MicroRNA Expression Signatures in Barrett's Esophagus and Esophageal Adenocarcinoma

被引:109
作者
Yang, Hushan
Gu, Jian
Wang, Kenneth K. [4 ]
Zhang, Wei [2 ]
Xing, Jinliang [5 ,6 ]
Chen, Zhinan [5 ,6 ]
Ajani, Jaffer A. [3 ]
Wu, Xifeng [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Epidemiol, Unit 1340, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
[4] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN USA
[5] Fourth Mil Med Univ, Cell Engn Res Ctr, Xian 710032, Peoples R China
[6] Fourth Mil Med Univ, Dept Cell Biol, State Key Lab Canc Biol, Xian 710032, Peoples R China
关键词
HIGH-GRADE DYSPLASIA; GENE-EXPRESSION; FOLLOW-UP; CANCER; PROFILES; CARCINOMA; PATTERNS; PROGNOSIS; DIFFERENTIATION; SURVEILLANCE;
D O I
10.1158/1078-0432.CCR-09-0385
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Esophageal adenocarcinoma is a highly aggressive malignancy that frequently develops from Barrett's esophagus, a premalignant pathologic change occurring in the lower end of the esophagus. Identifying Barrett's esophagus patients at high risk of malignant transformation is essential to the prevention of esophageal adenocarcinoma. Although microRNA (miRNA) expression signatures have been associated with the etiology and prognosis of several types of cancers, their roles in the development of esophageal adenocarcinoma have not been extensively evaluated. Experimental Design: In this study, we analyzed the expression patterns of 470 human miRNAs using Agilent miRNA microarray in 32 disease/normal-paired tissues from 16 patients diagnosed with Barrett's esophagus of either low- or high-grade dysplasia, or esophageal adenocarcinoma. Results: Using unsupervised hierarchical clustering and class comparison analyses, we found that miRNA expression profiles in tissues of Barrett's esophagus with high-grade clysplasia were significantly different from their corresponding normal tissues. Similar findings were observed for esophageal adenocarcinoma, but not for Barrett's esophagus with low-grade clysplasia. The expression patterns of selected miRNAs were further validated using quantitative reverse transcription real-time PCR in an independent set of 75 pairs of disease/normal tissues. Finally, we identified several miRNAs that were involved in the progressions from low grade-dysplasia Barrett's esophagus to esophageal adenocarcinoma. Conclusions: We showed that miRNAs were involved in the development and progression of esophageal adenocarcinoma. The identified significant miRNAs that may become potential targets for early detection, chemoprevention, and treatment of esophageal cancer. (Clin Cancer Res 2009;15(18):5744-52)
引用
收藏
页码:5744 / 5752
页数:9
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