Identifying the miRNA signature associated with survival time in patients with lung adenocarcinoma using miRNA expression profiles

被引:64
作者
Sathipati, Srinivasulu Yerukala [1 ]
Ho, Shinn-Ying [1 ,2 ]
机构
[1] Natl Chiao Tung Univ, Inst Bioinformat & Syst Biol, Hsinchu, Taiwan
[2] Natl Chiao Tung Univ, Dept Biol Sci & Technol, Hsinchu, Taiwan
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
SUPPORT VECTOR REGRESSION; MICRORNA EXPRESSION; TUMOR-SUPPRESSOR; CELL-PROLIFERATION; REDUCED EXPRESSION; MIR-152; FUNCTIONS; BREAST-CANCER; LET-7; APOPTOSIS; INVASION;
D O I
10.1038/s41598-017-07739-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lung adenocarcinoma is a multifactorial disease. MicroRNA (miRNA) expression profiles are extensively used for discovering potential theranostic biomarkers of lung cancer. This work proposes an optimized support vector regression (SVR) method called SVR-LUAD to simultaneously identify a set of miRNAs referred to the miRNA signature for estimating the survival time of lung adenocarcinoma patients using their miRNA expression profiles. SVR-LUAD uses an inheritable bi-objective combinatorial genetic algorithm to identify a small set of informative miRNAs cooperating with SVR by maximizing estimation accuracy. SVR-LUAD identified 18 out of 332 miRNAs using 10-fold cross-validation and achieved a correlation coefficient of 0.88 +/- 0.01 and mean absolute error of 0.56 +/- 0.03 year between real and estimated survival time. SVR-LUAD performs well compared to some well-recognized regression methods. The miRNA signature consists of the 18 miRNAs which strongly correlates with lung adenocarcinoma: hsa-let-7f-1, hsa-miR-16-1, hsa-miR-152, hsa-miR-217, hsa-miR-18a, hsa-miR- 193b, hsa-miR-3136, hsa-let-7g, hsa-miR-155, hsa-miR-3199-1, hsa-miR-219-2, hsa-miR-1254, hsa-miR-1291, hsa-miR-192, hsa-miR-3653, hsa-miR-3934, hsa-miR-342, and hsa-miR-141. Gene ontology annotation and pathway analysis of the miRNA signature revealed its biological significance in cancer and cellular pathways. This miRNA signature could aid in the development of novel therapeutic approaches to the treatment of lung adenocarcinoma.
引用
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页数:15
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