Identifying cancer-related microRNAs based on gene expression data

被引:73
|
作者
Zhao, Xing-Ming [1 ]
Liu, Ke-Qin [2 ,3 ]
Zhu, Guanghui [4 ]
He, Feng [1 ]
Duval, Beatrice [3 ]
Richer, Jean-Michel [3 ]
Huang, De-Shuang [1 ]
Jiang, Chang-Jun [1 ]
Hao, Jin-Kao [3 ]
Chen, Luonan [5 ]
机构
[1] Tongji Univ, Sch Elect & Informat Engn, Shanghai 201804, Peoples R China
[2] Wake Forest Sch Med, Ctr Bioinformat & Syst Biol, Dept Radiol, Winston Salem, NC 27157 USA
[3] Univ Angers, LERIA, F-49045 Angers 01, France
[4] Shanghai Univ, Dept Math, Shanghai 200444, Peoples R China
[5] Chinese Acad Sci, Shanghai Inst Biol Sci, Key Lab Syst Biol, Shanghai 200031, Peoples R China
基金
中国国家自然科学基金;
关键词
TUMOR-SUPPRESSOR; LUNG-CANCER; METASTASIS; PROFILES; PATHWAYS; GROWTH; IDENTIFICATION; PROGRESSION; SIGNATURES; MIR-137;
D O I
10.1093/bioinformatics/btu811
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: MicroRNAs (miRNAs) are short non-coding RNAs that play important roles in post-transcriptional regulations as well as other important biological processes. Recently, accumulating evidences indicate that miRNAs are extensively involved in cancer. However, it is a big challenge to identify which miRNAs are related to which cancer considering the complex processes involved in tumors, where one miRNA may target hundreds or even thousands of genes and one gene may regulate multiple miRNAs. Despite integrative analysis of matched gene and miRNA expression data can help identify cancer-associated miRNAs, such kind of data is not commonly available. On the other hand, there are huge amount of gene expression data that are publicly accessible. It will significantly improve the efficiency of characterizing miRNA's function in cancer if we can identify cancer miRNAs directly from gene expression data. Results: We present a novel computational framework to identify the cancer-related miRNAs based solely on gene expression profiles without requiring either miRNA expression data or the matched gene and miRNA expression data. The results on multiple cancer datasets show that our proposed method can effectively identify cancer-related miRNAs with higher precision compared with other popular approaches. Furthermore, some of our novel predictions are validated by both differentially expressed miRNAs and evidences from literature, implying the predictive power of our proposed method. In addition, we construct a cancer-miRNA-pathway network, which can help explain how miRNAs are involved in cancer.
引用
收藏
页码:1226 / 1234
页数:9
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