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作 者:王海峰[1,2] 刘武江[1,2] 金杰[1,2] 周利群[1,2] 梁丽莉[1,2] 王莹[1,2] 郭应禄[1,2]
机构地区:[1]北京大学第一医院泌尿外科 [2]北京大学泌尿外科研究所国家泌尿男性生殖系肿瘤研究中心,北京100034
出 处:《北京大学学报(医学版)》2011年第4期490-495,共6页Journal of Peking University:Health Sciences
基 金:国家自然科学基金项目(30772168)资助~~
摘 要:目的:研究雄激素受体(androgen receptor,AR)在激素依赖性前列腺癌(androgen dependent prostate can-cer,ADPC)细胞系LNCaP转化成激素非依赖性前列腺癌(androgen independent prostate cancer,AIPC)过程中的表达变化,以及其受Wnt信号通路和蛋白酶体降解通路调控的机制。方法:应用活性炭滤过的低激素胎牛血清培养LNCaP细胞,得到雄激素非依赖的LNCaP亚系LNCaP-AI(androgen independent)细胞。应用细胞增殖试验检测LNCaP-AI的细胞生长曲线。应用Western blot、RT-PCR分析激素依赖性转化过程中的AR、前列腺特异抗原(pros-tate specific antigen,PSA)的表达变化。在AIPC细胞中,应用Wnt信号通路阻滞剂IWR-1及蛋白酶体通路抑制剂乳胞素(lactacystin)处理细胞,观察Wnt信号通路和蛋白酶体信号通路对AR mRNA及蛋白表达的影响。结果:在体外低激素环境中生长6个月后,LNCaP细胞变成雄激素非依赖性的LNCaP亚系LNCaP-AI。表现为对雄激素依赖性减弱,细胞增殖加快,PSA的表达增高。在转化为LNCaP-AI的过程中,AR mRNA水平短期上调,后恢复到原始水平,但蛋白水平一直处于下调趋势。IWR-1处理的LNCaP-AI,AR mRNA及蛋白的表达下调。乳胞素处理的LNCaP-AI,AR mRNA无变化而蛋白表达上调。结论:在体外前列腺癌细胞由激素依赖性向非依赖性转化的过程中,AR mRNA表达仅有一过性增高,而蛋白表达呈现明显的下降趋势。进一步研究发现,Wnt信号通路和蛋白酶体通路可能对AR的蛋白表达有调控作用。Wnt信号通路的抑制或蛋白酶体信号通路的增强可能是AR蛋白表达下调的原因。Objective: To investigate the expression and regulation of androgen receptor(AR) in prostate cancer cells from androgen dependent to androgen independent.Methods: LNCaP cells were cultured in charcoal-stripped serum for 6 months to establish androgen-independent celline(LNCaP-AI).Proliferation of LNCaP-AI was assayed by cell viability.Expression of AR mRNA and protein was analyzed by RT-PCR and Western blot.Wnt signaling pathway inhibitor IWR-1 and proteasome inhibitor lactacystin were used to investigate effects of Wnt and proteasome pathway on AR expression in LNCaP-AI.Results: LNCaP-AI exhibit enhanced proliferation and up-regulated PSA expression compared with LNCaP.During androgen deprivation,AR mRNA was up-regulated in a short early stage and then declined to a stable level in LNCaP-AI compared with LNCaP,but AR protein kept in downward trend.The mRNA and protein expression of AR was decreased by IWR-1 treatment.AR protein but not mRNA was increased by lactacystin treatment.Conclusion: The androgen independent prostate cancer cellline was established by androgen deprivation,in which the protein expression of AR was dramatically decreased.mRNA and protein expression of AR in LNCaP-AI was related to Wnt signaling pathway and proteasome pathway.Increased Wnt signaling or decreased proteasome pathways contribute the decreased AR protein expression.
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