Genome-wide expression profiling reveals novel biomarkers in epithelial ovarian cancer

被引:0
作者
Gautam, Priyanka [1 ]
Gupta, Sameer [2 ]
Sachan, Manisha [1 ]
机构
[1] Motilal Nehru Natl Inst Technol Allahabad, Dept Biotechnol, Prayagraj 211004, India
[2] King George Med Univ, Dept Surg Oncol, Lucknow, India
关键词
Bioinformatics analysis; Diagnostic biomarkers; Epithelial ovarian cancer; Gene expression; RNA-sequencing; QRT-PCR; Differentially expressed genes (DEGs); BREAST-CANCER; DNA-REPLICATION; GENE-EXPRESSION; MESSENGER-RNA; CYCLIN D1; BCL6; WNT2; FOXO; OVEREXPRESSION; ACTIVATION;
D O I
10.1016/j.prp.2023.154840
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Epithelial ovarian cancer (EOC) is the most aggressive and frequent malignancy detected among women worldwide. The pathophysiology of OC should, therefore be better understood to identify diagnostic, prognostic, and predictive novel biomarkers necessary for early detection, management, and prognostication. In this study, we aimed to investigate transcriptomic landscape and biomarker through RNA-seq data analysis. Further analysis by Protein Protein network identified top 10 Differentially Expressed Genes (DEGs). KEGG pathway enrichment analysis revealed the significant enrichment of DEGs in basal cell carcinoma, cell cycle and FoxO signalling pathway. The RNA-seq results of 10 DEGs were validated by QRT-PCR and TCGA database. Correlation studies were also performed between gene expression and clinical characteristics followed by survival analysis. Finally, 8 DEGs (CDKN1A, BCL6, CDC45, WNT2, TLR5, AQP5) including two novel DEGs (CSN1S1 and NKILA) were identified showing significant correlations with EOC characteristics. These may serve as interesting biomarkers and novel treatment targets and warrant further investigation into the functional outcome of EOC.
引用
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页数:12
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