脱甲基酶
生物
组蛋白
组蛋白甲基化
组蛋白甲基转移酶
染色质
表观遗传学
甲基转移酶
癌症研究
EZH2型
细胞生物学
甲基化
计算生物学
DNA甲基化
遗传学
基因表达
DNA
基因
作者
Amir Hosseini,Saverio Minucci
出处
期刊:Epigenomics
[Future Medicine]
日期:2017-08-01
卷期号:9 (8): 1123-1142
被引量:115
标识
DOI:10.2217/epi-2017-0022
摘要
Histone methylation plays a key role in the regulation of chromatin structure, and its dynamics regulates important cellular processes. The investigation of the role of alterations in histone methylation in cancer has led to the identification of histone methyltransferases and demethylases as promising novel targets for therapy. Lysine-specific demethylase 1(LSD1, also known as KDM1A) is the first discovered histone lysine demethylase, with the ability to demethylase H3K4me1/2 and H3K9me1/2 at target loci in a context-dependent manner. LSD1 regulates the balance between self-renewal and differentiation of stem cells, and is highly expressed in various cancers, playing an important role in differentiation and self-renewal of tumor cells. In this review, we summarize recent studies about the LSD1, its role in normal and tumor cells, and the potential use of small molecule LSD1 inhibitors in therapy.
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