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作 者:谢蛟魁 宋印娥[1] 陈海文[2] 张胜茹[1] 田宏[3]
机构地区:[1]安康市中心医院泌尿外科,陕西安康725000 [2]西安交通大学第二附属医院泌尿外科,陕西西安710004 [3]西安交通大学生殖医学研究中心,陕西西安710061
出 处:《现代肿瘤医学》2017年第6期859-863,共5页Journal of Modern Oncology
摘 要:目的:观察双氢睾酮(DHT)和氟他胺(FLU)作用于雄激素依赖性前列腺癌细胞LNCa P内Ca^(2+)的变化,探讨DHT和FLU引起LNCa P细胞内Ca^(2+)变化的作用机制。方法:获得雄激素依赖性(LNCa P)细胞株,进行细胞培养,获得稳定生长及传代的细胞株。不同浓度的雄激素受体激动剂DHT及雄激素受体拮抗剂FLU作用于培养的LNCa P细胞株,不同时间点取干预措施下的LNCa P细胞,通过荧光染料负载,经流式细胞术检测并比较不同时间点、不同浓度药物作用下LNCa P细胞Ca^(2+)的变化和差异。结果:DHT作用于LNCa P细胞后,在每个剂量组中Ca^(2+)荧光强度差异有统计学意义(P<0.05),不同时间点变化差异有统计学意义(P<0.05)。FLU干预LNCa P后,各个剂量组的Ca^(2+)荧光强度随着时间的变化差异有统计学意义(P<0.05)。结论:DHT降低LNCa P细胞内Ca^(2+)含量不明显,说明对LNCa P细胞内的信号转导及凋亡影响不大;而FLU可明显提高LNCa P细胞内Ca^(2+)的浓度,导致钙超载,促进细胞的凋亡。Objective: To investigate the change of Ca^2+ and discuss the mechanism of Ca^2+ changes in LNCa P cells by DHT and FLU. Methods: To abtain drogen- dependent( LNCa P) prostate cancer cell lines,by cell culture,to abtain stable cell strains. The androgen receptor agonist DHT and the androgen receptor antagonist FLU acted on the culture prostate cancer cell line of androgen at different concentrations drugs. We extracted cells at different time points of LNCa P under the interventions. By fluorescent dye load measured,to compare the Ca^2+ differences at different time points and under the action of different drug concentrations in LNCa P by flow cytometry. Results: After DHT acts on LNCa P cells,the Ca^2+ of LNCa P increased significantly( P〈0. 05),but the difference of the increasing degree of each index in different time points. After FLU acts on LNCa P cells,the content of Ca^2+ increased significantly( P〈0. 05). Conclusion: The content of Ca^2+ is not obvious decreased in LNCa P cell by DHT,showed the low effect on signal transduction and the apoptosis. However,the concentration of Ca^2+ in LNCa P cells could be increased obviously by FLU,which leads to calcium overload and promotes cell apoptosis.
关 键 词:双氢睾酮 氟他胺 人前列腺癌细胞LNCaP细胞株 钙离子
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