Identification of novel microRNA regulatory pathways associated with heterogeneous prostate cancer | |
Tang, Yifei1; Yan, Wenying1; Chen, Jiajia1; Luo, Cheng1,2![]() | |
刊名 | BMC SYSTEMS BIOLOGY
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2013-10-16 | |
卷号 | 7 |
ISSN号 | 1752-0509 |
DOI | 10.1186/1752-0509-7-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 |
推荐引用方式 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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