The BCL-2 protein family: opposing activities that mediate cell death
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- 1 January 2008
- journal article
- review article
- Published by Springer Nature in Nature Reviews Molecular Cell Biology
- Vol. 9 (1), 47-59
- https://doi.org/10.1038/nrm2308
Abstract
BCL-2 family proteins, which have either pro- or anti-apoptotic activities, have been studied intensively for the past decade owing to their importance in the regulation of apoptosis, tumorigenesis and cellular responses to anti-cancer therapy. They control the point of no return for clonogenic cell survival and thereby affect tumorigenesis and host-pathogen interactions and regulate animal development. Recent structural, phylogenetic and biological analyses, however, suggest the need for some reconsideration of the accepted organizational principles of the family and how the family members interact with one another during programmed cell death. Although these insights into interactions among BCL-2 family proteins reveal how these proteins are regulated, a unifying hypothesis for the mechanisms they use to activate caspases remains elusive.Keywords
This publication has 164 references indexed in Scilit:
- Role of Mitochondrial Remodeling in Programmed Cell Death in Drosophila melanogasterDevelopmental Cell, 2007
- Voltage-dependent anion channels are dispensable for mitochondrial-dependent cell deathNature Cell Biology, 2007
- The Bcl-2 apoptotic switch in cancer development and therapyOncogene, 2007
- Cytosolic factor- and TOM-independent import of C-tail-anchored mitochondrial outer membrane proteinsThe EMBO Journal, 2006
- Regulated targeting of Bax and Bak to intracellular membranes during apoptosisCell Death & Differentiation, 2006
- Bcl-2 changes conformation to inhibit Bax oligomerizationThe EMBO Journal, 2006
- Promoting apoptosis as a strategy for cancer drug discoveryNature Reviews Cancer, 2005
- Biophysical Characterization of the Oligomeric State of Bax and Its Complex Formation with Bcl-XLBiochemical and Biophysical Research Communications, 1999
- Bcl-xL forms an ion channel in synthetic lipid membranesNature, 1997
- Cloning the chromosomal breakpoint of t(14;18) human lymphomas: clustering around Jh on chromosome 14 and near a transcriptional unit on 18Cell, 1985