NF-κB-mediated repression of growth arrest- and DNA-damage-inducible proteins 45α and γ is essential for cancer cell survival

被引:132
作者
Zerbini, LF
Wang, YH
Czibere, A
Correa, RG
Cho, JY
Ijiri, K
Wei, WJ
Joseph, M
Gu, XS
Grall, F
Goldring, MB
Zhou, JR
Libermann, TA [1 ]
机构
[1] Beth Israel Deaconess Med Ctr, Genom Ctr, Boston, MA 02115 USA
[2] Beth Israel Deaconess Med Ctr, New England Baptist Bone & Joint Inst, Boston, MA 02115 USA
[3] Beth Israel Deaconess Med Ctr, Dept Surg, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
[5] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
关键词
D O I
10.1073/pnas.0402069101
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
The NF-kappaB/IkappaB signaling pathway is a critical regulator of cell survival in cancer. Here, we report that combined down-regulation of growth arrest- and DNA-damage-inducible proteins (GADD)45alpha and gamma expression by NF-kappaB is an essential step for various cancer types to escape programmed cell death. We demonstrate that inhibition of NF-kappaB in cancer cells results in GADD45alpha- and gamma-dependent induction of apoptosis and inhibition of tumor growth. Inhibition of GADD45alpha and gamma in cancer cells by small interfering RNA abrogates apoptosis induction by the inhibitor of NF-kappaB and blocks c-Jun N-terminal kinase activation, whereas overexpression of GADD45alpha and gamma activates c-Jun N-terminal kinase and induces apoptosis. These results establish an unambiguous role for the GADD45 family as an essential mediator of cell survival in cancer cells with implications for cancer chemotherapy and novel drug discovery.
引用
收藏
页码:13618 / 13623
页数:6
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