Possible involvement of the inactivation of the Rho-Rho-kinase pathway in oncogenic Ras-induced transformation

Ichiro Izawa, Mutsuki Amano, Kazuyasu Chihara, Takaharu Yamamoto, Kozo Kaibuchi

Research output: Contribution to journalArticle

45 Citations (Scopus)

Abstract

Recent evidence has strongly suggested the involvement of Rho family small guanosine triphosphatases (GTPases) in Ras-induced transformation. To further clarify the role of Rho family GTPases in Ras-induced transformation, we examined the effects of dominant active or dominant negative forms of Rho family GTPases on the morphological changes induced by oncogenic Ras (Ras(V12)) in Rat1 fibroblasts. The cells expressing Ras(V12) showed the severe disruption of actin stress fibers and cell adhesions. The coexpression of dominant active form of Rho (Rho(V14)) reverted not only the formation of stress fibers and focal adhesions but also cell-cell adhesions in Ras-transformed Rat1 cells. In addition, the coexpression of constitutively activated Rho-kinase, a downstream effector of Rho, restored the assembly of stress fibers and focal adhesions. Treatment of Rat1 cells with lysophosphatidic acid, which is known to activate the Rho-Rho-kinase pathway, enhanced the stress fiber formation, whereas it failed to induce the stress fiber formation in the cells expressing Ras(V12). These results suggest that the Rho-Rho-kinase pathway may be inactivated in the cells expressing Ras(V12), and this may contribute to oncogenic Ras-induced transformation.

Original languageEnglish
Pages (from-to)2863-2871
Number of pages9
JournalOncogene
Volume17
Issue number22
DOIs
Publication statusPublished - 03-12-1998
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Genetics
  • Cancer Research

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