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A novel miRNA-based classification model of risks and stages for clear cell renal cell carcinoma patients
BACKGROUND: Clear cell renal cell carcinoma (ccRCC) is the most common subtype of renal carcinoma and patients at advanced stage showed poor survival rate. Despite microRNAs (miRNAs) are used as potential biomarkers in many cancers, miRNA biomarkers for predicting the tumor stage of ccRCC are still...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8323484/ https://www.ncbi.nlm.nih.gov/pubmed/34058987 http://dx.doi.org/10.1186/s12859-021-04189-2 |
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author | Dessie, Eskezeia Y. Tsai, Jeffrey J. P. Chang, Jan-Gowth Ng, Ka-Lok |
author_facet | Dessie, Eskezeia Y. Tsai, Jeffrey J. P. Chang, Jan-Gowth Ng, Ka-Lok |
author_sort | Dessie, Eskezeia Y. |
collection | PubMed |
description | BACKGROUND: Clear cell renal cell carcinoma (ccRCC) is the most common subtype of renal carcinoma and patients at advanced stage showed poor survival rate. Despite microRNAs (miRNAs) are used as potential biomarkers in many cancers, miRNA biomarkers for predicting the tumor stage of ccRCC are still limitedly identified. Therefore, we proposed a new integrated machine learning (ML) strategy to identify a novel miRNA signature related to tumor stage and prognosis of ccRCC patients using miRNA expression profiles. A multivariate Cox regression model with three hybrid penalties including Least absolute shrinkage and selection operator (Lasso), Adaptive lasso and Elastic net algorithms was used to screen relevant prognostic related miRNAs. The best subset regression (BSR) model was used to identify optimal prognostic model. Five ML algorithms were used to develop stage classification models. The biological significance of the miRNA signature was analyzed by utilizing DIANA-mirPath. RESULTS: A four-miRNA signature associated with survival was identified and the expression of this signature was strongly correlated with high risk patients. The high risk patients had unfavorable overall survival compared with the low risk group (HR = 4.523, P-value = 2.86e−08). Univariate and multivariate analyses confirmed independent and translational value of this predictive model. A combined ML algorithm identified six miRNA signatures for cancer staging prediction. After using the data balancing algorithm SMOTE, the Support Vector Machine (SVM) algorithm achieved the best classification performance (accuracy = 0.923, sensitivity = 0.927, specificity = 0.919, MCC = 0.843) when compared with other classifiers. Furthermore, enrichment analysis indicated that the identified miRNA signature involved in cancer-associated pathways. CONCLUSIONS: A novel miRNA classification model using the identified prognostic and tumor stage associated miRNA signature will be useful for risk and stage stratification for clinical practice, and the identified miRNA signature can provide promising insight to understand the progression mechanism of ccRCC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04189-2. |
format | Online Article Text |
id | pubmed-8323484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83234842021-08-02 A novel miRNA-based classification model of risks and stages for clear cell renal cell carcinoma patients Dessie, Eskezeia Y. Tsai, Jeffrey J. P. Chang, Jan-Gowth Ng, Ka-Lok BMC Bioinformatics Methodology BACKGROUND: Clear cell renal cell carcinoma (ccRCC) is the most common subtype of renal carcinoma and patients at advanced stage showed poor survival rate. Despite microRNAs (miRNAs) are used as potential biomarkers in many cancers, miRNA biomarkers for predicting the tumor stage of ccRCC are still limitedly identified. Therefore, we proposed a new integrated machine learning (ML) strategy to identify a novel miRNA signature related to tumor stage and prognosis of ccRCC patients using miRNA expression profiles. A multivariate Cox regression model with three hybrid penalties including Least absolute shrinkage and selection operator (Lasso), Adaptive lasso and Elastic net algorithms was used to screen relevant prognostic related miRNAs. The best subset regression (BSR) model was used to identify optimal prognostic model. Five ML algorithms were used to develop stage classification models. The biological significance of the miRNA signature was analyzed by utilizing DIANA-mirPath. RESULTS: A four-miRNA signature associated with survival was identified and the expression of this signature was strongly correlated with high risk patients. The high risk patients had unfavorable overall survival compared with the low risk group (HR = 4.523, P-value = 2.86e−08). Univariate and multivariate analyses confirmed independent and translational value of this predictive model. A combined ML algorithm identified six miRNA signatures for cancer staging prediction. After using the data balancing algorithm SMOTE, the Support Vector Machine (SVM) algorithm achieved the best classification performance (accuracy = 0.923, sensitivity = 0.927, specificity = 0.919, MCC = 0.843) when compared with other classifiers. Furthermore, enrichment analysis indicated that the identified miRNA signature involved in cancer-associated pathways. CONCLUSIONS: A novel miRNA classification model using the identified prognostic and tumor stage associated miRNA signature will be useful for risk and stage stratification for clinical practice, and the identified miRNA signature can provide promising insight to understand the progression mechanism of ccRCC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04189-2. BioMed Central 2021-05-25 /pmc/articles/PMC8323484/ /pubmed/34058987 http://dx.doi.org/10.1186/s12859-021-04189-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 | Methodology Dessie, Eskezeia Y. Tsai, Jeffrey J. P. Chang, Jan-Gowth Ng, Ka-Lok A novel miRNA-based classification model of risks and stages for clear cell renal cell carcinoma patients |
title | A novel miRNA-based classification model of risks and stages for clear cell renal cell carcinoma patients |
title_full | A novel miRNA-based classification model of risks and stages for clear cell renal cell carcinoma patients |
title_fullStr | A novel miRNA-based classification model of risks and stages for clear cell renal cell carcinoma patients |
title_full_unstemmed | A novel miRNA-based classification model of risks and stages for clear cell renal cell carcinoma patients |
title_short | A novel miRNA-based classification model of risks and stages for clear cell renal cell carcinoma patients |
title_sort | novel mirna-based classification model of risks and stages for clear cell renal cell carcinoma patients |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8323484/ https://www.ncbi.nlm.nih.gov/pubmed/34058987 http://dx.doi.org/10.1186/s12859-021-04189-2 |
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