首页> 美国卫生研究院文献>The Journal of Molecular Diagnostics : JMD >Quantitative mRNA Expression Analysis from Formalin-Fixed Paraffin-Embedded Tissues Using 5′ Nuclease Quantitative Reverse Transcription-Polymerase Chain Reaction
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Quantitative mRNA Expression Analysis from Formalin-Fixed Paraffin-Embedded Tissues Using 5′ Nuclease Quantitative Reverse Transcription-Polymerase Chain Reaction

机译:使用5核酸酶定量逆转录聚合酶链反应从福尔马林固定石蜡包埋的组织中定量mRNA表达分析

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摘要

Analysis of gene expression and correlation with clinical parameters has the potential to become an important factor in therapeutic decision making. The ability to analyze gene expression in archived tissues, for which clinical followup is already available, will greatly facilitate research in this area. A major obstacle to this approach, however, has been the uncertainty about whether gene expression analyses from routinely archived tissues accurately reflect expression before fixation. In the present study we have optimized the RNA isolation and reverse transcription steps for quantitative reverse transcription-polymerase chain reaction (RT-PCR) on archival material. Using tissue taken directly from the operating room, mRNAs with half-lives from 10 minutes to >8 hours were isolated and reverse transcribed. Subsequent real-time quantitative PCR methodology (TaqMan) on these cDNAs gives a measurement of gene expression in the fixed tissues comparable to that in the fresh tissue. In addition, we simulated routine pathology handling and demonstrate that this method of mRNA quantitation is insensitive to pre-fixation times (time from excision to fixation) of up to 12 hours. Therefore, it should be feasible to analyze gene expression in archived tissues where tissue collection procedures are largely unknown.
机译:基因表达及其与临床参数的相关性分析有可能成为治疗决策的重要因素。已经进行了临床随访的分析存档组织中基因表达的能力将极大地促进这一领域的研究。然而,该方法的主要障碍是不确定来自常规存档组织的基因表达分析是否能准确反映固定前的表达。在本研究中,我们针对档案材料上的定量逆转录聚合酶链反应(RT-PCR)优化了RNA分离和逆转录步骤。使用直接取自手术室的组织,将半衰期从10分钟到> 8小时的mRNA进行分离并逆转录。随后对这些cDNA进行的实时定量PCR方法(TaqMan)可以测量固定组织中的基因表达,其程度与新鲜组织中的表达相当。此外,我们模拟了常规病理处理,并证明了这种mRNA定量方法对长达12小时的预固定时间(从切除到固定的时间)不敏感。因此,在很大程度上未知组织收集程序的存档组织中分析基因表达应该是可行的。

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