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

Journal

Publisher

MDPI
DOI: 10.3390/ijms23031299

Keywords

miRNAs; gene targets; cutaneous melanoma; artificial intelligence; metastasis; recurrence; NGS analysis; precision medicine

Funding

  1. INSPIRED-The National Research Infrastructures on Integrated Structural Biology, Drug Screening Efforts and Drug target functional characterization by the Operational Program Competitiveness, Entrepreneurship and Innovation (NSRF 2014-2020) [MIS 5002550]
  2. European Union (European Regional Development Fund)

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In this study, the diagnostic and prognostic value of miRNAs in cutaneous melanoma (CM) was investigated. Using advanced bioinformatics tools, the authors analyzed miRNA expression profiles and developed specific non-linear classification models to predict CM recurrence and metastasis. The results showed high accuracy in predicting CM outcomes, indicating the potential of miRNAs as diagnostic and prognostic biomarkers.
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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