Resveratrol suppresses pulmonary tumor metastasis by inhibiting platelet-mediated angiogenic responses

Abstract Background To explore the impact of Resveratrol (RSV) on the angiogenic potential of activated platelets and to elucidate the underlying mechanism. Methods Vascular endothelial growth factor concentrations were measured by enzyme-linked immunosorbent assay. Capillary tube formation assay wa...

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Veröffentlicht in:The Journal of surgical research 2017-09, Vol.217, p.113-122
Hauptverfasser: He, Liwei, PhD, Fan, Fangtian, PhD, Hou, Xianbang, MD, Gao, Cuixiang, MD, Meng, Li, MD, Meng, Shu, MD, Huang, Shiwen, PhD, Wu, Hongyan, PhD
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Sprache:eng
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Zusammenfassung:Abstract Background To explore the impact of Resveratrol (RSV) on the angiogenic potential of activated platelets and to elucidate the underlying mechanism. Methods Vascular endothelial growth factor concentrations were measured by enzyme-linked immunosorbent assay. Capillary tube formation assay was used to examine the impact of RSV on the angiogenic potential of activated platelets. The levels of cyclic adenosine monophosphate and cyclic guanosine monophosphate (cGMP) in the supernatant were evaluated using corresponding enzyme-linked immunosorbent assay kits. Immunoblotting assays were used to determine the expression of vasodilator-stimulated phosphoprotein and Akt phosphorylation. A pulmonary metastasis experiment with male nude mice model was performed to test the effect of RSV on pulmonary metastasis and angiogenesis in vivo. Results RSV inhibited platelets-mediated angiogenic responses induced by adenosine diphosphate (ADP)ADP through increased cGMP generation and cGMP-mediated vasodilator-stimulated phosphoprotein phosphorylation along with reduced intracellular Ca2+ mobilization. In addition, RSV attenuated the platelet secretion and angiogenic responses induced by A549 cells in vitro and suppressed A549 lung cancer metastasis and angiogenesis in nude mice. Conclusions RSV is a potential therapeutic drug for the prevention of tumor metastasis by interrupting the platelet-tumor cell amplification loop.
ISSN:0022-4804
1095-8673
DOI:10.1016/j.jss.2017.05.009