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© 2005 Oxford University Press
CORRESPONDENCE |
Re: Integrin
3 Leu33Pro Homozygosity and Risk of Cancer
Affiliations of authors: Molecular Biology Laboratory, Department of Obstetrics & Gynecology, University of Ulm, Prittwitzstrasse 43, D-89075 Ulm, Germany (SWG); Division of Clinical Epidemiology, Deutsches Krebsforschungszentrum, Postfach 101949, 69009 Heidelberg, Germany (JCC)
Correspondence to: For correspondence regarding molecular biology: Shan Wang-Gohrke, MD, Department of Obstetrics and Gynecology, University of Ulm, Prittwitzstrasse 43, D-89075 Ulm, Germany (e-mail: shan.wang@medizin.uni-ulm.de); for correspondence regarding epidemiology: Jenny Chang-Claude, PhD, Division of Clinical Epidemiology, Deutsches Krebsforschungszentrum, Postfach 101949, 69009 Heidelberg, Germany (e-mail: J.Chang-Claude@dkfz.de).
| The first 10% of the full text of this article appears below. |
Integrins are transmembrane 
heterodimers that function as key surface adhesion and cell signaling receptors influencing cell proliferation and migration. Overexpression of integrin
3 is associated with progression to invasive tumors, whereas inhibition of
3 integrin expression and/or function is associated with a reduction in tumor growth and metastasis. Specific
3 integrin inhibitors are being developed as cancer drugs, some of which are already in clinical trials.
A functional polymorphism
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3 Leu33Pro Homozygosity and Risk of Cancer
J Natl Cancer Inst 2004 96: 234-235.
3 Leu33Pro Homozygosity and Risk of Cancer
J Natl Cancer Inst 2005 97: 779-780.
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