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PMID: 15519853 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Renewing the conspiracy theory debate: does Raf function alone to mediate Ras oncogenesis?

Trends in cell biology ·Vol. 14 ·No. 11 ·2004-11-00 ·Pages 639-47

Repasky GA, Chenette EJ, Der CJ

Abstract

Ras proteins function as signal transducers and are mutationally activated in many human cancers. In 1993, Raf was identified as a key downstream effector of Ras signaling, and it was believed then that the primary function of Ras was simply to facilitate Raf activation. However, the subsequent discovery of other proteins that are effectors of Ras function suggested that oncogenic activities of Ras are mediated by both Raf-dependent and Raf-independent signaling. Further complexity arose with the identification of Ras effectors with putative tumor suppressor, rather than oncogenic, functions. However, the recent identification of B-raf mutations in human cancers has renewed the debate regarding whether Raf activation alone promotes Ras-mediated oncogenesis. In this article, we summarize the current knowledge of the contribution of Ras effectors in Ras-mediated oncogenesis.

MeSH Terms
Animals Cell Transformation, Neoplastic Genes, ras Humans Phosphatidylinositol 3-Kinases/metabolism Proto-Oncogene Proteins B-raf/metabolism Signal Transduction
Chemicals
Phosphatidylinositol 3-Kinases Proto-Oncogene Proteins B-raf
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Repasky Gretchen A
The Colorado College, Chemistry Department, Colorado Springs, CO 80903, USA.
Chenette Emily J
Der Channing J
Article Info
Journal
Trends in cell biology
Abbr.
Trends Cell Biol
ISSN
0962-8924
Published
2004-11-00
Pages
639-47
Language
English
Region
England
NLM ID
9200566
Subset
IM
Grants
NCI NIH HHS · CA42978 · United States
NCI NIH HHS · CA63071 · United States
NCI NIH HHS · CA69577 · United States
NIGMS NIH HHS · GM65533 · United States
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