SummaryImpairment of apoptosis, the physiologic cell death process, is central to cancer development and renders tumors refractory to cytotoxic therapy. Bcl-2, the oncoprotein activated in follicular lymphoma, inhibits the conserved cell death pathway triggered by diverse cytotoxic agents, as do several close relatives. A small-molecule antagonist of these proteins has now been designed by Oltersdorf et al. Strikingly, ABT-737 sensitizes many tumors to cytotoxic agents and is effective as a single agent against certain lymphomas and solid tumors, provoking stable regression in some tumor xenografts. Hence, this work validates Bcl-2-like proteins as important new targets in cancer therapy
Defects in apoptotic cell death can promote cancer and impair responses of malignant cells to anti-c...
SummaryCancer cells exhibit many abnormal phenotypes that induce apoptotic signaling via the intrins...
The discovery of the link between defective apoptotic regulation and cancer cell survival engendered...
SummarySince apoptosis is impaired in malignant cells overexpressing prosurvival Bcl-2 proteins, dru...
In this issue of Cancer Cell, two groups present data on the function of an antagonist of BCL-2, ABT...
Intrinsic apoptosis is controlled by the BCL-2 family of proteins but the complexity of intra-family...
Cancer is a heterogeneous group of diseases defined by distinct capabilities, including resistance t...
Apoptosis (or programmed cell death) is a genetically controlled “cell suicide” pathway which plays ...
Several cancer cell types, including chronic lymphocytic leukemia (CLL) and diffuse large B-cell lym...
The ability of a cell to undergo mitochondrial apoptosis is governed by pro- and anti-apoptotic memb...
The failure of apoptosis (programmed cell death) underpins the development of many tumors and often ...
International audienceThe imbalance between BCL-2 homologues and pro-death counterparts frequently n...
AbstractResistance to apoptosis, often achieved by the overexpression of antiapoptotic proteins, is ...
Despite tremendous advances over the last 15 years in understanding fundamental mechanisms of apopto...
Resistance to apoptosis, often achieved by the overexpression of antiapoptotic proteins, is common a...
Defects in apoptotic cell death can promote cancer and impair responses of malignant cells to anti-c...
SummaryCancer cells exhibit many abnormal phenotypes that induce apoptotic signaling via the intrins...
The discovery of the link between defective apoptotic regulation and cancer cell survival engendered...
SummarySince apoptosis is impaired in malignant cells overexpressing prosurvival Bcl-2 proteins, dru...
In this issue of Cancer Cell, two groups present data on the function of an antagonist of BCL-2, ABT...
Intrinsic apoptosis is controlled by the BCL-2 family of proteins but the complexity of intra-family...
Cancer is a heterogeneous group of diseases defined by distinct capabilities, including resistance t...
Apoptosis (or programmed cell death) is a genetically controlled “cell suicide” pathway which plays ...
Several cancer cell types, including chronic lymphocytic leukemia (CLL) and diffuse large B-cell lym...
The ability of a cell to undergo mitochondrial apoptosis is governed by pro- and anti-apoptotic memb...
The failure of apoptosis (programmed cell death) underpins the development of many tumors and often ...
International audienceThe imbalance between BCL-2 homologues and pro-death counterparts frequently n...
AbstractResistance to apoptosis, often achieved by the overexpression of antiapoptotic proteins, is ...
Despite tremendous advances over the last 15 years in understanding fundamental mechanisms of apopto...
Resistance to apoptosis, often achieved by the overexpression of antiapoptotic proteins, is common a...
Defects in apoptotic cell death can promote cancer and impair responses of malignant cells to anti-c...
SummaryCancer cells exhibit many abnormal phenotypes that induce apoptotic signaling via the intrins...
The discovery of the link between defective apoptotic regulation and cancer cell survival engendered...