首页> 外文期刊>Japanese Journal of Cancer Research >Quantitative Measurement of Thymidylate Synthase and Dihydropyrimidine Dehydrogenase mRNA Level in Gastric Cancer by Real-time RT-PCR.
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Quantitative Measurement of Thymidylate Synthase and Dihydropyrimidine Dehydrogenase mRNA Level in Gastric Cancer by Real-time RT-PCR.

机译:实时RT-PCR定量测定胃癌中胸苷酸合酶和二氢嘧啶脱氢酶mRNA的水平。

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摘要

We used real-time reverse-transcription polymerase chain reaction (RT-PCR) to assay expression of the mRNA of thymidylate synthase (TS) and dihydropyrimidine dehydrogenase (DPD) in gastric cancer tissue with the objective of establishing a system to measure TS and DPD in ultra-low-volume samples. Nude mouse xenografts of 5 human gastric cancer cell lines and 85 clinical samples were used as the specimens in this study. Sensitivity to 5-fluorouracil (5-FU) was determined on the basis of the relative tumor proliferation rate in mice and the results of ATP assay using serum-free cultures of the clinical samples. mRNA expression was measured in tumor tissue by real-time RT-PCR using the ABI PRISM 7700 system. The values for expression of the mRNA for TS and DPD were corrected according to the level of glyceraldehyde-3-phosphate dehydrogenase mRNA expression. The xenografts yielded correlations between TS and DPD mRNA expression and the activity of the enzymes (TS: rs = 0.700, DPD: rs = 0.900), and an
机译:我们使用实时逆转录聚合酶链反应(RT-PCR)来检测胃癌组织中胸苷酸合酶(TS)和二氢嘧啶脱氢酶(DPD)mRNA的表达,目的是建立一个测量TS和DPD的系统在超少量样品中本研究使用了5种人类胃癌细胞系和85种临床样品的裸鼠异种移植物作为标本。根据小鼠的相对肿瘤增殖率和使用临床样品的无血清培养物进行的ATP测定结果,确定对5-氟尿嘧啶(5-FU)的敏感性。使用ABI PRISM 7700系统通过实时RT-PCR测量肿瘤组织中的mRNA表达。根据甘油醛-3-磷酸脱氢酶mRNA表达水平来校正TS和DPD的mRNA表达值。异种移植产生TS和DPD mRNA表达与酶活性之间的相关性(TS:rs = 0.700,DPD:rs = 0.900),并且

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