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硫化氢抑制前列腺癌骨转移PC-3细胞增殖和侵袭的体外研究
引用本文:黄新宇,杨远良,许国华,容锡沧,冯瑞强. 硫化氢抑制前列腺癌骨转移PC-3细胞增殖和侵袭的体外研究[J]. 中国医药导报, 2013, 10(23): 24-27
作者姓名:黄新宇  杨远良  许国华  容锡沧  冯瑞强
作者单位:黄新宇 (广东省江门市人民医院骨科,广东江门,529000); 杨远良 (广州市番禺区中心医院骨一科,广东广州,511400); 许国华 (广东省江门市人民医院骨科,广东江门,529000); 容锡沧 (广东省江门市人民医院骨科,广东江门,529000); 冯瑞强 (广东省江门市人民医院骨科,广东江门,529000);
摘    要:目的探讨硫化氢对前列腺癌骨转移PC-3细胞增殖和侵袭的影响及其可能机制。方法分别用0、1、2、4 mmol/LNaHS(硫化氢载体)作用前列腺癌骨转移PC-3细胞36 h,CCK-8比色法法检测细胞存活率,transwell法检测细胞侵袭能力,ELISA法检测细胞MMP-2和MMP-9分泌能力,Western-Blot法检测Bcl-2、Bax蛋白的表达。结果硫化氢对PC-3细胞生长的影响:用硫化氢孵育PC-3细胞36 h,1.0 mmol/L NaHS组细胞存活率与对照组比较,差异无统计学意义(P〉0.05);2、4 mmol/L NaHS作用PC-3细胞36 h,细胞存活率降低,与对照组比较,能不同程度抑制PC-3细胞的生长,差异有统计学意义(P〈0.05或P〈0.01)。硫化氢对PC-3细胞侵袭的影响:用硫化氢孵育PC-3细胞36 h,1 mmol/L NaHS组细胞侵袭数与对照组比较,差异无统计学意义(P〉0.05);2、4 mmol/L NaHS作用PC-3细胞36 h,细胞侵袭数减少,与对照组比较,能不同程度抑制PC-3细胞的侵袭,差异有统计学意义(P〈0.05或P〈0.01)。ELISA法检测PC-3细胞MMP-2和MMP-9分泌能力:用硫化氢孵育PC-3细胞36 h,1 mmol/L NaHS组细胞MMP-2和MMP-9分泌量与对照组比较,差异无统计学意义(P〉0.05);2、4 mmol/L NaHS作用PC-3细胞36 h,MMP-2和MMP-9分泌量减少,与对照组比较,能不同程度抑制PC-3细胞MMP-2和MMP-9的分泌,差异有统计学意义(P〈0.05或P〈0.01)。Western blot检测PC-3细胞Bcl-2/Bax蛋白表达:1、2、4 mmol/L NaHS组,Bcl-2表达降低,Bax表达升高,呈浓度依赖性。结论 2 mmol/L浓度以上的NaHS能影响Bcl-2和Bax表达和MMP-2 MMP-9分泌来抑制PC-3细胞的生长和侵袭。

关 键 词:硫化氢  前列腺癌  骨转移  PC-3细胞  增殖  侵袭

Invitrostudy of hydrogen sulfide inhibits proliferation and invasion of prostate cancer bone metastasis PC-3 cells
HUANG Xinyu,YANG Yuanliang,XU Guohua,RONG Xicang,FENG Ruiqiang. Invitrostudy of hydrogen sulfide inhibits proliferation and invasion of prostate cancer bone metastasis PC-3 cells[J]. China Medical Herald, 2013, 10(23): 24-27
Authors:HUANG Xinyu  YANG Yuanliang  XU Guohua  RONG Xicang  FENG Ruiqiang
Affiliation:1.Department of Orthopedic,the People's Hospital of Jiangmen City,Guangdong Province,Jiangmen 529000,China;2.The First Department of Orthopedic,Guangzhou Panyu Central Hospital,Guangdong Province,Guangzhou 511400,China
Abstract:Objective To investigate the effect of hydrogen sulfide on prostate cancer bone metastasis PC-3 cells pro liferation and invasion in vitro and the possible mechanism.Methods PC-3 cells were treated with NaHS(a donor of hydrogen sulfide) at 0,1,2,4 mmol/L concentration for 36 h,respectively,then cell viability was tested by cell counter kit-8.Transwell assay were used to detect PC-3 cells invasive ability and ELISA was used to detect MMP-2 and MMP-9 secretion.PC-3 cells were treated with NaHS at 0,1,2,4 mmol/L concentration for 36 h,then the ex pressions of Bcl-2,Bax were evaluated by Western-Blot assay.Results The effects of hydrogen sulfide on PC-3 cells proliferation: the differences of cell viabilitie were not significant(P 0.05) when PC-3 cells were treated with NaHS at 1 mmol/L concentrations.When PC-3 cells were treated with NaHS at 2,4 mmol/L concentration,the cell viability was declined,compare with control group(P 0.05,P 0.01).The effects of hydrogen sulfide on PC-3 cells invasive: the numbers of transfer to the other side of transwell membrane were counted in tumor invasive assay.The difference of 1 mmol/L NaHS group was not significant compared with control group(P 0.05) and 2 mmol/L NaHS group and 4 mmol/L NaHS group were declined compared with control group(P 0.05 or P 0.01).The effect of hydrogen sulfide on MMP-2 and MMP-9 secretion: when cells were treated by 1 mmol/L NaHS,the secretion of MMP-2 and MMP-9 was not significant compared with control group(P 0.05),2 mmol/L NaHS group and 4 mmol/L NaHS group were declined of MMP-2 and MMP-9 secretion compared with control group(P 0.05 or P 0.01).The effects of hydrogen sulfide on PC-3 cells Bcl-2 and Bax expression: the expression of Bcl-2 was declined and Bax expression in creased compare with control group.Conclusion Hydrogen sulfide can inhibit the growth and invasive of PC-3 cells at the concentration 2,4 mmol/L by affecting Bcl-2 and Bax expression and reducing secretion of MMP-2 and MMP-9.
Keywords:Hydrogen sulfide  Prostate cancer  Bone metastasis  PC-3 cells  Proliferation  Invasion
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