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Evaluation and validation of candidate endogenous control genes for real-time quantitative PCR studies of breast cancer

机译:乳腺癌实时定量PCR研究的候选内源性对照基因的评估和验证

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摘要

BackgroundReal-time quantitative PCR (RQ-PCR) forms the basis of many breast cancer biomarker studies and novel prognostic assays, paving the way towards personalised cancer treatments. Normalisation of relative RQ-PCR data is required to control for non-biological variation introduced during sample preparation. Endogenous control (EC) genes, used in this context, should ideally be expressed constitutively and uniformly across treatments in all test samples. Despite widespread recognition that the accuracy of the normalised data is largely dependent on the reliability of the EC, there are no reports of the systematic validation of genes commonly used for this purpose in the analysis of gene expression by RQ-PCR in primary breast cancer tissues. The aim of this study was to identify the most suitable endogenous control genes for RQ-PCR analysis of primary breast tissue from a panel of eleven candidates in current use. Oestrogen receptor alpha (ESR1) was used a target gene to compare the effect of choice of EC on the estimate of gene quantity.
机译:背景技术实时定量PCR(RQ-PCR)构成了许多乳腺癌生物标志物研究和新型预后分析的基础,为个性化癌症治疗铺平了道路。需要对相对RQ-PCR数据进行标准化,以控制样品制备过程中引入的非生物变异。在本文中,内源性对照(EC)基因理想地应在所有测试样品的所有处理中组成性且均匀地表达。尽管人们普遍认识到标准化数据的准确性在很大程度上取决于EC的可靠性,但尚无关于通过RQ-PCR分析原发性乳腺癌组织中基因表达的系统验证基因的报告。这项研究的目的是从目前使用的11种候选药物中鉴定出最合适的内源性对照基因,用于原发性乳腺组织的RQ-PCR分析。使用雌激素受体α(ESR1)作为靶基因,比较EC选择对基因数量估计的影响。

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