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  • Open Access

G protein signaling in tumor cell growth and metastasis

Molecular Cytogenetics20147 (Suppl 1) :I56

https://doi.org/10.1186/1755-8166-7-S1-I56

  • Published:

Keywords

  • Ovarian Cancer
  • Pancreatic Cancer
  • Ovarian Cancer Cell
  • Protein Signaling
  • Pancreatic Cancer Cell

G protein signaling has been implicated in different aspects cancer growth and progression. Our studies have identified that the G12-family of G proteins that defines the gep family of oncogenes are critically involved in tumor cell proliferation and metastasis. Defining these pathways has shown that the gep protooncogene GNA12 is specifically involved in the proliferation of ovarian cancer cells whereas GNA13 is involved in cancer cell metastasis. Consequently, the silencing of the gep proto-oncogenes potently inhibited tumor growth of ovarian cancer cells in a mouse xenograft model, thus suggesting the dominant role for the gep oncogenes in ovarian cancer growth and progression. In addition we demonstrate a similar role for GNA13 in the invasive migration of pancreatic cancer cells. Furthermore, we demonstrate that an eleven amino acid peptide derived from the gep oncogenes Gα12/13 can effectively disrupt LPA-stimulated oncogenic pathways. Thus, in addition to unraveling the molecular mechanism underlying cancer progression and metastasis, our results provide evidence that the G protein signaling nodes can be targeted for cancer chemotherapy.

This work was supported by grants from the National Institutes of Health (CA123233, CA 125752, CA 116984).

Authors’ Affiliations

(1)
Peggy and Stephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE 10th Street, BRC 1417, Oklahoma City, OK 73012, USA

Copyright

© Dhanasekaran; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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