Donate Help Contact The AHA Sign In Home
American Heart Association
Arteriosclerosis, Thrombosis, and Vascular Biology
Search: search_blue_button Advanced Search
Published Online
on July 24, 2008

Arteriosclerosis, Thrombosis, and Vascular Biology. 2008
Published online before print July 24, 2008, doi: 10.1161/ATVBAHA.108.172015
A more recent version of this article appeared on October 1, 2008
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
28/10/1703    most recent
ATVBAHA.108.172015v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Silva, R.
Right arrow Articles by Reynolds, L. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Silva, R.
Right arrow Articles by Reynolds, L. E.

Submitted on January 30, 2008
Accepted on July 14, 2008

Integrins. The Keys to Unlocking Angiogenesis

Rita Silva ; Gabriela D'Amico ; Kairbaan M. Hodivala-Dilke ; and Louise E. Reynolds *

From the Adhesion and Angiogenesis Group, Centre for Tumour Biology, Cancer Research UK Clinical Centre and the Institute of Cancer, Barts & The London & Queen Mary's School of Medicine & Dentistry, John Vane Science Centre, Charterhouse Square, London UK.

* To whom correspondence should be addressed. E-mail: louise.reynolds{at}cancer.org.uk.

Abstract—Angiogenesis, the formation of new blood vessels from preexisting vasculature, contributes to the pathogenesis of many disorders, including ischemic diseases and cancer. Integrins are cell adhesion molecules that are expressed on the surface of endothelial cells and pericytes, making them potential targets for antiangiogenic therapy. Here we review the contribution of endothelial and mural cell integrins to angiogenesis and highlight their potential as antiangiogenesis targets.




This article has been cited by other articles:


Home page
J. Cell Sci.Home page
K. Mitchell, C. Szekeres, V. Milano, K. B. Svenson, M. Nilsen-Hamilton, J. A. Kreidberg, and C. M. DiPersio
{alpha}3{beta}1 integrin in epidermis promotes wound angiogenesis and keratinocyte-to-endothelial-cell crosstalk through the induction of MRP3
J. Cell Sci., June 1, 2009; 122(11): 1778 - 1787.
[Abstract] [Full Text] [PDF]