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Rho在致癌性Ras诱导的细胞转化中的关键作用。

Critical role of Rho in cell transformation by oncogenic Ras.

作者信息

Prendergast G C, Khosravi-Far R, Solski P A, Kurzawa H, Lebowitz P F, Der C J

机构信息

Wistar Institute, Philadelphia, Pennsylvania 19104, USA.

出版信息

Oncogene. 1995 Jun 15;10(12):2289-96.

PMID:7784077
Abstract

We demonstrate that Rho, a regulator of cytoskeletal actin, is necessary for Ras transformation. A dominant inhibitory Rho gene (RhoBN19) specifically suppressed Rat1 cell focus formation induced by oncogenic Ras but not by Raf. An activated Rho gene (RhoBV14) lacked focus formation activity but augmented the focus formation activity of both oncogenes. NIH3T3 cell lines expressing RhoBV14 grew to higher saturation density and displayed reduced serum and anchorage requirements for growth. We concluded that Rho played a role in cell growth regulation and was required for transformation by oncogenic Ras but not Raf. A model for Ras signal transduction proposing separate Rho-dependent and Raf-dependent pathways is discussed.

摘要

我们证明,细胞骨架肌动蛋白的调节因子Rho是Ras转化所必需的。一个显性抑制性Rho基因(RhoBN19)特异性地抑制了致癌性Ras诱导的Rat1细胞集落形成,但不抑制Raf诱导的集落形成。一个激活的Rho基因(RhoBV14)缺乏集落形成活性,但增强了两种致癌基因的集落形成活性。表达RhoBV14的NIH3T3细胞系生长到更高的饱和密度,并显示出对生长的血清和贴壁需求降低。我们得出结论,Rho在细胞生长调节中起作用,是致癌性Ras而非Raf转化所必需的。本文讨论了一个提出Rho依赖性和Raf依赖性独立信号转导途径的Ras信号转导模型。

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