A four-gene signature associated with clinical features can better predict prognosis in prostate cancer.
Penghui YuanLe LingQing FanXintao GaoTaotao SunJianping MiaoXianglin YuanJihong LiuZhihua WangPublished in: Cancer medicine (2020)
Prostate cancer (PCa) is one of the most deadly urinary tumors in men globally, and the 5-year over survival is poor due to metastasis of tumor. It is significant to explore potential biomarkers for early diagnosis and personalized therapy of PCa. In the present study, we performed an integrated analysis based on multiple microarrays in the Gene Expression Omnibus (GEO) dataset and obtained differentially expressed genes (DEGs) between 510 PCa and 259 benign issues. The weighted correlation network analysis indicated that prognostic profile was the most relevant to DEGs. Then, univariate and multivariate COX regression analyses were conducted and four prognostic genes were obtained to establish a four-gene prognostic model. And the predictive effect and expression profiles of the four genes were well validated in another GEO dataset, The Cancer Genome Atlas and the Human Protein Atlas datasets. Furthermore, combination of four-gene model and clinical features was analyzed systematically to guide the prognosis of patients with PCa to a largest extent. In summary, our findings indicate that four genes had important prognostic significance in PCa and combination of four-gene model and clinical features could achieve a better prediction to guide the prognosis of patients with PCa.
Keyphrases
- genome wide
- genome wide identification
- prostate cancer
- dna methylation
- genome wide analysis
- copy number
- network analysis
- gene expression
- transcription factor
- bioinformatics analysis
- radical prostatectomy
- single cell
- small molecule
- squamous cell carcinoma
- magnetic resonance imaging
- papillary thyroid
- young adults
- bone marrow
- middle aged
- protein protein