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PMID: 15805241 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. Review

Emerging role of RAB GTPases in cancer and human disease.

Cancer research ·Vol. 65 ·No. 7 ·2005-04-01 ·Pages 2516-9

Cheng KW, Lahad JP, Gray JW, Mills GB

Abstract

Emerging evidence implicates alterations in the RAB small GTPases and their associated regulatory proteins and effectors in multiple human diseases including cancer. We have recently shown that RAB25, located at chromosome 1q22, is amplified at the DNA level and overexpressed at the RNA level in ovarian and breast cancer. These changes correlated with a worsened outcome in both diseases. In addition, enforced expression of RAB25 in both breast and ovarian cancer cells decreased apoptosis and increased proliferation and aggressiveness in vivo, potentially explaining the worsened prognosis. A better understanding of genetic alterations as well as the physiologic and pathophysiologic roles of RAB GTPases may open new opportunities for therapeutic intervention and better outcomes.

MeSH Terms
Breast Neoplasms/enzymology,pathology Female Humans Ovarian Neoplasms/enzymology,pathology rab GTP-Binding Proteins/physiology
Chemicals
rab GTP-Binding Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Cheng Kwai W
Department of Molecular Therapeutics, University of Texas M.D. Anderson Cancer Center, Houston, Texas 77054, USA. kwcheng@mdanderson.org
Lahad John P
Gray Joseph W
Mills Gordon B
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
2005-04-01
Pages
2516-9
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NCI NIH HHS · P30 CA16672-28 · United States
NCI NIH HHS · P50-CA58207 · United States
NCI NIH HHS · P50-CA83639 · United States
OAPP OPHS HHS · PPG-P01 CA64602 · United States
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