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胶质瘤细胞系T98G、U87和U251中CYP17A1的表达及意义

Expression of CYP17A1 in glioma cell lines T98G,U87 and U251 and its significance
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摘要 目的探讨细胞色素P450c17a酶(CYP17A1)在人神经胶质瘤细胞系T98G、U87和U251中的表达情况。方法采用Western blot和实时荧光定量PCR于蛋白质水平和mRNA水平检测细胞色素P450c17a酶(CYP17A1)在三种人胶质瘤细胞系中的表达。结果 Western blot检测出CYP17A1蛋白在胶质瘤细胞系T98G、U251和U87中的相对表达量为0.518±0.052、0.460±0.034和0.142±0.025。T98G和U251的CYP17A1蛋白表达水平明显高于U87,差异有统计学意义(P<0.05)。实时荧光定量PCR检测结果显示CYP17A1的mRNA在T98G、U251和U87中相对转录水平为1.000±0.122、0.960±0.079、0.611±0.045,T98G和U251细胞中CYP17A1的mRNA转录水平均高于U87,差异有统计学意义(P<0.05)。同时Western blot和实时荧光定量PCR都指出T98G和U251在CYP17A1在蛋白和mRNA的表达上无统计学差异(P>0.05)。结论人胶质瘤细胞系T98G和U251中CYP17A1的表达量较高,这两种细胞系可作为良好的细胞模型用来研究CYP17A1在胶质瘤中的作用机制以及以CYP17A1为靶点的肿瘤治疗等。 Objective To investigate the expression of P450c17a(CYP17A1)in glioma cell lines T98G, U87 and U251. Methods The expression of CYP17A1 in human glioma cell lines T98G,U87 and U251 was detected by Western blot and Real-Time PCR. Results Western blot demonstrated that the expression of CYP17A1 was higher in T98G(0. 518±0. 052)and U251(0. 460±0. 034)than U87(0. 142±0. 025)(P〈0.05). Real-time fluorescent quantitative PCR analy- sis indicated that the positive expression of CYP17A1 in T98G, U87 and U251 cell lines were 1. 000±0. 122,0. 960±0. 079,0. 611±0. 045. CYP17A1 protein positive rate and m RNA levels in glioma cell lines T98G and U251 were significantly higher than that of U87(both P〈0.05). But CYP17A1 protein positive rate and m RNA levels were not significantly different between T98G and U251(P〉0.05). Conclusion CYP17A1 is highly-expressed in glioma cell lines T98G and U251,which can be used as an ideal cell model for the research of the role of CYP17A1 in glioma and the specific therapies targeting CYP17A1.
出处 《立体定向和功能性神经外科杂志》 2016年第6期344-347,共4页 Chinese Journal of Stereotactic and Functional Neurosurgery
基金 安徽省自然科学基金项目(编号:1408085MKL69) 脑功能与脑疾病安徽省重点实验室绩效考核补助项目(编号:1506c085017,1606c08235) 安徽省科技攻关项目(编号:1604a0802069)
关键词 胶质瘤 P450c17a酶 细胞系 免疫印迹 实时荧光定量PCR Glioma P450c17a(CYP17A1) Cell line Western blot Real-Time PCR
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