LIU Xin 1, DENG Guo-ying 1, YANG Shu-feng 1, et al. Inhibition study of G31P,a chemokine receptor CXCR1/2 antagonist,in proliferation of human prostate cancer cells in vivo and in vitro. [J]. Journal of Chongqing Medical University 36(12):1420-1422(2011)
LIU Xin 1, DENG Guo-ying 1, YANG Shu-feng 1, et al. Inhibition study of G31P,a chemokine receptor CXCR1/2 antagonist,in proliferation of human prostate cancer cells in vivo and in vitro. [J]. Journal of Chongqing Medical University 36(12):1420-1422(2011)DOI:
Inhibition study of G31P,a chemokine receptor CXCR1/2 antagonist,in proliferation of human prostate cancer cells in vivo and in vitro
目的:探讨CXCR1/CXCR2受体拮抗剂-G31P对人前列腺癌细胞PC-3增殖的体内外抑制作用。方法:采用CCK-8法研究不同浓度G31P对PC-3细胞体外增殖的抑制作用。建立体内绿色荧光蛋白(Green fluorescent protein
GFP)标记人雄激素非依赖性前列腺癌细胞PC-3裸鼠原位移植瘤模型
观察G31P对裸鼠前列腺癌原位移植瘤的体积、重量的影响。结果:CCK-8结果显示100 ng/ml G31P与对照组相比分别作用1、3 d和5 d差异具有统计学意义(1 d P=0.007、3 d P=0.001、5 d P=0.028
均为P<0.05)。前列腺癌PC-3细胞裸鼠模型体内实验显示
与对照组(100μl N.S)相比
G31P处理组(0.5 mg/kg)从给药第18天起能显著抑制前列腺肿瘤的体积(P=0.026
P<0.05);与对照组相比G31P处理组在抑制前列腺肿瘤重量方面有明显作用(P=0.027
P<0.05)。结论:G31P体内外实验均能抑制人雄激素非依赖性前列腺癌细胞系PC-3的增殖。
Abstract
Objective:To investigate the effect of G31P on the proliferation of the prostate cancer in vivo and in vitro.Methods:The inhibition effect of G31P on the proliferation of PC-3 cell was investigated by CCK-8 assay in vitro.The effect of G31P on the volume and weight of human prostate tumor of nude mice was observed by building orthotopic transplantation tumor model of human androgen-independent prostate cancer PC-3(GFP-labeled) in nude mice.Results:CCK-8 assay found statistically significant difference in inhibiting the proliferation of PC-3 cells between the 100 ng/ml G31P and control group for 1 day(P<0.01)
3 days(P≤0.01) and 5 days(P<0.05).G31P treatment after the 18th day of administration inhibited significantly the prostate tumor volume compared with control group(P<0.05)
and this inhibition was more obvious(P<0.01) after the 24th day of administration in nude mice in vivo.A significant difference was observed between G31P treatment group(P<0.05) and the control group in prostate tumor weight.Conclusion:G31P can inhibit the proliferation of the prostate cancer in vivo and in vitro.