New dimension in therapeutic targeting of BCL-2 family proteins

被引:89
|
作者
Besbes, Samaher [1 ,2 ]
Mirshahi, Massoud [1 ,2 ]
Pocard, Marc [1 ,2 ]
Billard, Christian [1 ,2 ]
机构
[1] Hop Lariboisiere, INSERM, U 965, F-75475 Paris, France
[2] Univ Paris Diderot, UMR S965, Paris, France
关键词
anticancer therapy; apoptosis; targeting BCL-2 family proteins; BH3; mimetics; prosurvival protein antagonists; SELECTIVE SMALL-MOLECULE; ENDOPLASMIC-RETICULUM STRESS; STRUCTURE-GUIDED DESIGN; PAN-ACTIVE INHIBITOR; MCL-1; INHIBITORS; CELL-DEATH; HIGH-AFFINITY; RATIONAL DESIGN; IN-VIVO; POTENT;
D O I
10.18632/oncotarget.3868
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Proteins of the BCL-2 family control the mitochondrial pathway of apoptosis. Targeting these proteins proves to be an attractive strategy for anticancer therapy. The biological context is based on the fact that BH3-only members of the family are specific antagonists of prosurvival members. This prompted the identification of "BH3 mimetic" compounds. These small peptides or organic molecules indeed mimic the BH3 domain of BH3-only proteins: by selectively binding and antagonizing prosurvival proteins, they can induce apoptosis in malignant cells. Some small-molecule inhibitors of prosurvival proteins have already entered clinical trials in cancer patients and two of them have shown significant therapeutic effects. The latest developments in the field of targeting BCL-2 family proteins highlight several new antagonists of prosurvival proteins as well as direct activators of proapoptotic proteins. These compounds open up novel prospects for the development of BH3 mimetic anticancer drugs.
引用
收藏
页码:12862 / 12871
页数:10
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