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人前列腺癌细胞中肝X受体特异性激动剂GW3965对核受体结合蛋白1的影响
引用本文:杜晚林,杜媛,李克勤,陈江平,张仕强,陈燕. 人前列腺癌细胞中肝X受体特异性激动剂GW3965对核受体结合蛋白1的影响[J]. 现代医药卫生, 2012, 28(17): 2561-2563
作者姓名:杜晚林  杜媛  李克勤  陈江平  张仕强  陈燕
作者单位:[1]广安市岳池红十字川东医院,四川广安638300 [2]苏州虎丘医院,江苏苏州215008 [3]岳池县人民医院,四川广安638300 [4]岳池县疾病控制中心,四川广安638300
基金项目:国家自然科学基金资助项目(30901593)
摘    要:目的探讨人前列腺癌细胞系DU145细胞中肝X受体(liver X receptor,LXR)特异性激动剂GW3965对核受体结合蛋白1(nuclear receptor binding protein 1,NRBP1)的表达调控作用。方法采用MTT法检测不同浓度GW3965(浓度分别为0.5、5、10μmol/L)作用24 h后对DU145细胞增殖的影响。在人前列腺癌DU145细胞中用LXR的特异性激动剂GW3965处理24 h后,经逆转录-聚合酶链反应(RT-PCR)检测LXR特异性靶基因三磷腺苷结合A1(ATP-bindingcassette A1,ABCA1)转录水平的表达情况;随后在转录水平和翻译水平检测NRBP1的表达。结果 LXR特异性激动剂GW3965各实验组对细胞的活性和增殖无影响(P>0.05)。GW3965作用于DU145细胞后,ABCA1转录水平呈剂量依赖性升高,表明LXR在DU145细胞中具有功能活性。LXR经过活化后在转录和翻译水平对NRBP1的抑制作用呈剂量依赖性降低。结论 LXR在DU145细胞中可抑制NRBP1的表达。

关 键 词:前列腺肿瘤  细胞    受体,细胞表面/激动剂  受体,胞质和核  GW3965  核受体结合蛋白1

Effect of GW3965 on NRBP1 expression in prostate cancer cells
Du Wanlin,Du Yuan,Li Keqin,Chen Jiangping,Zhang Shiqiang,Chen Yan. Effect of GW3965 on NRBP1 expression in prostate cancer cells[J]. JOURNAL OF MODERN MEDICINE & HEALTH, 2012, 28(17): 2561-2563
Authors:Du Wanlin  Du Yuan  Li Keqin  Chen Jiangping  Zhang Shiqiang  Chen Yan
Affiliation:1. Yuechi Red Cross Chuandong Haspital , Guang' an , Sichuan 638300, China; 2. Huqiu Hospital, Suzhou, Jiangs u 215008, China; 3. Yueehi County People ' s Hospital, Guang ' an, Siehan 638300, China; 4. Yueehi County Center for Disease Control, Guang' an, Siehuan 638300, China)
Abstract:Objective To investigate the effect of liver X receptor(LXR) specific agonist GW3965 on the expression of nuclear receptor binding protein 1 (NRBPI) in DU145 cell line of prostate cancer. Methods The effect of various GW3965 concentrations (0.5,5,10 μmol/L) on the proliferation of DU145 cells was detected by the MTF test. DU 145 cells were treated with GW3965 for 24 h and then ATP-binding cassette A 1 (ABCA 1 ) mRNA was detected by RT-PCR;NRBP1 mRNA and protein were assayed by using RT-PCR and Western blot. Results GW3965 had no effect on the activity and proliferation of DU145 cells (P〉0.05). The level of ABCA 1 mRNA was close-dependently increased, after treating DU 145 cells with different concentrations of GW3965 for 24 h respectively, which demonstrated that LXR had the functional activity in DU145. NRBP1 were down- regulated in both mRNA and protein level after LXR activation. Conclusion LXR could inhibit the expression of NRBP1 in DU145 cells.
Keywords:Prostatic neoplasms  Cells  Liver  Receptors,cell surface/agonists  Receptors,cytoplasmic and nu-c|e~r: GW3965  Nuclear receptor binding protein 1
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