BCL6公司
体内
淋巴瘤
加压器
体外
癌症研究
弥漫性大B细胞淋巴瘤
生物
癌基因
细胞培养
分子生物学
化学
抑制因子
细胞
B细胞
基因
生发中心
细胞周期
生物化学
遗传学
基因表达
免疫学
抗体
作者
Leandro Cerchietti,Alexandru F. Ghetu,Xiaohan Zhu,Gustavo F. Da Silva,Shijun Zhong,Marilyn M. Matthews,Karen Bunting,José M. Polo,Christophe Farès,C.H. Arrowsmith,Shao Ning Yang,Monica Garcia,Andrew Coop,Alexander D. MacKerell,Gilbert G. Privé,Ari Melnick
出处
期刊:Cancer Cell
[Cell Press]
日期:2010-04-01
卷期号:17 (4): 400-411
被引量:259
标识
DOI:10.1016/j.ccr.2009.12.050
摘要
The BCL6 transcriptional repressor is the most frequently involved oncogene in diffuse large B cell lymphoma (DLBCL). We combined computer-aided drug design with functional assays to identify low-molecular-weight compounds that bind to the corepressor binding groove of the BCL6 BTB domain. One such compound disrupted BCL6/corepressor complexes in vitro and in vivo, and was observed by X-ray crystallography and NMR to bind the critical site within the BTB groove. This compound could induce expression of BCL6 target genes and kill BCL6-positive DLBCL cell lines. In xenotransplantation experiments, the compound was nontoxic and potently suppressed DLBCL tumors in vivo. The compound also killed primary DLBCLs from human patients.
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