生物
表观遗传学
癌症研究
组蛋白甲基转移酶
三阴性乳腺癌
癌症表观遗传学
EZH2型
表观遗传疗法
组蛋白
癌变
甲基转移酶
乳腺癌
癌症
遗传学
DNA甲基化
甲基化
基因
基因表达
作者
Janice Jacson Mandumpala,Stephin Baby,Antriya Annie Tom,Chandraiah Godugu,Nagula Shankaraiah
出处
期刊:Life Sciences
[Elsevier]
日期:2022-03-01
卷期号:292: 120321-120321
被引量:13
标识
DOI:10.1016/j.lfs.2022.120321
摘要
Triple-negative breast cancer (TNBC) is a particularly lethal subtype of breast cancer owing to its heterogeneity, high drug resistance, poor prognosis and lack of therapeutic targets. Recent insights into the complexity of TNBC have been explained by epigenetic regulation and its ability to modulate certain oncogenes and tumour suppressor genes. This has opened an emerging area in anti-cancer therapy using epigenetic modulating drugs, highlighting the epigenetic reprogramming during tumorigenesis and tumour development. Histone methylation and demethylation are such dynamic epigenetic mechanisms mediated by histone methyltransferases (HMTs) and histone demethylases (HDMs), respectively. The interplay between HMTs and HDMs in histone methylation extrapolates their viability as druggable epigenetic targets in TNBC. In this review, we aim to summarize recent progress in the field of epigenetics focusing on HMTs and HDMs in TNBC development and their potential use in targeted therapy for TNBC management.
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