摘要
目的:探讨泌乳素相关蛋白(PIP)在前列腺癌不同细胞系中的表达情况,以及雄激素对其表达的影响。方法:应用不同浓度(0、0.1、1、10、100nmol/L)双氢睾酮(Dihydrotestosterone,DHT)或睾酮(Testosterone,T)及不同时间(6、24和48h)对前列腺癌细胞系(LNCaP、PC-3、DU145)及人乳腺癌细胞系T47D进行处理,通过RT-PCR及实时荧光定量PCR法检测PIP及雄激素受体(AR)mRNA表达情况。通过Westernblot法检测各细胞系(LNCaP、PC-3、DU145、T47D)中PIP蛋白表达情况。结果:雄激素依赖性前列腺癌细胞系LNCaP中有PIP mRNA及蛋白表达,PI P mRNA的表达随DHT或T浓度增加而增加,且于10nmol/L浓度DHT或T时达到最大峰值。而AR mRNA的表达差异无统计学意义。雄激素非依赖性前列腺癌细胞系PC-3与DU145中无PIP mRNA及蛋白表达,并且AR表达较少或无AR表达。结论:PIP在前列腺癌发生发展机制中,以及鉴别前列腺癌是否具有雄激素依赖性方面有一定作用。
Objective: To determine prolactin-inducible protein (PIP) mRNA expression and effects of androgen in human prostate cancer cell lines. Methods: Prostate cell hnes (LNCaP, PC-3, DU145) and breast tumor cell line (T47D) were treated by different concentrations (0, 0.1, 1, 10 and 100 nmol/L) and different times (6, 24 and 48 h) of dihydrotestosterone (DHT) or testosterone (T). The PIP and androgen receptor (AR) mRNA expressions were detected by RT-PCR. The PIP protein expression was determined by Western blot in four cell lines. Results: By RT-PCR and Western blot, PIP mRNA and protein expression were found in androgen-dependent prostate cancer cell line LNCaP. PIP mRNA expression was increased along with concentrations of DHT or T in LNCaP. PIP mRNA level reached maximum peak in 10 nmol/L DHT or T. There was no significant difference in AR mRNA expression. There were no PIP mRNA and protein expressions in androgen-independent prostate cancer cell lines PC-3 and DU145. Conclusion: The role of PIP may occur in the process of development of prostate cancer, and in the differentialdiagnosis of prostate cancer for the androgen dependence.
出处
《天津医药》
CAS
北大核心
2012年第11期1110-1113,共4页
Tianjin Medical Journal
基金
河北省卫生厅重点课题计划(项目编号:20090543)
关键词
前列腺肿瘤
雄激素类
催乳素
前列腺特异抗原
睾酮
双氢睾酮
聚合酶链反应
prostatic neoplasms androgens prolactin prostate-specific antigen testosterone dihydrotestosteronepolymerase chain reaction