DNA methylation and gene silencing in cancer.

Stephen B Baylin
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引用次数: 1140

Abstract

Epigenetic changes such as DNA methylation act to regulate gene expression in normal mammalian development. However, promoter hypermethylation also plays a major role in cancer through transcriptional silencing of critical growth regulators such as tumor suppressor genes. Other chromatin modifications, such as histone deacetylation and chromatin-binding proteins, affect local chromatin structure and, in concert with DNA methylation, regulate gene transcription. The DNA methylation inhibitors azacitidine and decitabine can induce functional re-expression of aberrantly silenced genes in cancer, causing growth arrest and apoptosis in tumor cells. These agents, along with inhibitors of histone deacetylation, have shown clinical activity in the treatment of certain hematologic malignancies where gene hypermethylation occurs. This review examines alteration in DNA methylation in cancer, effects on gene expression, and implications for the use of hypomethylating agents in the treatment of cancer.

癌症中的DNA甲基化和基因沉默。
表观遗传变化,如DNA甲基化,调节正常哺乳动物发育过程中的基因表达。然而,启动子超甲基化也通过转录沉默肿瘤抑制基因等关键生长调节因子在癌症中发挥重要作用。其他染色质修饰,如组蛋白去乙酰化和染色质结合蛋白,影响局部染色质结构,并与DNA甲基化一起调节基因转录。DNA甲基化抑制剂阿扎胞苷和地西他滨可以诱导肿瘤中异常沉默基因的功能性再表达,导致肿瘤细胞生长停滞和凋亡。这些药物与组蛋白去乙酰化抑制剂一起,在治疗某些发生基因高甲基化的血液恶性肿瘤中显示出临床活性。本文综述了癌症中DNA甲基化的改变,对基因表达的影响,以及在癌症治疗中使用低甲基化药物的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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