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Cancer Lett. 2006 Oct 8;242(1):11-9. Epub 2006 Jan 31.

Integrin-mediated cell-matrix interactions for prosurvival and antiapoptotic signaling after genotoxic injury.

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1
OncoRay-Radiation Research in Oncology, Medical Faculty Carl Gustav Carus, University of Technology Dresden,Fetscherstrasse 74/PF 86, 01307 Dresden, Germany. nils.cordes@oncoray.de

Abstract

Interactions of cells with their microenvironment modify the cellular sensitivity of normal and tumor cells for radiation- and drug-induced genotoxic injury. The preexistent or acquired cellular resistance against such agents aggravates anticancer therapies and, therefore, complicates the recovery of patients. Recently, integrin-mediated adhesion was shown to improve cell survival of both normal and cancer cells following DNA damage. Here, I will discuss the role of integrins and integrin-mediated signaling cascades in the survival or death response upon genotoxic stress. Detailed knowledge of the responsible molecular processes might provide implications for putative therapies targeting integrins or integrin-associated molecules to achieve an optimization of anticancer treatments.

PMID:
16448744
DOI:
10.1016/j.canlet.2005.12.004
[Indexed for MEDLINE]
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