| Literature DB >> 22340592 |
Tara Karnezis1, Ramin Shayan, Carol Caesar, Sally Roufail, Nicole C Harris, Kathryn Ardipradja, You Fang Zhang, Steven P Williams, Rae H Farnsworth, Ming G Chai, Thusitha W T Rupasinghe, Dedreia L Tull, Megan E Baldwin, Erica K Sloan, Stephen B Fox, Marc G Achen, Steven A Stacker.
Abstract
Lymphatic metastasis is facilitated by lymphangiogenic growth factors VEGF-C and VEGF-D that are secreted by some primary tumors. We identified regulation of PGDH, the key enzyme in prostaglandin catabolism, in endothelial cells of collecting lymphatics, as a key molecular change during VEGF-D-driven tumor spread. The VEGF-D-dependent regulation of the prostaglandin pathway was supported by the finding that collecting lymphatic vessel dilation and subsequent metastasis were affected by nonsteroidal anti-inflammatory drugs (NSAIDs), known inhibitors of prostaglandin synthesis. Our data suggest a control point for cancer metastasis within the collecting lymphatic endothelium, which links VEGF-D/VEGFR-2/VEGFR-3 and the prostaglandin pathways. Collecting lymphatics therefore play an active and important role in metastasis and may provide a therapeutic target to restrict tumor spread. Copyright ÂEntities:
Mesh:
Substances:
Year: 2012 PMID: 22340592 DOI: 10.1016/j.ccr.2011.12.026
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743