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本文引用的文献

1
The inflammatory microenvironment in colorectal neoplasia.结直肠肿瘤中的炎症微环境。
PLoS One. 2011 Jan 7;6(1):e15366. doi: 10.1371/journal.pone.0015366.
2
Gamma-oryzanol rich fraction regulates the expression of antioxidant and oxidative stress related genes in stressed rat's liver.富含γ-谷维素的馏分调节应激大鼠肝脏中抗氧化和氧化应激相关基因的表达。
Nutr Metab (Lond). 2010 Mar 24;7:23. doi: 10.1186/1743-7075-7-23.
3
Realtime PCR is more sensitive than multiplex PCR for diagnosis and serotyping in children with culture negative pneumococcal invasive disease.实时 PCR 比多重 PCR 更敏感,可用于诊断和血清分型儿童中培养阴性的肺炎球菌侵袭性疾病。
PLoS One. 2010 Feb 19;5(2):e9282. doi: 10.1371/journal.pone.0009282.
4
Differential expression of the chemokines GRO-2, GRO-3, and interleukin-8 in colon cancer and their impact on metastatic disease and survival.趋化因子 GRO-2、GRO-3 和白细胞介素-8 在结肠癌中的差异表达及其对转移疾病和生存的影响。
Int J Colorectal Dis. 2010 May;25(5):573-81. doi: 10.1007/s00384-010-0901-1. Epub 2010 Feb 17.
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Why the need for qPCR publication guidelines?--The case for MIQE.为什么需要 qPCR 发表指南?--MIQE 的案例。
Methods. 2010 Apr;50(4):217-26. doi: 10.1016/j.ymeth.2009.12.006. Epub 2009 Dec 16.
6
Reliability of real-time reverse-transcription PCR in clinical diagnostics: gold standard or substandard?实时逆转录PCR在临床诊断中的可靠性:金标准还是不合格标准?
Expert Rev Mol Diagn. 2009 Mar;9(2):187-97. doi: 10.1586/14737159.9.2.187.
7
Analytical validation of the GeXP analyzer and design of a workflow for cancer-biomarker discovery using multiplexed gene-expression profiling.GeXP分析仪的分析验证及使用多重基因表达谱进行癌症生物标志物发现的工作流程设计。
Anal Bioanal Chem. 2009 Mar;393(5):1505-11. doi: 10.1007/s00216-008-2436-7. Epub 2008 Oct 29.
8
Influence of interleukin-8 and interleukin-10 on sporadic colon cancer development and progression.白细胞介素-8和白细胞介素-10对散发性结肠癌发生发展的影响。
Carcinogenesis. 2008 Aug;29(8):1572-80. doi: 10.1093/carcin/bgn164. Epub 2008 Jul 14.
9
Cross-platform comparison of SYBR Green real-time PCR with TaqMan PCR, microarrays and other gene expression measurement technologies evaluated in the MicroArray Quality Control (MAQC) study.在微阵列质量控制(MAQC)研究中对SYBR Green实时荧光定量PCR与TaqMan PCR、微阵列及其他基因表达测量技术进行的跨平台比较。
BMC Genomics. 2008 Jul 11;9:328. doi: 10.1186/1471-2164-9-328.
10
Screening and surveillance colonoscopy in chronic Crohn's colitis: results of a surveillance program spanning 25 years.慢性克罗恩病性结肠炎的筛查及监测性结肠镜检查:一项长达25年监测项目的结果
Clin Gastroenterol Hepatol. 2008 Sep;6(9):993-8; quiz 953-4. doi: 10.1016/j.cgh.2008.03.019. Epub 2008 Jun 27.

用于评估正常结肠、息肉和肿瘤组织中炎症基因靶标表达谱的 GeXP 多重分析的定制设计。

Custom design of a GeXP multiplexed assay used to assess expression profiles of inflammatory gene targets in normal colon, polyp, and tumor tissue.

机构信息

Division of Gut Health, Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen, Scotland.

出版信息

J Mol Diagn. 2011 Mar;13(2):233-42. doi: 10.1016/j.jmoldx.2010.10.001.

DOI:10.1016/j.jmoldx.2010.10.001
PMID:21354059
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3128578/
Abstract

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.

摘要

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。