Prognostic microRNAs as biomarkers for prostate cancer

被引:1
|
作者
Palanisamy, Hema [1 ]
Manoharan, Jeevitha Priya [1 ]
Vidyalakshmi, Subramanian [1 ]
机构
[1] PSG Coll Technol, Dept Biotechnol, Coimbatore 641004, Tamil Nadu, India
关键词
Kaplan-Meier survival analysis; miRNA; mRNA; prostate cancer; protein-protein interaction network; TCGA; CELL-FREE; CONTACT INHIBITION; EXPRESSION; MIRNAS; METASTASIS; SIGNATURE; DIAGNOSIS;
D O I
10.4103/jcrt.jcrt_1469_22
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Prostate cancer is the second largest cancer, most commonly diagnosed in men. Several studies reveal that miRNAs (microRNAs) are involved in various stages of prostate cancer. miRNAs are a family of small non-coding RNA species that have been implicated in the post-transcriptional regulation of gene expression. The present in silico study aims at identifying miRNA biomarkers that are significantly associated with the regulation of genes involved in prostate cancer.<br /> Methods: Dataset of miRNA and mRNA of prostate adenocarcinoma patients and controls was downloaded from The Cancer Genome Atlas (TCGA), and differential gene expression analysis was carried out. ROC and Kaplan-Meier survival analyses were performed on differentially expressed miRNAs. Pathway analysis was carried out for significant miRNAs, and protein-protein interaction of involved genes and miRNAs was examined.<br /> Results: A total of 185 miRNAs were differentially expressed between the patients and the control. ROC and Kaplan-Meier survival analysis showed that the two miRNAs hsa-mir-133b and hsa-mir-17-5p were found to be significantly associated with prostate cancer prognosis. HAS2 and EPHA10 gene targets of identified miRNA were also differentially expressed. A protein-protein interaction (PPI) network was constructed, and the HAS2 gene was found to be interacting with the epidermal growth factor receptor (EGFR).<br /> Conclusion: This study highlights the potential of hsa-mir-133b and hsa-mir-17-5p miRNAs as biomarkers for the prognosis of prostate cancer. However, further experimental studies are required to validate this finding.
引用
收藏
页码:297 / 303
页数:7
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