Title : Role of TGF-beta1 and MAP kinases in the antiproliferative effect of aspirin in human vascular smooth muscle cells.

Pub. Date : 2010 Mar 22

PMID : 20339548






6 Functional Relationships(s)
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1 Role of TGF-beta1 and MAP kinases in the antiproliferative effect of aspirin in human vascular smooth muscle cells. Aspirin transforming growth factor beta 1 Homo sapiens
2 ASA (2 mM) induced TGF-beta1 secretion; however it was unable to induce Smad activation. Aspirin transforming growth factor beta 1 Homo sapiens
3 ASA increased p38(MAPK) phosphorylation in a TGF-beta1-independent manner. Aspirin transforming growth factor beta 1 Homo sapiens
4 Pre-surgical serum levels of TGF-beta1 in patients who took at antiplatelet doses ASA were assessed by ELISA and remained unchanged. Aspirin transforming growth factor beta 1 Homo sapiens
5 CONCLUSIONS/SIGNIFICANCE: In vitro antiproliferative effects of aspirin (at antiinflammatory concentration) on human VSMC obtained from bypass patients are mediated by TGF-beta1 and p38(MAPK). Aspirin transforming growth factor beta 1 Homo sapiens
6 Pre-surgical serum levels of TGF- beta1 from bypass patients who took aspirin at antiplatelet doses did not change. Aspirin transforming growth factor beta 1 Homo sapiens