Antimitochondrial agents:: a new class of anticancer agents

被引:7
|
作者
André, N
Rome, A
Carré, M
机构
[1] Hop Enfants La Timone, EA3286, Serv Oncol Pediat, F-13005 Marseille, France
[2] CNRS, FRE, UFR Pharm, F-13005 Marseille, France
来源
ARCHIVES DE PEDIATRIE | 2006年 / 13卷 / 01期
关键词
apoptosis; mitochondria; chemotherapy; neoplasms;
D O I
10.1016/j.arcped.2005.10.003
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Over the last 2 decades, the role of apoptosis in anticancer agent cytotoxicity has become clear. Defects in the regulation of apoptosis (programmed cell death) make important contributions to the pathogenesis and progression of most cancers and leukemias. Apoptosis defects also have a key role in cell resistance to chemotherapy. Mitochondria play a central pail in cell death in response to anticancer agents. Most of these agents target mitochondria via caspases or other regulator elements of the apoptotic machinery. Nevertheless, some anticancer agents, already in clinical use (paclitaxel, vinblastine, lonidamine, etoposide, arsenic trioxide) or in pre-clinical development (betulinic acid, MT21), directly target and permeabilize mitochondria. The acknowledgement of mitochondria as a new target for anticancer agents provides a new way to bypass cancer cell chemoresistance. (c) 2005 Elsevier SAS. Tons droits reserves.
引用
收藏
页码:69 / 75
页数:7
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