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Comparison of gene expression profiling by reverse transcription quantitative PCR between fresh frozen and formalin-fixed, paraffin-embedded breast cancer tissues

机译:新鲜冷冻和福尔马林固定,石蜡包埋的乳腺癌组织之间通过逆转录定量PCR进行的基因表达谱比较

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摘要

Recent reports demonstrate the feasibility of quantifying gene expression by using RNA isolated from blocks of formalin-fixed, paraffin-embedded (FFPE) tumor tissue. The development of molecular tests for clinical use based on archival materials would be of great utility in the search for and validation of important genes or gene expression profiles. In this study, we compared the performance of different normalization strategies in the correlation of quantitative data between fresh frozen (FF) and FFPE samples and analyzed the parameters that characterize such correlation for each gene. Total RNA extracted from FFPE samples presented a shift in raw cycle threshold (Cq) values that can be explained by its extensive degradation. Proper normalization can compensate for the effects of RNA degradation in gene expression measurements. We show that correlation between normalized expression values is better for moderately to highly expressed genes whose expression varies significantly between samples. Nevertheless, some genes had no correlation. These genes should not be included in molecular tests for clinical use based on FFPE samples. Our results could serve as a guide when developing clinical diagnostic tests based on RT-qPCR analyses of FFPE tissues in the coming era of treatment decision-making based on gene expression profiling.
机译:最近的报道证明了通过使用从福尔马林固定的石蜡包埋的(FFPE)肿瘤组织块中分离的RNA定量基因表达的可行性。基于档案材料的临床分子检测的开发将对重要基因或基因表达谱的寻找和验证具有巨大的实用性。在这项研究中,我们比较了新鲜冰冻(FF)和FFPE样品之间定量数据相关性中不同归一化策略的性能,并分析了每个基因表征此类相关性的参数。从FFPE样品中提取的总RNA出现了原始循环阈值(Cq)值的变化,这可以用其大量降解来解释。适当的归一化可以补偿基因表达测量中RNA降解的影响。我们表明,中度至高度表达的基因的标准化表达值之间的相关性更好,它们之间的表达差异很大。然而,一些基因没有相关性。这些基因不应包括在基于FFPE样品的临床分子检测中。我们的结果可作为在基于基因表达谱的治疗决策时代基于FFPE组织的RT-qPCR分析开发临床诊断测试时的指南。

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