Role of DNA methylation in cancer development and its clinical applications

Swarup Sonar, Sidhanti Nyahatkar, Ketki Kalele, Manab Deb Adhikari
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Abstract

methyltransferase gene (DNA) methylation is a key process in epigenetic modification. This transformation leads to genomic instability that creates an impact on gene expression. DNA methylation is also involved in several mutations of tumour suppressor genes (TSGs) or proto-oncogenes, resulting in cancer (hypermethylation and hypomethylation). Hypermethylation of promoter segments in TSGs causes transcriptional silencing, whereas hypomethylation of regulatory sequence activates proto-oncogenes and retrotransposons. DNA methylation regulated by DNA methyltransferases is one of the essential epigenetic mechanisms that controls the cell cycle, cell proliferation, differentiation, apoptosis and transformation in eukaryotes, leading to genetic instability of tumour cells. Recent scientific research has highlighted that DNA methylation is a vital cancer biomarker source of several parts of body fluids that allow primary-stage cancer cell detection during clinical screening. Nowadays, epigenetic biomarkers have been introduced as a decision maker with the potential to improve cancer prognosis. DNA methylation profiling helps to determine cancer at the deep genetic level, and create high impactful cancer screening approach in the future.

Abstract Image

DNA 甲基化在癌症发展中的作用及其临床应用
甲基转移酶基因(DNA)甲基化是表观遗传修饰的一个关键过程。这种转变导致基因组不稳定,对基因表达产生影响。DNA 甲基化还与肿瘤抑制基因(TSG)或原癌基因的一些突变有关,从而导致癌症(高甲基化和低甲基化)。TSGs 启动子片段的高甲基化会导致转录沉默,而调控序列的低甲基化则会激活原癌基因和转座子。由 DNA 甲基转移酶调控的 DNA 甲基化是控制真核生物细胞周期、细胞增殖、分化、凋亡和转化的重要表观遗传机制之一,导致肿瘤细胞的遗传不稳定性。最近的科学研究突出表明,DNA 甲基化是体液中多个部位的重要癌症生物标记源,可在临床筛查中进行初级阶段的癌细胞检测。如今,表观遗传生物标志物已被引入作为一种决策制定工具,具有改善癌症预后的潜力。DNA 甲基化分析有助于在深层基因水平上确定癌症,并在未来创造出具有高度影响力的癌症筛查方法。
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