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A prognostic nomogram integrating novel biomarkers identified by machine learning for cervical squamous cell carcinoma
BACKGROUND: Cervical cancer (CC) represents the fourth most frequently diagnosed malignancy affecting women all over the world. However, effective prognostic biomarkers are still limited for accurately identifying high-risk patients. Here, we provided a combination machine learning algorithm-based s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275455/ https://www.ncbi.nlm.nih.gov/pubmed/32503630 http://dx.doi.org/10.1186/s12967-020-02387-9 |
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author | Li, Yimin Lu, Shun Lan, Mei Peng, Xinhao Zhang, Zijian Lang, Jinyi |
author_facet | Li, Yimin Lu, Shun Lan, Mei Peng, Xinhao Zhang, Zijian Lang, Jinyi |
author_sort | Li, Yimin |
collection | PubMed |
description | BACKGROUND: Cervical cancer (CC) represents the fourth most frequently diagnosed malignancy affecting women all over the world. However, effective prognostic biomarkers are still limited for accurately identifying high-risk patients. Here, we provided a combination machine learning algorithm-based signature to predict the prognosis of cervical squamous cell carcinoma (CSCC). METHODS AND MATERIALS: After utilizing RNA sequencing (RNA-seq) data from 36 formalin-fixed and paraffin-embedded (FFPE) samples, the most significant modules were highlighted by the weighted gene co-expression network analysis (WGCNA). A candidate genes-based prognostic classifier was constructed by the least absolute shrinkage and selection operator (LASSO) and then validated in an independent validation set. Finally, based on the multivariate analysis, a nomogram including the FIGO stage, therapy outcome, and risk score level was built to predict progression-free survival (PFS) probability. RESULTS: A mRNA-based signature was developed to classify patients into high- and low-risk groups with significantly different PFS and overall survival (OS) rate (training set: p < 0.001 for PFS, p = 0.016 for OS; validation set: p = 0.002 for PFS, p = 0.028 for OS). The prognostic classifier was an independent and powerful prognostic biomarker for PFS in both cohorts (training set: hazard ratio [HR] = 0.13, 95% CI 0.05–0.33, p < 0.001; validation set: HR = 0.02, 95% CI 0.01–0.04, p < 0.001). A nomogram that integrated the independent prognostic factors was constructed for clinical application. The calibration curve showed that the nomogram was able to predict 1-, 3-, and 5-year PFS accurately, and it performed well in the external validation cohorts (concordance index: 0.828 and 0.864, respectively). CONCLUSION: The mRNA-based biomarker is a powerful and independent prognostic factor. Furthermore, the nomogram comprising our prognostic classifier is a promising predictor in identifying the progression risk of CSCC patients. |
format | Online Article Text |
id | pubmed-7275455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72754552020-06-08 A prognostic nomogram integrating novel biomarkers identified by machine learning for cervical squamous cell carcinoma Li, Yimin Lu, Shun Lan, Mei Peng, Xinhao Zhang, Zijian Lang, Jinyi J Transl Med Research BACKGROUND: Cervical cancer (CC) represents the fourth most frequently diagnosed malignancy affecting women all over the world. However, effective prognostic biomarkers are still limited for accurately identifying high-risk patients. Here, we provided a combination machine learning algorithm-based signature to predict the prognosis of cervical squamous cell carcinoma (CSCC). METHODS AND MATERIALS: After utilizing RNA sequencing (RNA-seq) data from 36 formalin-fixed and paraffin-embedded (FFPE) samples, the most significant modules were highlighted by the weighted gene co-expression network analysis (WGCNA). A candidate genes-based prognostic classifier was constructed by the least absolute shrinkage and selection operator (LASSO) and then validated in an independent validation set. Finally, based on the multivariate analysis, a nomogram including the FIGO stage, therapy outcome, and risk score level was built to predict progression-free survival (PFS) probability. RESULTS: A mRNA-based signature was developed to classify patients into high- and low-risk groups with significantly different PFS and overall survival (OS) rate (training set: p < 0.001 for PFS, p = 0.016 for OS; validation set: p = 0.002 for PFS, p = 0.028 for OS). The prognostic classifier was an independent and powerful prognostic biomarker for PFS in both cohorts (training set: hazard ratio [HR] = 0.13, 95% CI 0.05–0.33, p < 0.001; validation set: HR = 0.02, 95% CI 0.01–0.04, p < 0.001). A nomogram that integrated the independent prognostic factors was constructed for clinical application. The calibration curve showed that the nomogram was able to predict 1-, 3-, and 5-year PFS accurately, and it performed well in the external validation cohorts (concordance index: 0.828 and 0.864, respectively). CONCLUSION: The mRNA-based biomarker is a powerful and independent prognostic factor. Furthermore, the nomogram comprising our prognostic classifier is a promising predictor in identifying the progression risk of CSCC patients. BioMed Central 2020-06-05 /pmc/articles/PMC7275455/ /pubmed/32503630 http://dx.doi.org/10.1186/s12967-020-02387-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Li, Yimin Lu, Shun Lan, Mei Peng, Xinhao Zhang, Zijian Lang, Jinyi A prognostic nomogram integrating novel biomarkers identified by machine learning for cervical squamous cell carcinoma |
title | A prognostic nomogram integrating novel biomarkers identified by machine learning for cervical squamous cell carcinoma |
title_full | A prognostic nomogram integrating novel biomarkers identified by machine learning for cervical squamous cell carcinoma |
title_fullStr | A prognostic nomogram integrating novel biomarkers identified by machine learning for cervical squamous cell carcinoma |
title_full_unstemmed | A prognostic nomogram integrating novel biomarkers identified by machine learning for cervical squamous cell carcinoma |
title_short | A prognostic nomogram integrating novel biomarkers identified by machine learning for cervical squamous cell carcinoma |
title_sort | prognostic nomogram integrating novel biomarkers identified by machine learning for cervical squamous cell carcinoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275455/ https://www.ncbi.nlm.nih.gov/pubmed/32503630 http://dx.doi.org/10.1186/s12967-020-02387-9 |
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