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Revisiting miRNA Association with Melanoma Recurrence and Metastasis from a Machine Learning Point of View

The diagnostic and prognostic value of miRNAs in cutaneous melanoma (CM) has been broadly studied and supported by advanced bioinformatics tools. From early studies using miRNA arrays with several limitations, to the recent NGS-derived miRNA expression profiles, an accurate diagnostic panel of a com...

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Autores principales: Korfiati, Aigli, Grafanaki, Katerina, Kyriakopoulos, George C., Skeparnias, Ilias, Georgiou, Sophia, Sakellaropoulos, George, Stathopoulos, Constantinos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836065/
https://www.ncbi.nlm.nih.gov/pubmed/35163222
http://dx.doi.org/10.3390/ijms23031299
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author Korfiati, Aigli
Grafanaki, Katerina
Kyriakopoulos, George C.
Skeparnias, Ilias
Georgiou, Sophia
Sakellaropoulos, George
Stathopoulos, Constantinos
author_facet Korfiati, Aigli
Grafanaki, Katerina
Kyriakopoulos, George C.
Skeparnias, Ilias
Georgiou, Sophia
Sakellaropoulos, George
Stathopoulos, Constantinos
author_sort Korfiati, Aigli
collection PubMed
description The diagnostic and prognostic value of miRNAs in cutaneous melanoma (CM) has been broadly studied and supported by advanced bioinformatics tools. From early studies using miRNA arrays with several limitations, to the recent NGS-derived miRNA expression profiles, an accurate diagnostic panel of a comprehensive pre-specified set of miRNAs that could aid timely identification of specific cancer stages is still elusive, mainly because of the heterogeneity of the approaches and the samples. Herein, we summarize the existing studies that report several miRNAs as important diagnostic and prognostic biomarkers in CM. Using publicly available NGS data, we analyzed the correlation of specific miRNA expression profiles with the expression signatures of known gene targets. Combining network analytics with machine learning, we developed specific non-linear classification models that could successfully predict CM recurrence and metastasis, based on two newly identified miRNA signatures. Subsequent unbiased analyses and independent test sets (i.e., a dataset not used for training, as a validation cohort) using our prediction models resulted in 73.85% and 82.09% accuracy in predicting CM recurrence and metastasis, respectively. Overall, our approach combines detailed analysis of miRNA profiles with heuristic optimization and machine learning, which facilitates dimensionality reduction and optimization of the prediction models. Our approach provides an improved prediction strategy that could serve as an auxiliary tool towards precision treatment.
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spelling pubmed-88360652022-02-12 Revisiting miRNA Association with Melanoma Recurrence and Metastasis from a Machine Learning Point of View Korfiati, Aigli Grafanaki, Katerina Kyriakopoulos, George C. Skeparnias, Ilias Georgiou, Sophia Sakellaropoulos, George Stathopoulos, Constantinos Int J Mol Sci Review The diagnostic and prognostic value of miRNAs in cutaneous melanoma (CM) has been broadly studied and supported by advanced bioinformatics tools. From early studies using miRNA arrays with several limitations, to the recent NGS-derived miRNA expression profiles, an accurate diagnostic panel of a comprehensive pre-specified set of miRNAs that could aid timely identification of specific cancer stages is still elusive, mainly because of the heterogeneity of the approaches and the samples. Herein, we summarize the existing studies that report several miRNAs as important diagnostic and prognostic biomarkers in CM. Using publicly available NGS data, we analyzed the correlation of specific miRNA expression profiles with the expression signatures of known gene targets. Combining network analytics with machine learning, we developed specific non-linear classification models that could successfully predict CM recurrence and metastasis, based on two newly identified miRNA signatures. Subsequent unbiased analyses and independent test sets (i.e., a dataset not used for training, as a validation cohort) using our prediction models resulted in 73.85% and 82.09% accuracy in predicting CM recurrence and metastasis, respectively. Overall, our approach combines detailed analysis of miRNA profiles with heuristic optimization and machine learning, which facilitates dimensionality reduction and optimization of the prediction models. Our approach provides an improved prediction strategy that could serve as an auxiliary tool towards precision treatment. MDPI 2022-01-24 /pmc/articles/PMC8836065/ /pubmed/35163222 http://dx.doi.org/10.3390/ijms23031299 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Korfiati, Aigli
Grafanaki, Katerina
Kyriakopoulos, George C.
Skeparnias, Ilias
Georgiou, Sophia
Sakellaropoulos, George
Stathopoulos, Constantinos
Revisiting miRNA Association with Melanoma Recurrence and Metastasis from a Machine Learning Point of View
title Revisiting miRNA Association with Melanoma Recurrence and Metastasis from a Machine Learning Point of View
title_full Revisiting miRNA Association with Melanoma Recurrence and Metastasis from a Machine Learning Point of View
title_fullStr Revisiting miRNA Association with Melanoma Recurrence and Metastasis from a Machine Learning Point of View
title_full_unstemmed Revisiting miRNA Association with Melanoma Recurrence and Metastasis from a Machine Learning Point of View
title_short Revisiting miRNA Association with Melanoma Recurrence and Metastasis from a Machine Learning Point of View
title_sort revisiting mirna association with melanoma recurrence and metastasis from a machine learning point of view
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836065/
https://www.ncbi.nlm.nih.gov/pubmed/35163222
http://dx.doi.org/10.3390/ijms23031299
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