Prognostic value of the tumor‐specific ceRNA network in epithelial ovarian cancer. Issue 12 (31st May 2019)
- Record Type:
- Journal Article
- Title:
- Prognostic value of the tumor‐specific ceRNA network in epithelial ovarian cancer. Issue 12 (31st May 2019)
- Main Title:
- Prognostic value of the tumor‐specific ceRNA network in epithelial ovarian cancer
- Authors:
- Li, Gailing
Han, Liping
Ren, Fang
Zhang, Ruitao
Qin, Guijun - Abstract:
- Abstract: Epithelial ovarian cancer is one of the leading causes of cancer‐related death worldwide. Growing evidence indicates that multiple complex altered pathways play important regulatory roles in the development and progression of a variety of cancers, including epithelial ovarian cancer. However, the underlying mechanisms remain unclear. First, we identified differentially expressed messenger RNAs (mRNAs), long noncoding RNAs (lncRNAs), and microRNAs (miRNAs) in epithelial ovarian cancer by comparing the expression profiles between epithelial ovarian cancer samples and normal tissue samples in different GEO datasets. Then, GO‐ and KEGG‐pathway‐enrichment analyses were applied to investigate the primary functions of the overlapped differentially expressed mRNAs. Moreover, the primary enriched genes were used to construct the signal‐network with Cytoscape software. In addition, we integrated the relationship among lncRNAs‐miRNAs‐mRNAs to create a competing endogenous RNA network. Finally, mRNAs that were associated with patient prognosis in epithelial ovarian cancer were selected using univariate Cox regression analysis. A total of 2, 225 mRNAs, 336 lncRNAs, and 14 miRNAs were shown to be differentially expressed in epithelial ovarian cancer compared with normal tissues. The dysregulated mRNAs were primarily enriched in cell division and signal transduction, according to Gene Ontology, whereas, according to KEGG, they were primarily enriched in metabolic pathways andAbstract: Epithelial ovarian cancer is one of the leading causes of cancer‐related death worldwide. Growing evidence indicates that multiple complex altered pathways play important regulatory roles in the development and progression of a variety of cancers, including epithelial ovarian cancer. However, the underlying mechanisms remain unclear. First, we identified differentially expressed messenger RNAs (mRNAs), long noncoding RNAs (lncRNAs), and microRNAs (miRNAs) in epithelial ovarian cancer by comparing the expression profiles between epithelial ovarian cancer samples and normal tissue samples in different GEO datasets. Then, GO‐ and KEGG‐pathway‐enrichment analyses were applied to investigate the primary functions of the overlapped differentially expressed mRNAs. Moreover, the primary enriched genes were used to construct the signal‐network with Cytoscape software. In addition, we integrated the relationship among lncRNAs‐miRNAs‐mRNAs to create a competing endogenous RNA network. Finally, mRNAs that were associated with patient prognosis in epithelial ovarian cancer were selected using univariate Cox regression analysis. A total of 2, 225 mRNAs, 336 lncRNAs, and 14 miRNAs were shown to be differentially expressed in epithelial ovarian cancer compared with normal tissues. The dysregulated mRNAs were primarily enriched in cell division and signal transduction, according to Gene Ontology, whereas, according to KEGG, they were primarily enriched in metabolic pathways and pathways in cancer. A total of 10 mRNAs were associated with patient prognosis in ovarian cancer. This study identifies a novel lncRNA–miRNA–mRNA network, which may suggest potential molecular mechanisms underlying the development of epithelial ovarian cancer, providing new insights for survival prediction and interventional strategies for epithelial ovarian cancer. Abstract : This study identifies a novel lncRNA–miRNA–mRNA network, which may suggest potential molecular mechanisms underlying the development of epithelial ovarian cancer, providing new insights for survival prediction and interventional strategies for epithelial ovarian cancer. … (more)
- Is Part Of:
- Journal of cellular physiology. Volume 234:Issue 12(2019:Dec.)
- Journal:
- Journal of cellular physiology
- Issue:
- Volume 234:Issue 12(2019:Dec.)
- Issue Display:
- Volume 234, Issue 12 (2019)
- Year:
- 2019
- Volume:
- 234
- Issue:
- 12
- Issue Sort Value:
- 2019-0234-0012-0000
- Page Start:
- 22071
- Page End:
- 22081
- Publication Date:
- 2019-05-31
- Subjects:
- biomarkers -- EOC -- lncRNAs -- miRNAs
Physiology -- Periodicals
Cell physiology -- Periodicals
571.6 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4652 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcp.28770 ↗
- Languages:
- English
- ISSNs:
- 0021-9541
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.020000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26741.xml