase in p65 expression was correlated with elevated levels of H3K4me1 and SET7 at the p65 promoter, but there was no change in H3K4me2/3.115,126 In the same study, EI-Osta et al115 indicated that sustained increase in monocyte chemoattractant protein 1 (MCP-1) and vascular cell adhesion molecule 1 (VCAM-1) were induced by activation of p65, both involved in the pathological process of DKD. HMT SET7 (the H3K4 methyltransferase) promotes the expression of inflammatory genes such as TNF-alpha in monocytes, which is a downstream inflammatory factor regulated by NF-B.131 These findings revealed the key role of HMT involved in mediating the expression of inflammatory genes related to DKD. Diminished H3K27me3 and increased expression of UTX were observed in glomerular podocytes from humans with glomerulosclerosis or DKD, whereas inhibition of UTX alleviated the established glomerular injury in db/db mice; UTX was recently found overexpressed in DKD patients and an elevated level of UTX and reduced H3K27me2/3 were also observed in db/db mice. Further studies to reveal the role of UTX in DKD showed that the transcriptional activation of inflammatory genes is mediated by UTX through removing H3K27me3 from these gene promoters.131 These results suggest the pathogenesis of DKD is associated with histone methylation and inflammation in the process could be regulated by histone methylation. Although TGF- is considered the key cytokine in contributing to fibrosis,132 the suppressed expression of matrix metalloproteinase 9 (MMP9) could also alleviate pathological conditions of early diabetic kidney disease,133 such as mesangial expansion, proteinuria, and podocyte foot effacement in the early stage of diabetic kidney disease. The decreased expression of lncRNA growth arrest-specific transcript5 (GAS5) and matrix metalloproteinase 9 (MMP9), a key inflammatory protein associated with DKD pathogenesis, was shown in a rat model with diabetic kidney disease. ChIP assays demonstrated that dramatic enrichment of EZH2 (a methyltransferase that induces histone H3 lysine 27 trimethylation) after overexpression of GAS5 could also elevate H3K27me3 as well as EZH2 to the promoter region of MMP9, leading to downregulated MMP9 expression and attenuating early diabetic kidney injury.134 The experimental data provide a promising target for DKD in the GAS5/MMP9 regulatory mechanism. EZH2 treatment can also impede the progression of DN. However, elevated recruitment of RNA polymerase II and H3K4me2 but decreased repressive H3K27m3 markers at MCP-1 genes were observed in a mouse model of T1DM instead of in male Sprague-Dawley rat models, which eventually contributed to increased expression of Monocyte chemoattractant protein-1 (MCP-1) in a mouse model.119 The difference between rats and mice suggests that individual differences in epigenetics also need to be taken into account when translating into human DKD.

A single histone modification does not always function in isolation. There is a complex interplay of indistinct histone modification. As previously mentioned, increased expression of pro-fibrotic genes (Colla1, PAI-1, and CTGF) induced by TGF1 and high glucose were enriched with active histone methylation markers, H3K4me, and histone acetylation markers H3K9/14ac at their promoters, hence their co-modifications may lead to more transcription of pro-fibrotic genes. Similarly, H3K18/K27ac and H3K4me3 recruited to the collagen promoters participate jointly in renal fibrosis of DKD.107 In other DKD experimental mice, increased histone acetylation (H3K9 and H3K23) and histone methylation (H3K4 dimethylation) were associated with progressive glomerulosclerosis,57 so these co-expressed chromatin markers can provide a useful signal to indicate advanced diabetic nephropathy, which could support clinicians to provide individualized treatment for patients. Considerable evidence has suggested that injured kidneys increased the expression of DOT1L and H3K79 dimethylation, particularly in renal tubular epithelial cells and myofibroblasts, eventually aggravating renal fibrosis, even developing end-stage renal disease. However, emerging evidence by Zhang et al135 showed that Dot1l has an antifibrotic effect. Using several approaches in groups of mice, Dot1a-HDAC2 complex regulated H3K79me2 and H3 acetylation at the endothelin 1 (Edn1) promoter, ensuring the balance of endothelin transcription. This could represent a new mechanism between Dot1a and HDAC2 in modulating kidney fibrosis.

