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• W2092775378 abstract "Junctional Adhesion Molecule A (JAM-A) is a member of the Ig superfamily of membrane proteins expressed in platelets, leukocytes, endothelial cells and epithelial cells. We have previously shown that in endothelial cells, JAM-A regulates basic fibroblast growth factor, (FGF-2)-induced angiogenesis via augmenting endothelial cell migration. Recently, we have revealed that in breast cancer cells, down-regulation of JAM-A enhances cancer cell migration and invasion. Further, ectopic expression of JAM-A in highly metastatic MDA-MB-231 cells attenuates cell migration, and down-regulation of JAM-A in low-metastatic T47D cells enhance migration. Interestingly, JAM-A expression is greatly diminished as breast cancer disease progresses. The molecular mechanism of this function of JAM-A is beyond its well-characterized barrier function at the tight junction. Our results point out that JAM-A differentially regulates migration of endothelial and cancer cells." @default.
• W2092775378 created "2016-06-24" @default.
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• W2092775378 date "2008-10-01" @default.
• W2092775378 modified "2023-10-18" @default.
• W2092775378 title "Putting the brakes on cancer cell migration" @default.
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• W2092775378 doi "https://doi.org/10.4161/cam.2.4.6753" @default.
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