TIMP-2 upregulates RECK expression via dephosphorylation of paxillin tyrosine residues 31 and 118

We previously demonstrated that TIMP-2 increases the association of Crk with C3G and via subsequent activation of Rap1 enhances the expression of RECK, a membrane-anchored MMP inhibitor. In the present study, we investigate the mechanism of how the TIMP-2 signal is transduced from the α3β1 integrin...

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Hlavní autoři: Oh, Junseo, Diaz, Terre, Wei, Beiyang, Chang, Hyeujin, Noda, Makoto, Stetler-Stevenson, William G.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2006
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1502148/
https://ncbi.nlm.nih.gov/pubmed/16491114
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.onc.1209444
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