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Nachuan Zhang

Bio: Nachuan Zhang is an academic researcher from Life Sciences Institute. The author has contributed to research in topics: DNA methylation & Epigenetics. The author has an hindex of 1, co-authored 1 publications receiving 6 citations.

Papers
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Book ChapterDOI
TL;DR: This chapter focuses on the general introductions of epigenetics, which is important in the regulation of chromatin structure and gene expression, and various mutations of epigenetic regulators have been identified and proven to be the drivers of tumorigenesis.
Abstract: Epigenetics is the epi-information beyond the DNA sequence that can be inherited from parents to offspring. From years of studies, people have found that histone modifications, DNA methylation, and RNA-based mechanism are the main means of epigenetic control. In this chapter, we will focus on the general introductions of epigenetics, which is important in the regulation of chromatin structure and gene expression. With the development and expansion of high-throughput sequencing, various mutations of epigenetic regulators have been identified and proven to be the drivers of tumorigenesis. Epigenetic alterations are used to diagnose individual patients more accurately and specifically. Several drugs, which are targeting epigenetic changes, have been developed to treat patients regarding the awareness of precision medicine. Emerging researches are connecting the epigenetics and cancers together in the molecular mechanism exploration and the development of druggable targets.

133 citations


Cited by
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Journal ArticleDOI
01 Aug 2022-Cells
TL;DR: The roles of mitochondria in key metabolites required for epigenetics modification and in cell fate regulation are summarized and the current strategy in cancer therapies via targeting epigenetic modifiers and related enzymes in metabolic regulation is discussed.
Abstract: Mitochondria are not only the main energy supplier but are also the cell metabolic center regulating multiple key metaborates that play pivotal roles in epigenetics regulation. These metabolites include acetyl-CoA, α-ketoglutarate (α-KG), S-adenosyl methionine (SAM), NAD+, and O-linked beta-N-acetylglucosamine (O-GlcNAc), which are the main substrates for DNA methylation and histone post-translation modifications, essential for gene transcriptional regulation and cell fate determination. Tumorigenesis is attributed to many factors, including gene mutations and tumor microenvironment. Mitochondria and epigenetics play essential roles in tumor initiation, evolution, metastasis, and recurrence. Targeting mitochondrial metabolism and epigenetics are promising therapeutic strategies for tumor treatment. In this review, we summarize the roles of mitochondria in key metabolites required for epigenetics modification and in cell fate regulation and discuss the current strategy in cancer therapies via targeting epigenetic modifiers and related enzymes in metabolic regulation. This review is an important contribution to the understanding of the current metabolic-epigenetic-tumorigenesis concept.

44 citations

Journal ArticleDOI
TL;DR: In this article , a review aimed to elaborate on the interactions among diet, gut microbiota, and epigenetics to uncover the mechanisms and therapeutics of metabolic diseases, including obesity, dyslipidemia, type 2 diabetes mellitus (T2DM), and non-alcoholic fatty liver disease (NAFLD).

22 citations

Journal ArticleDOI
TL;DR: Based on its structure and compaction state, chromatin is categorized into euchromatin, heterochromatin and centromeric chromatin this article, and molecular complexes are classified into three groups based on their role in both packaging DNA and regulating DNA metabolic pathways such as DNA replication, transcription, recombination, and chromosome segregation.
Abstract: Chromatin consists of a complex of DNA and histone proteins as its core components and plays an important role in both packaging DNA and regulating DNA metabolic pathways such as DNA replication, transcription, recombination, and chromosome segregation. Proper functioning of chromatin further involves a network of interactions among molecular complexes that modify chromatin structure and organization to affect the accessibility of DNA to transcription factors leading to the activation or repression of the transcription of target DNA loci. Based on its structure and compaction state, chromatin is categorized into euchromatin, heterochromatin, and centromeric chromatin. In this review, we discuss distinct chromatin factors and molecular complexes that constitute euchromatin—open chromatin structure associated with active transcription; heterochromatin—less accessible chromatin associated with silencing; centromeric chromatin—the site of spindle binding in chromosome segregation.

22 citations

Journal ArticleDOI
TL;DR: In this article , the authors tracked old and new histones throughout the male germline stem cell (GSC) cell cycle through the use of high spatial and temporal resolution microscopy, and found unique features that differ between old and newly enriched sister chromatids, including differences in nucleosome density, chromosomal condensation, and H3 Ser10 phosphorylation.

15 citations

Journal ArticleDOI
TL;DR: Wang et al. as discussed by the authors designed, synthesized and verified a series of 1,3-diaryl-1,2,4-triazole-capped histone deacetylase 6 (HDAC6) inhibitors with promising anti-gastric cancer activities.

13 citations