Using Proteomics Data to Identify Personalized Treatments in Multiple Myeloma: A Machine Learning Approach.

Autor: Katsenou A; Department of Electronics and Electrical Engineering, Trinity College Dublin, D02 PN40 Dublin, Ireland.; School of Computer Science, University of Bristol, Bristol BS1 8UB, UK., O'Farrell R; Department of Electronics and Electrical Engineering, Trinity College Dublin, D02 PN40 Dublin, Ireland., Dowling P; Department of Biology, Maynooth University, W23 F2K8 Kildare, Ireland., Heckman CA; Institute for Molecular Medicine Finland-FIMM, HiLIFE-Helsinki Institute of Life Science, iCAN Digital Precision Cancer Medicine Flagship, University of Helsinki, 00290 Helsinki, Finland., O'Gorman P; Department of Haematology, Mater Misericordiae University Hospital, D07 R2WY Dublin, Ireland., Bazou D; School of Medicine, University College Dublin, D04 V1W8 Dublin, Ireland.
Jazyk: angličtina
Zdroj: International journal of molecular sciences [Int J Mol Sci] 2023 Oct 25; Vol. 24 (21). Date of Electronic Publication: 2023 Oct 25.
DOI: 10.3390/ijms242115570
Abstrakt: This paper describes a machine learning (ML) decision support system to provide a list of chemotherapeutics that individual multiple myeloma (MM) patients are sensitive/resistant to, based on their proteomic profile. The methodology used in this study involved understanding the parameter space and selecting the dominant features (proteomics data), identifying patterns of proteomic profiles and their association to the recommended treatments, and defining the decision support system of personalized treatment as a classification problem. During the data analysis, we compared several ML algorithms, such as linear regression, Random Forest, and support vector machines, to classify patients as sensitive/resistant to therapeutics. A further analysis examined data-balancing techniques that emerged due to the small cohort size. The results suggest that utilizing proteomics data is a promising approach for identifying effective treatment options for patients with MM (reaching on average an accuracy of 81%). Although this pilot study was limited by the small patient cohort (39 patients), which restricted the training and validation of the explored ML solutions to identify complex associations between proteins, it holds great promise for developing personalized anti-MM treatments using ML approaches.
Databáze: MEDLINE
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