| Literature DB >> 20305688 |
S M Pontier1, L Huck, D E White, J Rayment, V Sanguin-Gendreau, B Hennessy, D Zuo, R St-Arnaud, G B Mills, S Dedhar, C J Marshall, W J Muller.
Abstract
Elevated expression of the integrin-linked kinase (ILK) has been observed in a variety of cancers and has been further correlated with poor clinical outcome. Here, we show that mammary epithelial disruption of ILK results in a profound block in mammary tumor induction. Consistent with these observations, inhibition of ILK function in ErbB2-expressing cells with small molecule inhibitor or RNA interference resulted in profound block in their in vitro invasive properties due to the induction of apoptotic cell death. The rare ILK-deficient tumors that eventually arose overcame this block in tumor induction by an upregulation of ErB3 phosphorylation. These observations provide direct evidence that ILK has a critical role in the initiation phase of ErbB2 tumor induction.Entities:
Mesh:
Substances:
Year: 2010 PMID: 20305688 DOI: 10.1038/onc.2010.86
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867