Resveratrol, a tumor-suppressive compound from grapes, induces apoptosis via a novel mitochondrial pathway controlled by Bcl-2

被引:168
作者
Tinhofer, I
Bernhard, D
Senfter, M
Anether, G
Loeffler, M
Kroemer, G
Kofler, R
Csordas, A
Greil, R
机构
[1] Univ Innsbruck, Dept Internal Med, Lab Mol Cytol, A-6020 Innsbruck, Austria
[2] Univ Innsbruck, Tyrolean Canc Res Inst, A-6020 Innsbruck, Austria
[3] Univ Innsbruck, Inst Gen & Expt Pathol, A-6020 Innsbruck, Austria
[4] Inst Gustave Roussy, CNRS, UMR 1599, F-94805 Villejuif, France
[5] Univ Innsbruck, Inst Med Chem & Biochem, A-6020 Innsbruck, Austria
关键词
cell death; antioxidant; cytochrome c-independent; lymphoblastic leukemia;
D O I
10.1096/fj.00-0675fje
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
We report that resveratrol (3,5,4'-trihydroxy-trans-stilbene), a phytoalexin found in grapes and other plant food, induced a breakdown of the mitochondrial transmembrane potential (DeltaPsi(m)) in T-acute lymphoblastic leukemia cells and swelling of isolated rat mitochondria. The breakdown of DeltaPsi(m) was accompanied by the production of reactive oxygen species (ROS), and preceded phosphatidylserine exposure and DNA fragmentation. Breakdown of DeltaPsi(m) was not caused by the activation of caspase-8 or Bid, as no significant cleavage of these proteins could be detected in the induction phase of resveratrol-induced apoptosis. Though loss of DeltaPsi(m) was not followed by cytochrome c translocation to the cytosol, the mitochondrial changes triggered significant activation of caspase-9, -2, -3, and -6. Inhibition of DeltaPsi(m) breakdown and of ROS generation by N-acetylcysteine, or by overexpression of Bcl-2 protein, prevented apoptosis induction by resveratrol. The Bcl-2 expression status of tumor cells should therefore be considered relevant for potential clinical application of resveratrol as anticancer agent.
引用
收藏
页码:1613 / +
页数:26
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