Regulation of anti-apoptotic BCL2-proteins by non-canonical interactions: The next step forward or two steps back?

被引:16
作者
Beverly, Levi J. [1 ]
机构
[1] Univ Louisville, Div Hematol & Oncol, Dept Med, James Graham Brown Canc Ctr, Louisville, KY 40202 USA
关键词
BCL2; BH3; Apoptosis; Mitochondria; MOMP; BCL-X-L; CELL-CYCLE PROGRESSION; PROTEIN PHOSPHATASE 2A; BH3 MIMETIC ABT-737; FAMILY-MEMBERS; ANTIAPOPTOTIC ACTIVITY; ENDOPLASMIC-RETICULUM; UBIQUITIN LIGASE; DEATH; MCL-1;
D O I
10.1002/jcb.23335
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
All aspects of cellular biology affect the process of regulated cell death, or apoptosis, and disruption of this process is a causative event in many diseases. Therefore, a comprehensive understanding of all pathways that regulate apoptosis would increase our knowledge of basic cellular functions, as well as the etiologies of many diseases. In turn, we may be able to use this knowledge to better treat patients with diseases, including cancer. Although the basic signaling pathway that regulates apoptosis has been known for over 10 years, we still have much to learn about the upstream signaling components that can directly regulate the core apoptosis machinery. The focus of this review will be to direct attention to non-canonical regulators of the BCL2-family of proteins, especially our void of understanding of such interactions, and the controversy that surrounds some such interactions. J. Cell. Biochem. 113: 312, 2012. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:3 / 12
页数:10
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