表观遗传学
癌变
药物发现
DNA甲基化
组蛋白
表观遗传疗法
EZH2型
癌症
生物
药物开发
癌症研究
临床试验
生物信息学
医学
计算生物学
药品
基因
药理学
基因表达
遗传学
出处
期刊:Anti-cancer Agents in Medicinal Chemistry
[Bentham Science]
日期:2016-04-14
卷期号:16 (6): 699-712
被引量:5
标识
DOI:10.2174/1871520616666151116124432
摘要
In recent years, there has been an expansion of the understanding of how epigenetic dysregulation plays a role in tumorigenesis, progression, metastasis and treatment resistance. Evidence has focused on two common and well-studied "epigenetic codes", i.e., DNA methylation and histone posttranslational modification, which regulate the transcriptional status in various types of cancer and the corresponding target agents. Aside from "writers" and "erasers", which refer to enzymes that catalyze and remove posttranslational modifications, respectively, "readers" bind to target proteins and recruit "writers" and "erasers" for regulating gene expression. A number of selective and potent anticancer compounds have been reported, some of which are in preclinical or clinical trials that have shown promising results, primarily against malignant neoplasms such as hematologic malignancies, with the subsequent emerging development of both monotherapy and co-administration with traditional cytotoxic medicines against solid tumors. Second-generation epigenetic agents such as EZH2 and BET inhibitors have greatly progressed. Epigenetic dysregulation has also provided feasibility for the diagnosis and treatment of cancer. In this review, we summarize the progress in epigenetics and drug discovery for cancer and certain clinical trials that may provide a perspective for future development.
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