| Literature DB >> 30526462 |
Yijie Sun1,2, Yanyi Sun1, Saichao Yue2, Yaohe Wang1, Fanghui Lu1.
Abstract
Histone deacetylases (HDACs), as epigenetic modifiers, are essential for gene transcriptional activities. The alternation of HDACs expression, mutation and/or inappropriate recruitments has been discovered in a broad range of tumors contributing to the tumorigenesis through a serial of biological pathways. HDACs, therefore, are characterized as promising cancer therapeutic targets, and their inhibitors are under rapid development. Here, we discuss HDAC inhibitors in terms of their functional mechanism establishing the anti-tumor effects and potential clinical applications including the synergistic effects in combinational treatment. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.Entities:
Keywords: Cancer treatment; DNA; Epigenetics; Histone Deacetylase; Inhibitors; RNA.
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Year: 2018 PMID: 30526462 DOI: 10.2174/1568026619666181210152115
Source DB: PubMed Journal: Curr Top Med Chem ISSN: 1568-0266 Impact factor: 3.295