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Liu Xin, Dai Xiaodong, Li Xingyun, Wang Xiaoli, Li Fang. Inhibition of G31P:Chemokine Receptor CXCR1/CXCR2 Antagonist,in Angiogenesis of Human Prostate Cancer Cells in vivo[J]. Cancer Research on Prevention and Treatment, 2012, 39(07): 784-786. DOI: 10.3971/j.issn.1000-8578.2012.07.006
Citation: Liu Xin, Dai Xiaodong, Li Xingyun, Wang Xiaoli, Li Fang. Inhibition of G31P:Chemokine Receptor CXCR1/CXCR2 Antagonist,in Angiogenesis of Human Prostate Cancer Cells in vivo[J]. Cancer Research on Prevention and Treatment, 2012, 39(07): 784-786. DOI: 10.3971/j.issn.1000-8578.2012.07.006

Inhibition of G31P:Chemokine Receptor CXCR1/CXCR2 Antagonist,in Angiogenesis of Human Prostate Cancer Cells in vivo

  • Objective To investigate the inhibition of G31P on the angiogenesis of the prostate cancer PC-3 cell in vivo. Methods The effect of G31P on angiogenesis of human prostate tumor of nude mice were observed in nude mice by building a human androgen-independent prostate cancer PC-3 (GFP-labeled) orthotopic transplantation tumor cells model. Results The tumor angiogenesis of G31P treated group (1.26±0.46)was significantly reduced (0.49±0.12,P<0.05) compared with the control group.VEGF(P<0.01)and NF-κB(P<0.01)expression of G31P treated groupwas significantly reduced (immunohistochemistry) compared with the control group. Conclusion G31P could inhibit the angiogenesis of the prostate cancer PC-3 cell in vivo.
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