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A miRNAs Based Exploration of promising Biomarkers in Cervical Cancer using Bioinformatic Methods
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AbstractCervical Cancer (CC) is a gynecologic cancer. In this cancer early detection is incredibly tough because most of the patients are not have any specific symptoms that results in suspending the proper identification. In this work, we selected TCGA CESC datasets and miRNA Seq analysis was done. The expression profiles of miRNAs in cervical cancer datasets were investigated using bioinformatics tools. The expression profiles of miRNA in Normal tissue, primary tumor and metastatic samples were analyzed. Based on p-value, principal component analysis and comparative literature survey, we reported 6 over-expressed (5X) miRNA at metastatic stage namely, hsa-mir-363, hsa-mir-429, hsa-mir-141, hsa-mir-93, hsa-mir-203b and hsa-mir-18a. Expression profiles were compared in heatmap. The target genes for the selected miRNAs were investigated for interaction and pathway details. The identification of two hub proteins (PTEN and MYC) in Protein-Protein Interaction Network was followed by pathway analysis. Our results indicate thathsa-mir-363,hsa-mir-429, hsa-mir-141, hsa-mir-93, hsa-mir-203b and hsa-mir-18acould be a potential diagnostic biomarkers for early-stage CESC and serve as prognostic predictors for patients with CESC.
Cold Spring Harbor Laboratory
Title: A miRNAs Based Exploration of promising Biomarkers in Cervical Cancer using Bioinformatic Methods
Description:
AbstractCervical Cancer (CC) is a gynecologic cancer.
In this cancer early detection is incredibly tough because most of the patients are not have any specific symptoms that results in suspending the proper identification.
In this work, we selected TCGA CESC datasets and miRNA Seq analysis was done.
The expression profiles of miRNAs in cervical cancer datasets were investigated using bioinformatics tools.
The expression profiles of miRNA in Normal tissue, primary tumor and metastatic samples were analyzed.
Based on p-value, principal component analysis and comparative literature survey, we reported 6 over-expressed (5X) miRNA at metastatic stage namely, hsa-mir-363, hsa-mir-429, hsa-mir-141, hsa-mir-93, hsa-mir-203b and hsa-mir-18a.
Expression profiles were compared in heatmap.
The target genes for the selected miRNAs were investigated for interaction and pathway details.
The identification of two hub proteins (PTEN and MYC) in Protein-Protein Interaction Network was followed by pathway analysis.
Our results indicate thathsa-mir-363,hsa-mir-429, hsa-mir-141, hsa-mir-93, hsa-mir-203b and hsa-mir-18acould be a potential diagnostic biomarkers for early-stage CESC and serve as prognostic predictors for patients with CESC.
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