Targeting the mitochondrial apoptotic pathway: a preferred approach in hematologic malignancies?

被引:41
作者
Brinkmann, K. [1 ,2 ]
Kashkar, H. [1 ,2 ]
机构
[1] Cologne Excellence Cluster Cellular Stress Respon, CMMC, Cologne, Germany
[2] Univ Cologne, IMMIH, D-50935 Cologne, Germany
关键词
apoptosis; BH3; mimetics; Bcl-2; targeting; BCL-2 ANTISENSE OLIGONUCLEOTIDE; PAN-BCL-2 FAMILY ANTAGONIST; OBATOCLAX MESYLATE GX15-070; ACUTE MYELOID-LEUKEMIA; NON-HODGKINS-LYMPHOMA; PHASE-II MULTICENTER; BH3-ONLY PROTEIN BIM; MANTLE-CELL LYMPHOMA; MYC-DRIVEN MOUSE; OBLIMERSEN SODIUM;
D O I
10.1038/cddis.2014.61
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Acquired resistance toward apoptosis represents one of the hallmarks of human cancer and a major cause of the inefficacy of most anticancer treatment regimens. Based on its ability to inhibit apoptosis, the B-cell lymphoma/leukemia 2 (Bcl-2) protein family has garnered the most attention as a promising therapeutic target in cancer. Accordingly, efforts have lately been focused on the development of drugs targeting Bcl-2 proteins with considerable therapeutic success, particularly in hematologic malignancies. Here, we review the previous studies and highlight the pivotal role of the Bcl-2 protein family in the homeostasis of hematologic tissue compartment. This knowledge provides more insight into why some cancers are more sensitive to Bcl-2 targeting than others and will foster the clinical evaluation of Bcl-2-targeting strategies in cancer by avoiding severe on-target side effects in the development of healthy tissues.
引用
收藏
页码:e1098 / e1098
页数:11
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