posted on 2012-10-02, 00:00authored byQiyuan Zhou, Tianji Chen, Joyce Christina F. Ibe, J Usha Raj, Guofei Zhou
Although von Hippel-Lindau protein (pVHL) is known as a tumor suppressor in kidney and other organs, it remains unclear whether pVHL plays a role in lung cancer development. We investigated the role of pVHL in lung cancer cell proliferation, migration, and colonization using stable A549 cells with knockdown of pVHL. We found that knockdown of pVHL promotes epithelial-mesenchymal transition (EMT) in lung cancer cells. Knockdown of pVHL decreased tumor colonization in a tail-vein injection model and decreased cell proliferation, whereas overexpression of constitutive active HIF increased tumor colonization, suggesting a HIF-independent function of pVHL in lung. Knockdown of pVHL decreased phosphorylation of FAK and expression of integrin, suggesting that pVHL regulates lung cancer development via integrin/FAK signaling pathway.
Funding
The work was supported in part by the University of Illinois at Chicago Faculty Scholarship Support Program (GZ), the University of Illinois Cancer Center Pilot Subsidy Program, and supplemental funding from the UIC Center for Clinical and Translational Science (UL1RR029879). This project started at the laboratory of Dr. Jacob I. Sznajder at the Northwestern University.
History
Publisher Statement
NOTICE: this is the author’s version of a work that was accepted for publication in FEBS Letters. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in FEBS Letters, [Vol 586, Issue 10, 2012, May] DOI:10.1016/j.febslet.2012.04.009