Zerbini Luiz F, Wang Yihong, Czibere Akos, Correa Ricardo G, Cho Je-Yoel, Ijiri Kosei, Wei Wanjang, Joseph Marie, Gu Xuesong, Grall Franck, Goldring Mary B, Zhou Jin-Rong, Libermann Towia A
Beth Israel Deaconess Medical Center Genomics Center and New England Baptist Bone and Joint Institute, 4 Blackfan Circle, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2004 Sep 14;101(37):13618-23. doi: 10.1073/pnas.0402069101. Epub 2004 Sep 7.
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.
核因子κB/抑制蛋白κB信号通路是癌症中细胞存活的关键调节因子。在此,我们报告核因子κB对生长停滞和DNA损伤诱导蛋白(GADD)45α和γ表达的联合下调是多种癌症类型逃避程序性细胞死亡的关键步骤。我们证明,抑制癌细胞中的核因子κB会导致GADD45α和γ依赖性的细胞凋亡诱导及肿瘤生长抑制。通过小干扰RNA抑制癌细胞中的GADD45α和γ可消除核因子κB抑制剂诱导的细胞凋亡,并阻断c-Jun氨基末端激酶的激活,而GADD45α和γ的过表达则激活c-Jun氨基末端激酶并诱导细胞凋亡。这些结果明确了GADD45家族作为癌细胞中细胞存活的重要介质的作用,对癌症化疗和新型药物研发具有重要意义。