MicroRNA profiling and prediction of recurrence/relapse-free survival in stage I lung cancer

被引:114
|
作者
Lu, Yan [4 ]
Govindan, Ramaswamy [5 ]
Wang, Liang [6 ]
Liu, Peng-yuan [3 ,4 ]
Goodgame, Boone [5 ]
Wen, Weidong [1 ]
Sezhiyan, Ananth [5 ]
Pfeifer, John [5 ]
Li, Ya-fei [6 ]
Hua, Xing [3 ,4 ]
Wang, Yian [1 ]
Yang, Ping [6 ]
You, Ming [1 ,2 ,3 ]
机构
[1] Washington Univ, Dept Surg, St Louis, MO 63110 USA
[2] Med Coll Wisconsin, Dept Pharmacol & Toxicol, Milwaukee, WI 53226 USA
[3] Med Coll Wisconsin, Ctr Canc, Milwaukee, WI 53226 USA
[4] Med Coll Wisconsin, Dept Physiol, Milwaukee, WI 53226 USA
[5] Washington Univ, Alvin J Siteman Canc Ctr, St Louis, MO 63110 USA
[6] Mayo Clin, Dept Hlth Sci Res, Rochester, MN 55905 USA
基金
美国国家卫生研究院;
关键词
SQUAMOUS-CELL CARCINOMA; GENE-EXPRESSION; ADENOCARCINOMA; SIGNATURES; PROGNOSIS; P53; PROLIFERATION; CLASSIFIERS; METASTASIS; GROWTH;
D O I
10.1093/carcin/bgs100
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
About 30% stage I non-small cell lung cancer (NSCLC) patients undergoing resection will recur. Robust prognostic markers are required to better manage therapy options. MicroRNAs (miRNAs) are a class of small non-coding RNAs of 19-25 nt and play important roles in gene regulation in human cancers. The purpose of this study is to identify miRNA expression profiles that would better predict prognosis of stage I NSCLC. MiRNAs extracted from 527 stage I NSCLC patients were profiled on the human miRNA expression profiling v2 panel (Illumina). The expression profiles were analyzed for their association with cancer subtypes, lung cancer brain metastasis and recurrence/relapse free survival (RFS). MiRNA expression patterns between lung adenocarcinoma and squamous cell carcinoma differed significantly with 171 miRNAs, including Let-7 family members and miR-205. Ten miRNAs associated with brain metastasis were identified including miR-145*, which inhibit cell invasion and metastasis. Two miRNA signatures that are highly predictive of RFS were identified. The first contained 34 miRNAs derived from 357 stage I NSCLC patients independent of cancer subtype, whereas the second containing 27 miRNAs was adenocarcinoma specific. Both signatures were validated using formalin-fixed paraffin embedded and/or fresh frozen tissues in independent data set with 170 stage I patients. Our findings have important prognostic or therapeutic implications for the management of stage I lung cancer patients. The identified miRNAs hold great potential as targets for histology-specific treatment or prevention and treatment of recurrent disease.
引用
收藏
页码:1046 / 1054
页数:9
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