Division of Gut Health, Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen, Scotland.
J Mol Diagn. 2011 Mar;13(2):233-42. doi: 10.1016/j.jmoldx.2010.10.001.
Colon cancers are characterized by aberrant gene expression signatures associated with disease initiation and progression. Identification of aberrant gene expression associated with colon carcinogenesis has increased significantly with application of gene array technologies. Downstream processing of these data has been hindered by the lack of robust multiplexed gene quantitative technologies facilitating study of the identified multiple gene targets. The GenomeLab Genetic Analysis System presents a novel technology platform for quantitative multiplexed gene expression analysis. This report describes the custom design of a GeXP multiplexed assay used to assess expression profiles of 14 inflammatory gene targets in normal, polyp, and tumor tissue. Characteristic normal, polyp, and tumor tissue gene expression profiles were obtained. Statistical analysis confirmed comparable relative quantitation of gene expression using the GeXP, macroarray, and single-plex real-time polymerase chain reaction assays. GeXP assays may be usefully applied in clinical and regulatory studies of multiple gene targets. This system permits custom-design options for relative quantification of multiple gene target expression, simultaneously in a single reaction, using nanogram quantities of total RNA template. The system provides an approach to advance the study of multiple targets identified from gene array analysis with potential for characterizing gene expression signatures in clinical diagnostics.
结肠癌的特征是与疾病发生和进展相关的异常基因表达特征。随着基因芯片技术的应用,与结肠癌发生相关的异常基因表达的鉴定显著增加。这些数据的下游处理受到缺乏稳健的多重基因定量技术的阻碍,这些技术有利于研究确定的多个基因靶点。基因组实验室遗传分析系统为定量多重基因表达分析提供了一种新颖的技术平台。本报告描述了用于评估正常、息肉和肿瘤组织中 14 个炎症基因靶标表达谱的 GeXP 多重分析的定制设计。获得了特征性的正常、息肉和肿瘤组织基因表达谱。统计分析证实,使用 GeXP、宏阵列和单重实时聚合酶链反应测定法,对基因表达进行可比的相对定量。GeXP 分析可用于多个基因靶点的临床和监管研究。该系统允许使用纳克数量的总 RNA 模板,在单个反应中同时对多个基因靶标表达进行相对定量的定制设计选项。该系统为从基因芯片分析中确定的多个靶点的研究提供了一种方法,具有在临床诊断中表征基因表达特征的潜力。