EZH2型
甲基化
核受体
甲基转移酶
化学
组蛋白
癌症研究
小分子
计算生物学
赖氨酸
组蛋白甲基转移酶
生物
生物化学
氨基酸
转录因子
基因
作者
Aarajana Shrestha,Nayeon Kim,Su‐Jeong Lee,Yong Hyun Jeon,Ji‐Joon Song,Hongchan An,Sung Jin Cho,Tara Man Kadayat,Jungwook Chin
标识
DOI:10.1021/acs.jmedchem.1c01116
摘要
Nuclear receptor-binding SET domain (NSD) proteins are a class of histone lysine methyltransferases (HKMTases) that are amplified, mutated, translocated, or overexpressed in various types of cancers. Several campaigns to develop NSD inhibitors for cancer treatment have begun following recent advances in knowledge of NSD1, NSD2, and NSD3 structures and functions as well as the U.S. FDA approval of the first HKMTase inhibitor (tazemetostat, an EZH2 inhibitor) to treat follicular lymphoma and epithelioid sarcoma. This perspective highlights recent findings on the structures of catalytic su(var), enhancer-of-zeste, trithorax (SET) domains and other functional domains of NSD methyltransferases. In addition, recent progress and efforts to discover NSD-specific small molecule inhibitors against cancer-targeting catalytic SET domains, plant homeodomains, and proline-tryptophan-tryptophan-proline domains are summarized.
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