Curcumin induces apoptosis in human breast cancer cells through p53-dependent Bax induction

被引:352
作者
Choudhuri, T
Pal, S
Agwarwal, ML
Das, T
Sa, G
机构
[1] Bose Inst, Anim Physiol Sect, Kolkata 700054, India
[2] Cleveland Clin Fdn, Learner Res Inst, Dept Biol Mol, Cleveland, OH 44195 USA
关键词
apoptosis; breast cancer; curcumin; p53; Bax; bcl-2;
D O I
10.1016/S0014-5793(02)02292-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The aim of this study as to determine the mechanisms of curcumin-induced human breast cancer cell apoptosis. From quantitative image analysis data showing an increase in the percentage of cells with a sub-G0/G1 DNA content, Ne demonstrated curcumin-induced apoptosis in the breast cancer cell line MCF-7, in which expression of wild-type p53 could be induced. Apoptosis was accompanied by an increase in p53 level as well as its DNA-binding activity followed by Bax expression at the protein level. Further experiments using p53-null MDAH041 cell as sell as lose and high p53-expressing TR9-7 cell. in which p53 expression is under tight control of tetracycline. established that curcumin induced apoptosis in tumor cells via a p53-dependent pathway in which Bax is the downstream effector of p53. This property of curcumin suggests that this molecule could haw a possible therapeutic potential in breast cancer patients. (C) 2002 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:334 / 340
页数:7
相关论文
共 33 条
[1]
Curcumin inhibition of inflammatory cytokine production by human peripheral blood monocytes and alveolar macrophages [J].
Abe, Y ;
Hashimoto, S ;
Horie, T .
PHARMACOLOGICAL RESEARCH, 1999, 39 (01) :41-47
[2]
The p53 network [J].
Agarwal, ML ;
Taylor, WR ;
Chernov, MV ;
Chernova, OB ;
Stark, GR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (01) :1-4
[3]
P53 CONTROLS BOTH THE G(2)/M AND THE G(1) CELL-CYCLE CHECKPOINTS AND MEDIATES REVERSIBLE GROWTH ARREST IN HUMAN FIBROBLASTS [J].
AGARWAL, ML ;
AGARWAL, A ;
TAYLOR, WR ;
STARK, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (18) :8493-8497
[4]
PHARMACOLOGY OF CURCUMA-LONGA [J].
AMMON, HPT ;
WAHL, MA .
PLANTA MEDICA, 1991, 57 (01) :1-7
[5]
Curcumin mediated apoptosis in AK-5 tumor cells involves the production of reactive oxygen intermediates [J].
Bhaumik, S ;
Anjum, R ;
Rangaraj, N ;
Pardhasaradhi, BVV ;
Khar, A .
FEBS LETTERS, 1999, 456 (02) :311-314
[6]
T cells from bax alpha transgenic mice show accelerated apoptosis in response to stimuli but do not show restored DNA damage-induced cell death in the absence of p53 [J].
Brady, HJM ;
Salomons, GS ;
Bobeldijk, RC ;
Berns, AJM .
EMBO JOURNAL, 1996, 15 (06) :1221-1230
[7]
Curcumin induces apoptosis in human melanoma cells through a Fas receptor/caspase-8 pathway independent of p53 [J].
Bush, JA ;
Cheung, KJJ ;
Li, G .
EXPERIMENTAL CELL RESEARCH, 2001, 271 (02) :305-314
[8]
COHEN JJ, 1993, IMMUNOL TODAY, V14, P126, DOI 10.1016/0167-5699(93)90214-6
[9]
Induction of cell proliferation and apoptosis: Dependence on the dose of the inducer [J].
Das, T ;
Sa, G ;
Sinha, P ;
Ray, PK .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 260 (01) :105-110
[10]
Mechanisms of protein A superantigen-induced signal transduction for proliferation of mouse B cell [J].
Das, T ;
Sa, G ;
Ray, PK .
IMMUNOLOGY LETTERS, 1999, 70 (01) :43-51