乙酰化
癌症表观遗传学
组蛋白脱乙酰基酶
组蛋白脱乙酰酶抑制剂
癌症研究
生物
组蛋白
表观遗传学
伏立诺他
敏化
HDAC10型
组蛋白脱乙酰基酶2
医学
HDAC11型
曲古抑菌素A
化学
药理学
组蛋白脱乙酰基酶5
组蛋白甲基转移酶
生物化学
基因
免疫学
作者
Huanran Sun,Jiaqi Song,Mingming Sun,Changliang Shan
出处
期刊:Elsevier eBooks
[Elsevier]
日期:2021-01-01
卷期号:: 25-39
被引量:1
标识
DOI:10.1016/b978-0-12-823684-0.00014-1
摘要
Epigenetic alterations play a pivotal role in tumor initiation and progression. Histone deacetylases (HDACs) are a family of epigenetic enzymes that affect gene transcription by inducing histone deacetylation, and then regulate fundamental cellular processes including proliferation, differentiation, and development. It is reported that the expression of histone deacetylase (HDAC) is abnormal in multiple cancer. Targeting HDAC to develop inhibitors is an effective way in treating cancer and enhancing sensitization of tumor to chemotherapeutic drugs. In this chapter, we mainly summarize the different classes of histone deacetylase inhibitors (HDACi) and discuss how HDACi combine with chemotherapeutic drugs to enhance their sensitization.
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