Literature DB >> 22796720

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

Sabine Lohmann1, Andrea Herold, Tobias Bergauer, Anton Belousov, Gisela Betzl, Mark Demario, Manuel Dietrich, Leopoldo Luistro, Manuela Poignée-Heger, Kathy Schostack, Mary Simcox, Heiko Walch, Xuefeng Yin, Hua Zhong, Martin Weisser.   

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.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22796720     DOI: 10.1016/j.ymeth.2012.07.003

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  4 in total

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Authors:  Elisabeth Marchal; Ekaterina F Hult; Juan Huang; Stephen S Tobe
Journal:  BMC Res Notes       Date:  2013-06-19

3.  Capturing drug responses by quantitative promoter activity profiling.

Authors:  K Kajiyama; M Okada-Hatakeyama; Y Hayashizaki; H Kawaji; H Suzuki
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2013-09-25

4.  Identification of novel prognosis-related genes associated with cancer using integrative network analysis.

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Journal:  Sci Rep       Date:  2018-02-19       Impact factor: 4.379

  4 in total

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