Identification of novel microRNA regulatory pathways associated with heterogeneous prostate cancer
Tang, Yifei1; Yan, Wenying1; Chen, Jiajia1; Luo, Cheng1,2; Kaipia, Antti3; Shen, Bairong1
刊名BMC SYSTEMS BIOLOGY
2013-10-16
卷号7
ISSN号1752-0509
DOI10.1186/1752-0509-7-S3-S6
文献子类Article; Proceedings Paper
英文摘要Background: MicroRNAs (miRNAs) are potential regulators that contribute to the pathogenesis of cancer. Microarray technologies have been widely used to characterize aberrant miRNA expression patterns in cancer. Nevertheless, the miRNAs expression signatures identified for a same cancer differs among laboratories due to the cancer heterogeneity. In addition, how the deregulated miRNAs coordinately contribute to the tumourigenic process of prostate cancer remains elusive. Results: We evaluated five outlier detection algorithms that take into account the heterogeneity of cancer samples. ORT was selected as the best method and applied to four prostate cancer associated microRNA expression datasets. After microRNA target prediction and pathway enrichment mapping, 38 Gene Ontology terms, 16 KEGG pathways and 99 GeneGO pathways are found putative prostate cancer associated. Comparison with our previous studies, we identified two putative novel pathways important in prostate cancer. The two novel pathways are 1) ligand-independent activation of ESR1 and ESR2 and 2) membrane-bound ESR1: interaction with growth factors signalling. Conclusions: We proved that expression signatures of at the pathway level well address the cancer heterogeneity and are more consistent than at the miRNA/gene levels. Based on this observation, we identified putative novel microRNA regulatory pathways which will help us to elucidate the cooperative function of different microRNAs in prostate cancer.
资助项目National Natural Science Foundation of China[91230117] ; National Natural Science Foundation of China[31170795] ; Specialized Research Fund for the Doctoral Program of Higher Education of China[20113201110015] ; International S&T Cooperation Program of Suzhou[SH201120] ; National High Technology Research and Development Program of China (863 program)[2012AA02A601]
WOS关键词DIFFERENTIAL GENE-EXPRESSION ; NEUROTROPHIN RECEPTOR P75(NTR) ; STEM-CELLS ; ACTIVIN-A ; GROWTH ; METASTASIS ; PREDICTION ; MIGRATION ; REVEALS ; KEGG
WOS研究方向Mathematical & Computational Biology
语种英语
出版者BIOMED CENTRAL LTD
WOS记录号WOS:000326808300006
内容类型期刊论文
源URL[http://119.78.100.183/handle/2S10ELR8/277419]  
专题药物发现与设计中心
通讯作者Shen, Bairong
作者单位1.Soochow Univ, Ctr Syst Biol, Suzhou 215006, Peoples R China;
2.Chinese Acad Sci, Shanghai Inst Mat Med, Drug Discovery & Design Ctr, Shanghai 200031, Peoples R China;
3.Tampere Univ Hosp, Dept Urol, Tamper 33521, Finland
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GB/T 7714
Tang, Yifei,Yan, Wenying,Chen, Jiajia,et al. Identification of novel microRNA regulatory pathways associated with heterogeneous prostate cancer[J]. BMC SYSTEMS BIOLOGY,2013,7.
APA Tang, Yifei,Yan, Wenying,Chen, Jiajia,Luo, Cheng,Kaipia, Antti,&Shen, Bairong.(2013).Identification of novel microRNA regulatory pathways associated with heterogeneous prostate cancer.BMC SYSTEMS BIOLOGY,7.
MLA Tang, Yifei,et al."Identification of novel microRNA regulatory pathways associated with heterogeneous prostate cancer".BMC SYSTEMS BIOLOGY 7(2013).
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