Rong Rong, Montalbano JoAnne, Jin Weixin, Zhang Jennifer, Garling Maria, Sheikh M Saeed, Huang Ying
Department of Pharmacology, State University of New York, Upstate Medical University, 750 E Adams Street, Syracuse, NY 13210, USA.
Oncogene. 2005 Jul 14;24(30):4867-72. doi: 10.1038/sj.onc.1208660.
Oncogenic Ras proteins transform cells via multiple downstream signaling cascades that are important for cell proliferation and survival. Gadd153, also known as CHOP, is a growth inhibitory and proapoptotic protein and its expression is upregulated by many agents that induce apoptosis. Here, we report our novel findings that oncogenic Ras downregulates Gadd153 expression at both protein and mRNA levels and that such downregulation occurs, at least in part, via decreases in GADD153 mRNA stability. Gadd153 downregulation is specific to oncogenic Ras since another oncogenic family member R-Ras2/TC21 does not downregulate Gadd153. We further demonstrate that the expression of exogenous Gadd153 interferes with Ras-induced oncogenic transformation, which suggests that downregulation of Gadd153 appears to be an important mechanism by which oncogenic Ras promotes cellular transformation. Thus, oncogenic Ras-mediated cellular transformation also involves downmodulation of important molecules such as Gadd153 that negatively regulate cell growth and survival.
致癌性Ras蛋白通过多个对细胞增殖和存活至关重要的下游信号级联反应来转化细胞。Gadd153,也称为CHOP,是一种生长抑制和促凋亡蛋白,其表达受到许多诱导凋亡的因子的上调。在此,我们报告我们的新发现,即致癌性Ras在蛋白质和mRNA水平上均下调Gadd153的表达,并且这种下调至少部分是通过降低GADD153 mRNA稳定性而发生的。Gadd153的下调是致癌性Ras所特有的,因为另一个致癌家族成员R-Ras2/TC21不会下调Gadd153。我们进一步证明,外源性Gadd153的表达会干扰Ras诱导的致癌转化,这表明Gadd153的下调似乎是致癌性Ras促进细胞转化的重要机制。因此,致癌性Ras介导的细胞转化还涉及对诸如Gadd153等负调控细胞生长和存活的重要分子的下调。