BCL6公司
生发中心
加压器
化学
淋巴瘤
癌症研究
体外
B细胞
体内
弥漫性大B细胞淋巴瘤
免疫系统
计算生物学
抑制因子
细胞生物学
转录因子
抗体
生物化学
生物
免疫学
遗传学
基因
作者
Yong Ai,Lucia Hwang,Alexander D. MacKerell,Ari Melnick,Fengtian Xue
标识
DOI:10.1021/acs.jmedchem.0c01686
摘要
B-cell lymphoma 6 (BCL6) is a master regulator of germinal center formation that produce antibody-secreting plasma cells and memory B-cells for sustained immune responses. The BTB domain of BCL6 (BCL6BTB) forms a homodimer that mediates transcriptional repression by recruiting its corepressor proteins to form a biologically functional transcriptional complex. The protein–protein interaction (PPI) between the BCL6BTB and its corepressors has emerged as a therapeutic target for the treatment of DLBCL and a number of other human cancers. This Perspective provides an overview of recent advances in the development of BCL6BTB inhibitors from reversible inhibitors, irreversible inhibitors, to BCL6 degraders. Inhibitor design and medicinal chemistry strategies for the development of novel compounds will be provided. The binding mode of new inhibitors to BCL6BTB are highlighted. Also, the in vitro and in vivo assays used for the evaluation of new compounds will be discussed.
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