Some epigenetic drugs focus on cancer, neuronal diseases, hematological diseases and inflammatory disease,136,137 such as HDAC inhibitors.138 HDAC inhibitors were used for the modulation of insulin signaling and -cell functioning,139,140 as it could release the glucose transporter 4, GLUT4,141 and then transfers the glucose from the outside cell to the inside of the cell, avoiding producing a series of harmful factors to the kidney. The class III HDAC protein, SIRT1, plays a protective role in the upregulation of the antioxidant gene in glomerular mesangial cells.142 In diabetic OVE26 mice, administration of the SIRT1 agonist BF175 attenuated podocyte injury.143 However, HDAC inhibitors were generally non-specific; Hence, it may be valuable to develop more selective inhibitors or activators of HDACs. Meanwhile, considering safety and specific populations that may benefit from epigenetic interventions, there is not yet enough information. Accordingly, more clinical trial stages should be target epigenetic modifications in DKD. The most tough and unresolved but critical issue is to define the tissue-specific relative contributions of epigenetic writers and erasers; It has been shown HDAC3 deletion from the macrophage is vasculo-protective,144 while deletion of the HDAC3 from endothelial cells aggravates the macrovascular disease.145 Recently, whereas HDAC9 is a protective target for Medial artery calcification (MAC) in CKD patients,146 overexpression of the same enzyme in diabetic nephropathy exacerbates podocyte injury.147 In the future, Genome editing via CRISPRCas9 and other methods148151 will be a strong method to modify epigenetic changes, benefiting from its locus-specific epigenetic modification, eventually improve the efficacy of pharmacological therapy.

The pathogenesis of DKD is complicated with interactions between injury factors, growth factors/cytokines, and metabolic products. The epigenetic mechanism can integrate these connections to mediate the development of DKD. With accumulating investigations in both animals and renal cells, as well as the data from clinical diabetes patients, as previously described, we can conclude that metabolic memory exists in DKD. Histone modifications and DNA methylation participate in DKD-associated gene expression, including fibrotic and inflammatory genes (Figure 1). The epigenetic mechanism provides an insight to thoroughly understand the DKD mechanism. Cellular heterogeneity and individual differences were found in histone modifications, so the cell-type-specific gene expression affected by histone modifications makes it difficult to identify the stage of DKD progression in clinical patients, even using epigenome-wide association studies (EWAS). Overall, HDAC inhibitors may protect against fibrosis in diabetic kidney disease. However, this field remains challenging, since the enzymes have a broad substrate specificity and deacetylate many proteins that are not related to epigenetic regulation.136 Although these data indicate that histone acetylation and methylation may play a key role in altered gene expression during DKD, it is more necessary to specifically target individual enzymes function in vivo. The detailed analysis of DKD between histone modifications requires more in-depth research. For example, high glucose may induce more transcriptional factors that regulate DKD-associated genes with epigenetic histone modifications. Understanding the regulation of fibrosis by TGF- can help identify more potential antifibrotic targets, which could prevent or halt renal fibrosis in DKD. Exploring the precise pathological mechanisms in epigenetic histones and novel biomarkers is necessary to translate these preclinical findings into treatment strategies for DKD patients. Also, when single-cell epigenetic techniques are developed and together with currently available single-cell transcriptomics data, it can pinpoint the effect of certain histone post-translational modifications to a specific cell type or a specific molecule.

Figure 1 Schematic representation of histone modifications in diabetic-induced fibrotic and inflammatory gene expression. High-glucose conditions cause the expression of ECM-associated genes Col1a1, CTGF, PAI-1, FN-1, Lacm1, and P21 as well as inflammatory genes TNF-, COX-2, and MCP-1, leading to fibrosis and glomerulosclerosis in the pathogenesis of DKD. The gene expression is based on the increased active chromatin markers (H3K4me, H3K9/14ac, and H3K79me) and decreased repressive markers (H3K9me3 and H3K27me3) on the promoters of fibrotic and inflammatory genes. Under diabetic conditions (high glucose), TGF- antibodies, some specific HDACs, TSA, and antioxidants could have renoprotective effects.

