Role of BAX in the apoptotic response to anticancer agents

被引:776
作者
Zhang, L
Yu, J
Park, BH
Kinzler, KW
Vogelstein, B [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Ctr Oncol, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Sch Med, Program Human Genet, Baltimore, MD 21231 USA
关键词
D O I
10.1126/science.290.5493.989
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To assess the role of BAX in drug-induced apoptosis in human colorectal cancer cells, we generated cells that Lack functional BAX genes. Such cells were partially resistant to the apoptotic effects of the chemotherapeutic agent 5-fluorouracil, but apoptosis was not abolished. In contrast, the absence of BAX completely abolished the apoptotic response to the chemopreventive agent sulindac and other nonsteroidal anti-inflammatory drugs (NSAIDs). NSAIDs inhibited the expression of the antiapoptotic protein Bcl-X-L, resulting in an altered ratio of BAX to BcL-X-L and subsequent mitochondria-mediated cell death. These results establish an unambiguous role for BAX in apoptotic processes in human epithelial cancers and may have implications for cancer chemoprevention strategies.
引用
收藏
页码:989 / +
页数:5
相关论文
共 23 条
[1]   Disruption of p53 in human cancer cells alters the responses to therapeutic agents [J].
Bunz, F ;
Hwang, PM ;
Torrance, C ;
Waldman, T ;
Zhang, YG ;
Dillehay, L ;
Williams, J ;
Lengauer, C ;
Kinzler, KW ;
Vogelstein, B .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (03) :263-269
[2]   Requirement for p53 and p21 to sustain G2 arrest after DNA damage [J].
Bunz, F ;
Dutriaux, A ;
Lengauer, C ;
Waldman, T ;
Zhou, S ;
Brown, JP ;
Sedivy, JM ;
Kinzler, KW ;
Vogelstein, B .
SCIENCE, 1998, 282 (5393) :1497-1501
[3]   gamma-ray-induced apoptosis in transgenic mice with proliferative abnormalities in their intestinal epithelium: Re-entry of villus enterocytes into the cell cycle does not affect their radioresistance but enhances the radiosensitivity of the crypt by inducing p53 [J].
Coopersmith, CM ;
Gordon, JI .
ONCOGENE, 1997, 15 (02) :131-141
[4]   Mitochondria and apoptosis [J].
Green, DR ;
Reed, JC .
SCIENCE, 1998, 281 (5381) :1309-1312
[5]   BCL-2 family members and the mitochondria in apoptosis [J].
Gross, A ;
McDonnell, JM ;
Korsmeyer, SJ .
GENES & DEVELOPMENT, 1999, 13 (15) :1899-1911
[6]   Enforced dimerization of BAX results in its translocation, mitochondrial dysfunction and apoptosis [J].
Gross, A ;
Jockel, J ;
Wei, MC ;
Korsmeyer, SJ .
EMBO JOURNAL, 1998, 17 (14) :3878-3885
[7]   PPARδ is an APC-regulated target of nonsteroidal anti-inflammatory drugs [J].
He, TC ;
Chan, TA ;
Vogelstein, B ;
Kinzler, KW .
CELL, 1999, 99 (03) :335-345
[8]   Changes in p21WAF1, pRb, Mdm-2, Bax and Bcl-2 expression in cervical cancer cell lines transfected with a p53 expressing adenovirus [J].
Huang, TG ;
Ip, SM ;
Yeung, WSB ;
Ngan, HYS .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (02) :249-256
[9]   Mutational inactivation of the proapoptotic gene BAX confers selective advantage during tumor clonal evolution [J].
Ionov, Y ;
Yamamoto, H ;
Krajewski, S ;
Reed, JC ;
Perucho, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (20) :10872-10877
[10]   UBIQUITOUS SOMATIC MUTATIONS IN SIMPLE REPEATED SEQUENCES REVEAL A NEW MECHANISM FOR COLONIC CARCINOGENESIS [J].
IONOV, Y ;
PEINADO, MA ;
MALKHOSYAN, S ;
SHIBATA, D ;
PERUCHO, M .
NATURE, 1993, 363 (6429) :558-561