A Small-Molecule Inhibitor of BCL6 Kills DLBCL Cells In Vitro and In Vivo

被引:236
|
作者
Cerchietti, Leandro C. [2 ,5 ]
Ghetu, Alexandru F. [3 ,4 ]
Zhu, Xiao [1 ]
Da Silva, Gustavo F. [6 ]
Zhong, Shijun [1 ]
Matthews, Marilyn [1 ]
Bunting, Karen L. [2 ,5 ]
Polo, Jose M. [6 ]
Fares, Christophe [3 ,4 ]
Arrowsmith, Cheryl H. [3 ,4 ,7 ]
Yang, Shao Ning [2 ,5 ]
Garcia, Monica [2 ,5 ]
Coop, Andrew [1 ]
MacKerell, Alexander D., Jr. [1 ]
Prive, Gilbert G. [3 ,4 ,7 ,8 ]
Melnick, Ari [2 ,5 ]
机构
[1] Univ Maryland, Sch Pharm, Dept Pharmaceut Sci, Baltimore, MD 21201 USA
[2] Cornell Univ, Weill Cornell Med Coll, Dept Pharmacol, New York, NY 10065 USA
[3] Ontario Canc Inst, Toronto, ON M5G 1L7, Canada
[4] Campbell Family Inst Canc Res, Toronto, ON M5G 1L7, Canada
[5] Cornell Univ, Weill Cornell Med Coll, Div Hematol & Med Oncol, Dept Med, New York, NY 10065 USA
[6] Albert Einstein Coll Med, Dept Dev & Mol Biol, Bronx, NY 10461 USA
[7] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2N9, Canada
[8] Univ Toronto, Dept Biochem, Toronto, ON M5S 1A8, Canada
关键词
GERMINAL-CENTER FORMATION; BTB DOMAIN; EXPRESSION; PHARMACOKINETICS; IDENTIFICATION; DOCKING; COREPRESSOR; MODEL; AZITHROMYCIN; PATHOGENESIS;
D O I
10.1016/j.ccr.2009.12.050
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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 BIB 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.
引用
收藏
页码:400 / 411
页数:12
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