Induction of cancer cell apoptosis by α-tocopheryl succinate:: molecular pathways and structural requirements

被引:256
作者
Neuzil, J
Weber, T
Schröder, A
Lu, M
Ostermann, G
Gellert, N
Mayne, GC
Olejnicka, B
Nègre-Salvayre, A
Stícha, M
Coffey, RJ
Weber, C
机构
[1] Univ Munich, Inst Prevent Cardiovasc Dis, D-80336 Munich, Germany
[2] Univ Munich, Med Policlin, D-80336 Munich, Germany
[3] Vanderbilt Univ, Med Ctr N, Nashville, TN USA
[4] Flinders Univ S Australia, Adelaide, SA 5001, Australia
[5] Linkoping Univ Hosp, Dept Pathol 2, Linkoping, Sweden
[6] INSERM, Dept Biochem, Toulouse, France
[7] Charles Univ, Fac Sci, Prague, Czech Republic
关键词
vitamin E succinate; protein kinase C; programmed cell death; colon cancer;
D O I
10.1096/fj.00-0251com
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
The vitamin E analog alpha -tocopheryl succinate (alpha -TOS) can induce apoptosis. We show that the proapoptotic activity of alpha -TOS in hematopoietic and cancer cell lines involves inhibition of protein kinase C (PKC), since phorbol myristyl acetate prevented alpha -TOS-triggered apoptosis. More selective effecters indicated that alpha -TOS reduced PKC alpha isotype activity by increasing protein phosphatase 2A (PP2A) activity. The role of PKC alpha inhibition in alpha -TOS-induced apoptosis was confirmed using antisense oligonucleotides or PKC alpha overexpression. Gain- or loss-of-function bcl-2 mutants implied modulation of bcl-2 activity by PKC/PP2A as a mitochondrial target of alpha -TOS-induced proapoptotic signals. Structural analogs revealed that alpha -tocopheryl and succinyl moieties are both required for maximizing these effects. In mice with colon cancer xenografts, alpha -TOS suppressed tumor growth by 80%. This epitomizes cancer cell killing by a pharmacologically relevant compound without known side effects.
引用
收藏
页码:403 / 415
页数:13
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