Chlorimipramine: A novel anticancer agent with a mitochondrial target

被引:68
作者
Daley, E
Wilkie, D
Loesch, A
Hargreaves, IP
Kendall, DA
Pilkington, GJ
Bates, TE [5 ]
机构
[1] Kings Coll London, Inst Psychiat, Dept Neuropathol, Expt Neurooncol Grp, London SE5 8AF, England
[2] UCL, Dept Biol, London WC1E 6BT, England
[3] UCL, Dept Anat & Dev Biol, London WC1E 6BT, England
[4] Natl Hosp Neurol & Neurosurg, Neurometabol Unit, London WC1N 3BG, England
[5] Univ Nottingham, Sch Biomed Sci, MRC, Appl Neurosci Grp,Sch Med,Queens Med Ctr, Nottingham NG7 2UH, England
[6] Inst Neurol, Dept Neurochem, London WC1N BG, England
关键词
cancer; mitochondria; apoptosis; glioma; antidepressant; chlorimipramine; clomipramine;
D O I
10.1016/j.bbrc.2005.01.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondria have been suggested to be a potential intracellular target for cancer chemotherapy. In this report, we demonstrate the ability of the tricyclic antidepressant chlorimipramine to kill human glioma cells in vitro by a molecular mechanism resulting in an increase in caspase 3 activity following inhibition of glioma oxygen consumption. Studies with isolated rat mitochondria showed that chlorimipramine specifically inhibited mitochondrial complex III activity, which causes decreased mitochondrial membrane potential as well as mitochondrial swelling and vacuolation. The use of chlorimipramine in human as an effective, non-toxic cancer therapeutic having a strong selectivity between cancer cells and normal cells on the basis of their mitochondrial function is discussed. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:623 / 632
页数:10
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