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CESCProg: a compact prognostic model and nomogram for cervical cancer based on miRNA biomarkers

Cervical squamous cell carcinoma, more commonly cervical cancer, is the fourth common cancer among women worldwide with substantial burden of disease, and less-invasive, reliable and effective methods for its prognosis are necessary today. Micro-RNAs are increasingly recognized as viable alternative...

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Autores principales: Muthamilselvan, Sangeetha, Palaniappan, Ashok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541812/
https://www.ncbi.nlm.nih.gov/pubmed/37786580
http://dx.doi.org/10.7717/peerj.15912
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author Muthamilselvan, Sangeetha
Palaniappan, Ashok
author_facet Muthamilselvan, Sangeetha
Palaniappan, Ashok
author_sort Muthamilselvan, Sangeetha
collection PubMed
description Cervical squamous cell carcinoma, more commonly cervical cancer, is the fourth common cancer among women worldwide with substantial burden of disease, and less-invasive, reliable and effective methods for its prognosis are necessary today. Micro-RNAs are increasingly recognized as viable alternative biomarkers for direct diagnosis and prognosis of disease conditions, including various cancers. In this work, we addressed the problem of systematically developing an miRNA-based nomogram for the reliable prognosis of cervical cancer. Towards this, we preprocessed public-domain miRNA -omics data from cervical cancer patients, and applied a cascade of filters in the following sequence: (i) differential expression criteria with respect to controls; (ii) significance with univariate survival analysis; (iii) passage through dimensionality reduction algorithms; and (iv) stepwise backward selection with multivariate Cox modeling. This workflow yielded a compact prognostic DEmiR signature of three miRNAs, namely hsa-miR-625-5p, hs-miR-95-3p, and hsa-miR-330-3p, which were used to construct a risk-score model for the classification of cervical cancer patients into high-risk and low-risk groups. The risk-score model was subjected to evaluation on an unseen test dataset, yielding a one-year AUROC of 0.84 and five-year AUROC of 0.71. The model was validated on an out-of-domain, external dataset yielding significantly worse prognosis for high-risk patients. The risk-score was combined with significant features of the clinical profile to establish a predictive prognostic nomogram. Both the miRNA-based risk score model and the integrated nomogram are freely available for academic and not-for-profit use at CESCProg, a web-app (https://apalania.shinyapps.io/cescprog).
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spelling pubmed-105418122023-10-02 CESCProg: a compact prognostic model and nomogram for cervical cancer based on miRNA biomarkers Muthamilselvan, Sangeetha Palaniappan, Ashok PeerJ Bioinformatics Cervical squamous cell carcinoma, more commonly cervical cancer, is the fourth common cancer among women worldwide with substantial burden of disease, and less-invasive, reliable and effective methods for its prognosis are necessary today. Micro-RNAs are increasingly recognized as viable alternative biomarkers for direct diagnosis and prognosis of disease conditions, including various cancers. In this work, we addressed the problem of systematically developing an miRNA-based nomogram for the reliable prognosis of cervical cancer. Towards this, we preprocessed public-domain miRNA -omics data from cervical cancer patients, and applied a cascade of filters in the following sequence: (i) differential expression criteria with respect to controls; (ii) significance with univariate survival analysis; (iii) passage through dimensionality reduction algorithms; and (iv) stepwise backward selection with multivariate Cox modeling. This workflow yielded a compact prognostic DEmiR signature of three miRNAs, namely hsa-miR-625-5p, hs-miR-95-3p, and hsa-miR-330-3p, which were used to construct a risk-score model for the classification of cervical cancer patients into high-risk and low-risk groups. The risk-score model was subjected to evaluation on an unseen test dataset, yielding a one-year AUROC of 0.84 and five-year AUROC of 0.71. The model was validated on an out-of-domain, external dataset yielding significantly worse prognosis for high-risk patients. The risk-score was combined with significant features of the clinical profile to establish a predictive prognostic nomogram. Both the miRNA-based risk score model and the integrated nomogram are freely available for academic and not-for-profit use at CESCProg, a web-app (https://apalania.shinyapps.io/cescprog). PeerJ Inc. 2023-09-27 /pmc/articles/PMC10541812/ /pubmed/37786580 http://dx.doi.org/10.7717/peerj.15912 Text en ©2023 Muthamilselvan et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Bioinformatics
Muthamilselvan, Sangeetha
Palaniappan, Ashok
CESCProg: a compact prognostic model and nomogram for cervical cancer based on miRNA biomarkers
title CESCProg: a compact prognostic model and nomogram for cervical cancer based on miRNA biomarkers
title_full CESCProg: a compact prognostic model and nomogram for cervical cancer based on miRNA biomarkers
title_fullStr CESCProg: a compact prognostic model and nomogram for cervical cancer based on miRNA biomarkers
title_full_unstemmed CESCProg: a compact prognostic model and nomogram for cervical cancer based on miRNA biomarkers
title_short CESCProg: a compact prognostic model and nomogram for cervical cancer based on miRNA biomarkers
title_sort cescprog: a compact prognostic model and nomogram for cervical cancer based on mirna biomarkers
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541812/
https://www.ncbi.nlm.nih.gov/pubmed/37786580
http://dx.doi.org/10.7717/peerj.15912
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