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通过肿瘤转录组分析鉴定出的食管腺癌预后生物标志物。

Prognostic biomarkers for esophageal adenocarcinoma identified by analysis of tumor transcriptome.

机构信息

Department of Systems Biology, University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.

出版信息

PLoS One. 2010 Nov 30;5(11):e15074. doi: 10.1371/journal.pone.0015074.

DOI:10.1371/journal.pone.0015074
PMID:21152079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2994829/
Abstract

BACKGROUND

Despite many attempts to establish pre-treatment prognostic markers to understand the clinical biology of esophageal adenocarcinoma (EAC), validated clinical biomarkers or parameters remain elusive. We generated and analyzed tumor transcriptome to develop a practical biomarker prognostic signature in EAC.

METHODOLOGY/PRINCIPAL FINDINGS: Untreated esophageal endoscopic biopsy specimens were obtained from 64 patients undergoing surgery and chemoradiation. Using DNA microarray technology, genome-wide gene expression profiling was performed on 75 untreated cancer specimens from 64 EAC patients. By applying various statistical and informatical methods to gene expression data, we discovered distinct subgroups of EAC with differences in overall gene expression patterns and identified potential biomarkers significantly associated with prognosis. The candidate marker genes were further explored in formalin-fixed, paraffin-embedded tissues from an independent cohort (52 patients) using quantitative RT-PCR to measure gene expression. We identified two genes whose expression was associated with overall survival in 52 EAC patients and the combined 2-gene expression signature was independently associated with poor outcome (P<0.024) in the multivariate Cox hazard regression analysis.

CONCLUSIONS/SIGNIFICANCE: Our findings suggest that the molecular gene expression signatures are associated with prognosis of EAC patients and can be assessed prior to any therapy. This signature could provide important improvement for the management of EAC patients.

摘要

背景

尽管已经尝试了许多方法来建立治疗前的预后标志物,以了解食管腺癌(EAC)的临床生物学特性,但仍未找到经过验证的临床生物标志物或参数。我们生成并分析了肿瘤转录组,以开发用于 EAC 的实用生物标志物预后特征。

方法/主要发现:对 64 名接受手术和放化疗的患者进行内镜活检,获得未经治疗的食管内镜活检标本。对 64 名 EAC 患者的 75 个未经治疗的癌症标本进行了全基因组基因表达谱的 DNA 微阵列技术分析。通过对基因表达数据应用各种统计和信息学方法,我们发现了 EAC 的不同亚组,其总体基因表达模式存在差异,并确定了与预后显著相关的潜在生物标志物。使用定量 RT-PCR 在来自独立队列(52 名患者)的福尔马林固定、石蜡包埋组织中进一步探索候选标记基因,以测量基因表达。我们发现有两个基因的表达与 52 名 EAC 患者的总生存率相关,并且这两个基因的联合表达特征在多变量 Cox 风险回归分析中与不良预后独立相关(P<0.024)。

结论/意义:我们的研究结果表明,分子基因表达特征与 EAC 患者的预后相关,并且可以在任何治疗之前进行评估。该特征可以为 EAC 患者的管理提供重要的改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84c8/2994829/27a673e26681/pone.0015074.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84c8/2994829/5644e3b0a2a5/pone.0015074.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84c8/2994829/2e376683e5a3/pone.0015074.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84c8/2994829/765063d26553/pone.0015074.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84c8/2994829/27a673e26681/pone.0015074.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84c8/2994829/5644e3b0a2a5/pone.0015074.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84c8/2994829/2e376683e5a3/pone.0015074.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84c8/2994829/765063d26553/pone.0015074.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84c8/2994829/27a673e26681/pone.0015074.g004.jpg

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