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PMID: 9622053 Published · ppublish English Journal Article Review

Role of Crk oncogene product in physiologic signaling.

Critical reviews in oncogenesis ·Vol. 8 ·No. 4 ·1997-00-00 ·Pages 329-42

Kiyokawa E, Mochizuki N, Kurata T, Matsuda M

Abstract

v-Crk is a member of the family of adaptor-type signaling molecules that consist mostly of SH2 and SH3 domains. The cellular homologs of v-Crk includes CrkI, CrkII, and CrkL; these have been isolated from species ranging from lower vertebrates to man. Crk-family proteins are involved in a variety of signaling cascades such as those of growth factor receptor, integrin, T-cell receptor, B-cell antigen receptor, and cytokines. It has been postulated that the primary function of Crk is to recruit cytoplasmic proteins in the vicinity of tyrosine kinases through SH2-phosphotyrosine interaction. Thus, the output from Crk depends on the SH3-binding proteins, which include the C3G guanine nucleotide exchange protein for Rap1, Abl tyrosine kinase, DOCK180, and the Sos guanine nucleotide exchange protein for Ras. The variety of the Crk-binding proteins indicate the pleiotropic function of Crk.

MeSH Terms
Animals ErbB Receptors/metabolism Humans Integrins/physiology Models, Chemical Oncogene Protein v-crk Oncogenes Protein-Tyrosine Kinases/metabolism Receptors, Cell Surface/physiology Retroviridae Proteins, Oncogenic/physiology Signal Transduction Vertebrates src Homology Domains
Chemicals
Integrins Oncogene Protein v-crk Receptors, Cell Surface Retroviridae Proteins, Oncogenic ErbB Receptors Protein-Tyrosine Kinases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kiyokawa E
Department of Pathology, National Institute of Infectious Diseases, International Medical Center of Japan, Tokyo.
Mochizuki N
Kurata T
Matsuda M
Article Info
Journal
Critical reviews in oncogenesis
Abbr.
Crit Rev Oncog
ISSN
0893-9675
Published
1997-00-00
Pages
329-42
Language
English
Region
United States
NLM ID
8914610
Subset
IM
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