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Expression of the catalytic subunit associated with telomerase gene in human urinary bladder cancer (see comments)

机译:与端粒酶基因相关的催化亚基在人膀胱癌中的表达(见评论)

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PURPOSE: Telomerase is the ribonucleoprotein enzyme associated with the immortalization and oncogenesis of cancer cells. To examine the expression of two major components of the telomerase associated gene, hEST2/hTRT and TLP1/TP1, in urinary bladder carcinogenesis, we studied 27 human urinary bladder cancers using the reverse transcriptase-polymerase chain reaction (RT-PCR) method. MATERIALS AND METHODS: Total RNAs were obtained from 27 urinary bladder cancer and 23 normal bladder tissues using surgical removal or the cold cup bioptical method. The cDNA was then synthesized from these total RNAs, and hTRT and TP1 mRNA were amplified using the RT-PCR method. RESULTS: hEST2/hTRT expression was detected in all 27 (100%) cases. However, TLP1/TP1 was detected in 25 of 27 (93%) cases. The correlation between these expressions and clinicopathological characteristics such as tumor grade, clinical stage, and histological type showed no statistical significance. Twenty-three cases of normal bladder tissues showed no expression of hEST2/hTRT, but 18 of 23 (78%) cases showed TLP1/TP1 expression. CONCLUSIONS: These findings indicate that the up-regulation of hEST2/hTRT gene expression may play a critical role in carcinogenesis of human urinary bladder cancers. RT-PCR for detecting expression of hEST2/hTRT gene is a powerful method for the screening and diagnosis of urinary bladder cancer.
机译:目的:端粒酶是与癌细胞永生化和肿瘤发生有关的核糖核糖核酸酶。为了检查端粒酶相关基因hEST2 / hTRT和TLP1 / TP1的两个主要成分在膀胱癌发生中的表达,我们使用逆转录聚合酶链反应(RT-PCR)方法研究了27例人类膀胱癌。材料与方法:采用手术切除或冷杯活检法从27例膀胱癌和23例正常膀胱组织中获得总RNA。然后从这些总RNA合成cDNA,并使用RT-PCR方法扩增hTRT和TP1 mRNA。结果:在所有27例(100%)病例中均检测到hEST2 / hTRT表达。但是,在27例病例中有25例(93%)检测到TLP1 / TP1。这些表达与临床病理特征如肿瘤等级,临床分期和组织学类型之间的相关性无统计学意义。 23例正常膀胱组织未显示hEST2 / hTRT表达,但23例中有18例(78%)显示TLP1 / TP1表达。结论:这些发现表明,hEST2 / hTRT基因表达的上调可能在人类膀胱癌的致癌作用中起关键作用。 RT-PCR检测hEST2 / hTRT基因表达是一种强有力的膀胱癌筛查和诊断方法。

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