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Identification of Key Genes and Pathways in Cervical Cancer by Bioinformatics Analysis
Xuan Wu1,2, Li Peng3, Yaqin Zhang1,2
1Key Laboratory of Carcinogenesis of the Chinese Ministry of Health and the Key Laboratory of Carcinogenesis and Cancer Invasion of Chinese Ministry of Education, Xiangya Hospital, Central South University, Changsha 410078, P.R. China.
Abstract:
Cervical cancer is a common malignant tumour of the female reproductive system that seriously threatens the health of women. The aims of this study were to identify key genes and pathways and to illuminate new molecular mechanisms underlying cervical cancer. Altogether, 1829 DEGs were identified, including 794 significantly down-regulated DEGs and 1035 significantly up-regulated DEGs. GO analysis suggested that the up-regulated DEGs were mainly enriched in mitotic cell cycle processes, including DNA replication, organelle fission, chromosome segregation and cell cycle phase transition, and that the down-regulated DEGs were primarily enriched in development and differentiation processes, such as tissue development, epidermis development, skin development, keratinocyte differentiation, epidermal cell differentiation and epithelial cell differentiation. KEGG pathway analysis showed that the DEGs were significantly enriched in cell cycle, DNA replication, the p53 signalling pathway, pathways in cancer and oocyte meiosis. The top 9 hub genes with a high degree of connectivity (over 72 in the PPI network) were down-regulated TSPO, CCND1, and FOS and up-regulated CDK1, TOP2A, CCNB1, PCNA, BIRC5 and MAD2L1. Module analysis indicated that the top 3 modules were significantly enriched in mitotic cell cycle, DNA replication and regulation of cell cycle (P < 0.01). The heat map based on TCGA database preliminarily demonstrated the expression change of the key genes in cervical cancer. GSEA results were basically coincident with the front enrichment analysis results. By comprehensive analysis, we confirmed that cell cycle was a key biological process and a critical driver in cervical cancer. In conclusion, this study identified DEGs and screened the key genes and pathways closely related to cervical cancer by bioinformatics analysis, simultaneously deepening our understanding of the molecular mechanisms underlying the occurrence and progression of cervical cancer. These results might hold promise for finding potential therapeutic targets of cervical cancer.
Insights
This study identifies key genes and pathways in cervical cancer, revealing that the cell cycle is a critical driver of this disease. Findings may lead to new therapeutic targets for cervical cancer treatment.
Area of Science:
- Oncology
- Genomics
- Bioinformatics
Background:
- Cervical cancer poses a significant global health threat to women's reproductive health.
- Understanding the molecular mechanisms of cervical cancer is crucial for developing effective treatments.
Purpose of the Study:
- To identify key genes and molecular pathways involved in cervical cancer.
- To elucidate novel molecular mechanisms underlying cervical cancer development and progression.
Main Methods:
- Differential gene expression (DEG) analysis was performed on cervical cancer data.
- Gene Ontology (GO) and KEGG pathway analyses were conducted.
- Protein-protein interaction (PPI) network and module analyses were utilized.
- Gene Set Enrichment Analysis (GSEA) and TCGA database were employed.
Main Results:
- 1829 differentially expressed genes (DEGs) were identified (794 down-regulated, 1035 up-regulated).
- Up-regulated DEGs were enriched in cell cycle and DNA replication; down-regulated DEGs in differentiation processes.
- Key pathways identified include cell cycle, DNA replication, and the p53 signaling pathway.
- Nine hub genes (e.g., CDK1, TOP2A, CCNB1, PCNA, BIRC5, MAD2L1, TSPO, CCND1, FOS) were highlighted.
- The cell cycle was confirmed as a critical biological process and driver in cervical cancer.
Conclusions:
- Bioinformatic analysis identified key genes and pathways crucial for cervical cancer.
- The cell cycle is a central mechanism in the occurrence and progression of cervical cancer.
- These findings offer potential therapeutic targets for cervical cancer intervention.
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