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

被引:0
|
作者
Waseem Ahmad Siddiqui
Amjid Ahad
Haseeb Ahsan
机构
[1] Jamia Hamdard (Hamdard University),Department of Biochemistry, Faculty of Science
[2] Jamia Millia Islamia,Department of Biochemistry, Faculty of Dentistry
来源
Archives of Toxicology | 2015年 / 89卷
关键词
Bcl-2; Apoptosis; BH3; Mitochondria; Cancer; Neurodegenerative disorders; Extrinsic pathway;
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学科分类号
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.
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页码:289 / 317
页数:28
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