4.3 Article

RhoE is required for contact inhibition and negatively regulates tumor initiation and progression

Journal

ONCOTARGET
Volume 6, Issue 19, Pages 17479-17490

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.4127

Keywords

contact inhibition; metastasis; RhoE; tumor suppression; p27(Kip1)

Funding

  1. Instituto de Salud Carlos III
  2. MINECO [SAF2013-49176-C2-1-R, SAF2012-32117]
  3. Universidad CEU Cardenal Herrera Santander-Copernicus
  4. Generalitat Valenciana

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RhoE is a small GTPase involved in the regulation of actin cytoskeleton dynamics, cell cycle and apoptosis. The role of RhoE in cancer is currently controversial, with reports of both oncogenic and tumor-suppressive functions for RhoE. Using RhoE-deficient mice, we show here that the absence of RhoE blunts contact-inhibition of growth by inhibiting p27(Kip1) nuclear translocation and cooperates in oncogenic transformation of mouse primary fibroblasts. Heterozygous RhoE(+/gt) mice are more susceptible to chemically induced skin tumors and RhoE knock-down results in increased metastatic potential of cancer cells. These results indicate that RhoE plays a role in suppressing tumor initiation and progression.

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