Role of the β isoform of 14-3-3 proteins in cellular proliferation and oncogenic transformation

被引:81
作者
Takihara, Y
Matsuda, Y
Hara, J
机构
[1] Osaka Univ, Microbial Dis Res Inst, Dept Med Genet & Mol Cell Biol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Sch Med, Dept Dev Med, Suita, Osaka 5650871, Japan
关键词
D O I
10.1093/carcin/21.11.2073
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The 14-3-3 proteins are associated with proto-oncogene and oncogene products. Here, we generated NIH 3T3 cells overexpressing the beta isoform of the 14-3-3 proteins (14-3-3 beta) to examine the function of this isoform in cellular proliferation and oncogenic transformation. Overexpression of 14-3-3 beta in NIH 3T3 cells stimulated cell growth and supported anchorage-independent growth in soft agar medium and tumor formation in nude mice. To elucidate the molecular mechanisms of 14-3-3 beta -mediated NIH 3T3 transformation, we examined the activity of mitogen-activated protein kinase (MAPK) after serum stimulation. Overexpression of 14-3-3 beta augmented MAPK activity after serum stimulation, and MAPK activity correlated well with the amount of 14-3-3 beta expression. The colony-forming ability of NIH 3T3 cells overexpressing 14-3-3 beta in soft agar medium was efficiently abolished by exogenous expression of a dominant-negative mutant of MEK1 and 14-3-3 beta physically interacted with Raf-1 in these cells. These findings indicate that 14-3-3 beta has oncogenic potential, mainly through enhancement of Raf-1 activation and resultant augmentation of signaling in the MAPK cascade.
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收藏
页码:2073 / 2077
页数:5
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