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作 者:周鹏飞[1] 王大文[1] 南存金[1] 吴铁林[1] 杨森[1] 陈映鹤[1]
机构地区:[1]温州医学院附属第二医院泌尿外科,325027
出 处:《中华实验外科杂志》2014年第6期1228-1230,共3页Chinese Journal of Experimental Surgery
基 金:浙江省中医药管理局资助项目(2011ZB092);浙江省卫生厅医药卫生基金资助项目(2012KYB134)
摘 要:目的观察小干扰RNA(siRNA)沉默促肝细胞再生磷酸酶-3(PRL-3)基因对人雄激素依赖性前列腺癌(LNCaP)细胞增殖及凋亡的影响。方法应用靶向PRL-3基因小干扰RNA转染处理前列腺癌LNCaP细胞后,采用逆转录-聚合酶链反应(RT—PCR)和Westernblot检测PRL-3mRNA和蛋白水平,采用细胞计数试剂盒(CCK-8)检测细胞体外增殖能力,采用流式细胞仪检测细胞凋亡水平。结果与对照组比较,siRNA转染组PRL.3mRNA和蛋白水平明显下调,且呈浓度依赖性(P〈0.05)。体外实验显示,低浓度PRL-3siRNA对LNCaP细胞体外增殖能力没有影响,而中、高浓度PRL-3siRNA转染48h后明显地抑制LNCaP细胞的体外增殖能力(P〈0.05),低、中、高浓度siRNA沉默PRL-3基因后体外LNCaP细胞的凋亡率分别为(28.1±3.8)%、(25.2±2.5)%、(27.1±0.7)%(P〈0.05)。结论下调PRL-3基因的表达可抑制LNCaP细胞的增殖并促进LNCaP细胞的凋亡,PRL-3基因在前列腺癌LNCaP细胞体外增殖及凋亡中起重要作用。Objective To study the effects of small interfering RNA (siRNA) silencing phosphatase of regenerating liver cell 3 (PRL-3) on proliferation and apoptosis of human prostate cancer LNCaP cells. Methods After prostate cancer LNCaP cells were transfected by PRL-3 siRNA, the mRNA and protein of PRL-3 were detected by reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blotting, respectively. The growth of LNCaP cells was exmined by cell counting kit-8 (CCK-8). Flow eytometry was used to detect apoptosis. Results The siRNA could downregulate the mRNA and protein expression level of PRL-3 in a dose-dependent manner ( P 〈 0. 05). Low doses of PRL-3 siRNA did not affect the proliferation of LNCaP cells, but 100 nmol/L PRL-3 siRNA could effectively inhibit the proliferation of LNCaP ceils after 48 h in vitro ( P 〈 0. 05 ). Apoptosis rate of LNCaP ceils with low, middle and high PRL-3 siRNA interventions in vitro was (28.1 ± 3.8 ) %, ( 25.2 ± 2. 5 ) %, and (27. 1 ± 0. 7 ) % respectively ( P 〈 0. 05 ). Conclusion Downregulating PRL-3 could inhibit proliferation of LNCaP cells and promote apoptosis of LNCaP cells. PRL-3 gene might play an important role in proliferation and apoptosis of LNCaP cells.
关 键 词:前列腺癌 肝细胞再生磷酸酶-3 RNA干扰
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