The mystery of BCL2 family: Bcl-2 proteins and apoptosis: an update

被引:576
作者
Siddiqui, Waseem Ahmad [1 ]
Ahad, Amjid [1 ]
Ahsan, Haseeb [2 ]
机构
[1] Jamia Hamdard, Dept Biochem, Fac Sci, New Delhi 110062, India
[2] Jamia Millia Islamia, Dept Biochem, Fac Dent, New Delhi 110025, India
关键词
Bcl-2; Apoptosis; BH3; Mitochondria; Cancer; Neurodegenerative disorders; Extrinsic pathway; CYTOCHROME-C RELEASE; NF-KAPPA-B; MITOCHONDRIAL-MEMBRANE PERMEABILIZATION; ENDOPLASMIC-RETICULUM STRESS; CHRONIC LYMPHOCYTIC-LEUKEMIA; TUMOR-SUPPRESSOR P53; CELL-DEATH; X-L; BH3-ONLY PROTEINS; BH3; DOMAINS;
D O I
10.1007/s00204-014-1448-7
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Apoptosis is a critically important biological process that plays an essential role in cell fate and homeostasis. An important component of the apoptotic pathway is the family of proteins commonly known as the B cell lymphoma-2 (Bcl-2). The primary role of Bcl-2 family members is the regulation of apoptosis. Although the structure of Bcl-2 family of proteins was reported nearly 10 years ago, however, it still surprises us with its structural and functional complexity and diversity. A number of studies have demonstrated that Bcl-2 family influences many other cellular processes beyond apoptosis which are generally independent of the regulation of apoptosis, suggesting additional roles for Bcl-2. The disruption of the regulation of apoptosis is a causative event in many diseases. Since the Bcl-2 family of proteins is the key regulator of apoptosis, the abnormalities in its function have been implicated in many diseases including cancer, neurodegenerative disorders, ischemia and autoimmune diseases. In the past few years, our understanding of the mechanism of action of Bcl-2 family of proteins and its implications in various pathological conditions has enhanced significantly. The focus of this review is to summarize the current knowledge on the structure and function of Bcl-2 family of proteins in apoptotic cellular processes. A number of drugs have been developed in the past few years that target different Bcl-2 members. The role of Bcl-2 proteins in the pathogenesis of various diseases and their pharmacological significance as effective molecular therapeutic targets is also discussed.
引用
收藏
页码:289 / 317
页数:29
相关论文
共 270 条
[21]  
BOYD JM, 1995, ONCOGENE, V11, P1921
[22]   Appearance of phosphatidylserine on apoptotic cells requires calcium-mediated nonspecific flip-flop and is enhanced by loss of the aminophospholipid translocase [J].
Bratton, DL ;
Fadok, VA ;
Richter, DA ;
Kailey, JM ;
Guthrie, LA ;
Henson, PM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (42) :26159-26165
[23]   Regulation of the Apaf-1-caspase-9 apoptosome [J].
Bratton, Shawn B. ;
Salvesen, Guy S. .
JOURNAL OF CELL SCIENCE, 2010, 123 (19) :3209-3214
[24]   Posttranslational modification of Bcl-2 facilitates its proteasome-dependent degradation: Molecular characterization of the involved signaling pathway [J].
Breitschopf, K ;
Haendeler, J ;
Malchow, P ;
Zeiher, AM ;
Dimmeler, S .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (05) :1886-1896
[25]   The permeability transition pore complex in cancer cell death [J].
Brenner, C. ;
Grimm, S. .
ONCOGENE, 2006, 25 (34) :4744-4756
[26]   Mitochondrial cell death effectors [J].
Brenner, Dirk ;
Mak, Tak W. .
CURRENT OPINION IN CELL BIOLOGY, 2009, 21 (06) :871-877
[27]   The Bax carboxy-terminal hydrophobic helix does not determine organelle-specific targeting but is essential for maintaining Bax in an inactive state and for stable mitochondrial membrane insertion [J].
Brock, Stephanie E. ;
Li, Chi ;
Wattenberg, Binks W. .
APOPTOSIS, 2010, 15 (01) :14-27
[28]   Control of mitochondrial apoptosis by the Bcl-2 family [J].
Brunelle, Joslyn K. ;
Letai, Anthony .
JOURNAL OF CELL SCIENCE, 2009, 122 (04) :437-441
[29]   Akt promotes cell survival by phosphorylating and inhibiting a forkhead transcription factor [J].
Brunet, A ;
Bonni, A ;
Zigmond, MJ ;
Lin, MZ ;
Juo, P ;
Hu, LS ;
Anderson, MJ ;
Arden, KC ;
Blenis, J ;
Greenberg, ME .
CELL, 1999, 96 (06) :857-868
[30]   Regulation of cell death protease caspase-9 by phosphorylation [J].
Cardone, MH ;
Roy, N ;
Stennicke, HR ;
Salvesen, GS ;
Franke, TF ;
Stanbridge, E ;
Frisch, S ;
Reed, JC .
SCIENCE, 1998, 282 (5392) :1318-1321