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利用功能验证的反转录实时定量 PCR 分析方法进行生物标志物研究和早期药物开发中的基因表达分析。

Gene expression analysis in biomarker research and early drug development using function tested reverse transcription quantitative real-time PCR assays.

机构信息

Roche Applied Science, Roche Diagnostics GmbH, Penzberg, Germany.

出版信息

Methods. 2013 Jan;59(1):10-9. doi: 10.1016/j.ymeth.2012.07.003. Epub 2012 Jul 14.

Abstract

The identification of new biomarkers is essential in the implementation of personalized health care strategies that offer new therapeutic approaches with optimized and individualized treatment. In support of hypothesis generation and testing in the course of our biomarker research an online portal and respective function-tested reverse transcription quantitative real-time PCR assays (RT-qPCR) facilitated the selection of relevant biomarker genes. We have established workflows applicable for convenient high throughput gene expression analysis in biomarker research with cell lines (in vitro studies) and xenograft mouse models (in vivo studies) as well as formalin-fixed paraffin-embedded tissue (FFPET) sections from various human research and clinical tumor samples. Out of 92 putative biomarker candidate genes selected in silico, 35 were shown to exhibit differential expression in various tumor cell lines. These were further analysed by in vivo xenograft mouse models, which identified 13 candidate genes including potential response prediction biomarkers and a potential pharmacodynamic biomarker. Six of these candidate genes were selected for further evaluation in FFPET samples, where optimized RNA isolation, reverse transcription and qPCR assays provided reliable determination of relative expression levels as precondition for differential gene expression analysis of FFPET samples derived from projected clinical studies. Thus, we successfully applied function tested RT-qPCR assays in our biomarker research for hypothesis generation with in vitro and in vivo models as well as for hypothesis testing with human FFPET samples. Hence, appropriate function-tested RT-qPCR assays are available in biomarker research accompanying the different stages of drug development, starting from target identification up to early clinical development. The workflow presented here supports the identification and validation of new biomarkers and may lead to advances in efforts to achieve the goal of personalized health care.

摘要

鉴定新的生物标志物对于实施个性化医疗保健策略至关重要,这些策略提供了新的治疗方法,具有优化和个体化的治疗效果。为了支持我们的生物标志物研究中的假设生成和测试,我们建立了一个在线门户和相应的经过功能测试的反转录定量实时 PCR 检测(RT-qPCR),以方便选择相关的生物标志物基因。我们已经建立了适用于细胞系(体外研究)和异种移植小鼠模型(体内研究)以及各种人类研究和临床肿瘤样本的福尔马林固定石蜡包埋组织(FFPET)切片的高通量基因表达分析的工作流程。在 92 个潜在的生物标志物候选基因中,有 35 个在各种肿瘤细胞系中表现出差异表达。这些基因进一步通过体内异种移植小鼠模型进行分析,鉴定出 13 个候选基因,包括潜在的反应预测生物标志物和潜在的药效学生物标志物。其中 6 个候选基因被选中用于进一步在 FFPET 样本中进行评估,其中优化的 RNA 分离、反转录和 qPCR 检测为 FFPET 样本的差异基因表达分析提供了可靠的相对表达水平的测定,这些样本来自预计的临床研究。因此,我们成功地将经过功能测试的 RT-qPCR 检测应用于我们的生物标志物研究中,用于体外和体内模型的假设生成以及人类 FFPET 样本的假设测试。因此,在药物开发的不同阶段,从靶点鉴定到早期临床开发,都有适当的经过功能测试的 RT-qPCR 检测用于生物标志物研究。本工作流程支持新的生物标志物的鉴定和验证,并可能有助于实现个性化医疗保健目标的努力。

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