Gene-gene interaction network analysis of ovarian cancer using TCGA data
Autor: | Jingru Shao, Qing Yang, Hongying Xu, Huanchun Ying, Jing Lv, Bin Yuan, Lili Wang, Tianshu Ying, Shanshan Jin |
---|---|
Rok vydání: | 2013 |
Předmět: |
Gene-gene interaction network
Functional modules Computer science Cell Cycle Pathway Microarray analysis techniques Research Function and pathway annotation DNA replication Obstetrics and Gynecology Computational biology Cell cycle medicine.disease Bioinformatics Metabolic pathway Oncology Obstetrics and Gynaecology Differentially expressed genes FOXM1 medicine Ovarian cancer Gene |
Zdroj: | Journal of Ovarian Research |
ISSN: | 1757-2215 |
DOI: | 10.1186/1757-2215-6-88 |
Popis: | Background: The Cancer Genome Atlas (TCGA) Data portal provides a platform for researchers to search, download, and analysis data generated by TCGA. The objective of this study was to explore the molecular mechanism of ovarian cancer pathogenesis. Methods: Microarray data of ovarian cancer were downloaded from TCGA database, and Limma package in R language was used to identify the differentially expressed genes (DEGs) between ovarian cancer and normal samples, followed by the function and pathway annotations of the DEGs. Next, NetBox software was used to for the gene-gene interaction (GGI) network construction and the corresponding modules identification, and functions of genes in the modules were screened using DAVID. Results: Our studies identified 332 DEGs, including 146 up-regulated genes which mainly involved in the cell cycle related functions and cell cycle pathway, and 186 down-regulated genes which were enriched in extracellular region par function, and Ether lipid metabolism pathway. GGI network was constructed by 127 DEGs and their significantly interacted 209 genes (LINKERs). In the top 10 nodes ranked by degrees in the network, 5 were LINKERs. Totally, 7 functional modules in the network were selected, and they were enriched in different functions and pathways, such as mitosis process, DNA replication and DNA double-strand synthesis, lipid synthesis processes and metabolic pathways. AR, BRCA1, TFDP1, FOXM1, CDK2, and DBF4 were identified as the transcript factors of the 7 modules. Conclusion: our data provides a comprehensive bioinformatics analysis of genes, functions, and pathways which may be involved in the pathogenesis of ovarian cancer. |
Databáze: | OpenAIRE |
Externí odkaz: |