| Literature DB >> 30582481 |
Le Zhao1,2, Yong-Tao Duan3, Ping Lu1, Zhi-Juan Zhang1, Xiao-Ke Zheng1,2, Jun-Lei Wang4, Wei-Sheng Feng1,2.
Abstract
Epigenetics is defined as the stable and heritable alternations in gene expression without changing the DNA nucleotide sequence. The initiation and progression of cancer result from not only genetic mutation, but also aberrant epigenetic regulation, such as DNA methylation and histones acetylation. Although Genetic alternations cannot be reversed, epigenetic modification is a dynamic and reversible process. Over the past few decades, much progress has been made in the research of epigenetic medications and a variety of drugs have been developed targeting at epigenetic regulatory proteins, which are capable of restoring malignant cancer cells to the normal state. The epigenetic drugs currently approved for cancer treatment mainly target at DNA methylation and histones acetylation. In addition, there are a great many epigenetic drugs in clinical trials for cancer therapy, such as inhibitors of DNA methyltransferases, histone deacetylases, histone methyltransferases, lysine specific demethylases, and BET (bromodomain and extra-terminal domain) family proteins. We will discuss the latest developments of these inhibitors and their applications in cancer therapy. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.Entities:
Keywords: Cancer; DNA methylation; Epigeneticzzm321990readers; Epigenetics drugs; Histone methylation; Histones acetylation; Inhibitors.
Mesh:
Substances:
Year: 2018 PMID: 30582481 DOI: 10.2174/1568026619666181224095449
Source DB: PubMed Journal: Curr Top Med Chem ISSN: 1568-0266 Impact factor: 3.295