All authors contributed to data analysis, drafting or revising the article, have agreed on the journal to which the article will be submitted, gave final approval of the version to be published, and agree to be accountable for all aspects of the work.

This study was funded by research grants (81870500 and 81770692) from the National Natural Science Foundation of China. It was also supported by the Hunan Provincial Clinical Medical Technology Innovation Guide Project (S2020SFYLJS0334).

The authors report no conflicts of interest in this work.

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[Full text] Epigenetic Histone Modifications in the Pathogenesis of Diabetic Kidne | DMSO - Dove Medical Press

While eyesight often dims with age, a novel mouse study provides intriguing evidence that innovative gene therapy techniques could someday roll back the biological clock for our vision. The research was conducted with NIA and the National Eye Institute support by a Harvard Medical School team and published recently in Nature.

The teams approach involved epigenetics, a field of science that studies heritable changes that can activate or deactivate genes without any change in the underlying DNA sequence of these genes. The word epigenetics is of Greek origin and literally means over and above (epi) the genome.

Their experiments refined a technique that won a Nobel prize in 2012. The basic idea is that by using a harmless virus to introduce just a few genes, called Yamanaka factors after the researcher who discovered them, scientists can reprogram the DNA of mature cells of different types to transform back into young (pluripotent) stem cells. These can then regenerate function lost to age, illness, or injury. The virus payload is turned on or off via injection of a selective inducer molecule.

This cell reprogramming method could lead to future disease therapies, but previous studies showed it is tough to safely rein in the rapid cell growth and tumor development triggered by Yamanaka factors. The Harvard team found a way to keep the beneficial effects and weed out the dangerous ones by leaving out one of the four factor genes, called MYC, that is closely related to cancer and can shorten the lifespan of mice when it is expressed.

First working in lab cell cultures, the team was able to rejuvenate damage to retinal ganglion cells, a type of neuron found at the rear of the eye. Later in a mouse model, the same techniques seemed to protect some optic nerve cells from damage and caused others to grow fresh connections to the brain. A third experiment had similar success reversing some vision damage in a mouse model of glaucoma, a leading cause of age-related blindness in humans.

In lab tests, the glaucoma model mice who received the injection treatment gained back roughly half of their previously lost visual ability. In other experiments, middle-aged mice who received the injection scored similar to younger mice in visual tests, plus their DNA showed expression and methylation (epigenetic patterns of common chemical groups that attach to DNA at different life stages) signatures that resembled the genetic material of younger mice. They have also found that these recovered functions require two DNA methylation enzymes that could be responsible for these epigenetic changes during the reprograming.

While the researchers are encouraged by this progress, they caution that epigenetic reprogramming techniques are still very complex and still harbor risk of abnormal cell growth or cancer. They plan to conduct many further studies to test the gene therapy technologies in larger animals, explore how the restorative factors impact other types of cells and tissues, and verify that the youthful changes seen are not fleeting.

This research was funded by NIA grants R01AG019719, R37AG028730, R01AG067782, R01AG065403, K99AG068303, and T32AG023480.

Reference: Lu Y, et al. Reprogramming to recover youthful epigenetic information and restore vision. Nature. 2020;588(7836):124-129. doi:10.1038/s41586-020-2975-4

Originally posted here:
Gene therapy techniques restore vision damage from age and glaucoma in mice - National Institute on Aging

GLOBAL EPIGENETICS-BASED INSTRUMENTS MARKETIS EXPECTED TO REGISTER A SUBSTANTIAL CAGR IN THE FORECAST PERIOD OF 2019-2026. THE REPORT CONTAINS DATA FROM THE BASE YEAR OF 2018 AND THE HISTORIC YEAR OF 2017. THIS RISE IN MARKET VALUE CAN BE ATTRIBUTED TO THE VARIOUS INNOVATIONS AND ADVANCEMENTS OF TECHNOLOGIES ASSOCIATED WITH EPIGENETICS.

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