Measurement of BH3-only protein tolerance

被引:0
作者
Haiming Dai
Husheng Ding
Kevin L Peterson
X Wei Meng
Paula A Schneider
Katherine L B Knorr
Scott H Kaufmann
机构
[1] Anhui Province Key Laboratory of Medical Physics and Technology,Division of Oncology Research, Department of Oncology
[2] Center of Medical Physics and Technology,Department of Molecular Pharmacology and Experimental Therapeutics
[3] Chinese Academy of Sciences,undefined
[4] Hefei,undefined
[5] China,undefined
[6] Cancer Hospital,undefined
[7] Hefei Institutes of Physical Science,undefined
[8] Chinese Academy of Sciences,undefined
[9] Mayo Clinic,undefined
[10] Mayo Clinic,undefined
来源
Cell Death & Differentiation | 2018年 / 25卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
The BCL2 family of proteins regulates cellular life and death decisions. Among BCL2 family members, BH3-only proteins have critical roles by neutralizing antiapoptotic family members, as well as directly activating BAX and BAK. Despite widespread occurrence of BH3-only protein upregulation in response to various stresses, this process is rarely quantified. Moreover, it is unclear whether all BH3-only proteins are equipotent at inducing cell death. Here we show that BH3-only proteins increase as much as 15- to 20-fold after various treatments and define a parameter, termed BH3-only tolerance, which measures how many copies of a particular BH3-only protein can be expressed before the majority of cells in a population undergo apoptosis. We not only assess the relative contributions of anti- and proapoptotic BCL2 family members to BH3-only tolerance, but also illustrate how the study of this parameter can be used to understand cellular sensitivity to anticancer drugs and new combinations. These observations provide a new quantitative framework for assessing apoptotic susceptibility under various conditions.
引用
收藏
页码:282 / 293
页数:11
相关论文
共 285 条
[1]  
Fuchs Y(2011)Programmed cell death in animal development and disease Cell 147 742-758
[2]  
Steller H(2015)An interconnected hierarchical model of cell death regulation by the BCL-2 family Nat Cell Biol 17 1270-1281
[3]  
Chen HC(2002)Apoptosis. A link between cancer genetics and chemotherapy Cell 108 153-164
[4]  
Kanai M(2002)The Bcl2 family: regulators of the cellular life-or-death switch Nat Rev Cancer 2 647-656
[5]  
Inoue-Yamauchi A(2013)Mitochondria: gatekeepers of response to chemotherapy Trends Cell Biol 23 612-619
[6]  
Tu HC(2016)Thirty years of BCL-2: translating cell death discoveries into novel cancer therapies Nat Rev Cancer 16 99-109
[7]  
Huang Y(1988)Bcl-2 gene promotes haemopoietic cell survival and cooperates with c-myc to immortalize pre-B cells Nature 335 440-442
[8]  
Ren D(2010)The landscape of somatic copy-number alteration across human cancers Nature 463 899-905
[9]  
Johnstone RW(2000)Role of BAX in the apoptotic response to anticancer agents Science 290 989-992
[10]  
Ruefli AA(2012)A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer Nat Med 18 521-528