| Literature DB >> 19782465 |
Min Kyung Baek1, Jung Sun Park, Ji Hye Park, Mi Ha Kim, Ho Dong Kim, Woo Kyun Bae, Ik Joo Chung, Boo Ahn Shin, Young Do Jung.
Abstract
The secondary bile acid lithocholic acid (LCA) induced expression of urokinase-type plasminogen activator receptor (uPAR) and enhanced cell invasiveness in colon cancer cells. A dominant negative mutant or a specific inhibitor of MEK-1 suppressed LCA-induced uPAR expression. Deletions and site-directed mutagenesis revealed that the AP-1 site was required for LCA-induced uPAR transcription. LCA-mediated enhanced cell invasiveness was partially abrogated by uPAR neutralizing antibody and inhibitors of both Erk-1/2 and AP-1. These results suggest that LCA induces uPAR expression via Erk-1/2 and AP-1 pathway and, in turn, stimulate invasiveness of human colon cancer cells. 2009 Elsevier Ireland Ltd. All rights reserved.Entities:
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Year: 2009 PMID: 19782465 DOI: 10.1016/j.canlet.2009.08.030
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679