Enhancing predictive modeling of drug resistance in type 1 breast cancer through dynamic bayesian networks and machine learning integration
The emergence of drug resistance in Type 1 (T1) breast cancer poses a critical challenge to effective treatment and patient outcomes. Our study introduces an innovative framework that integrates Bayesian statistical methods with machine learning (ML) to advance predictive modeling of drug resistance mechanisms in T1 breast cancer. By uniting the strengths of dynamic Bayesian networks (DBNs) and ML, this approach enables the analysis of complex, multi-dimensional clinical data, including genomic, proteomic, and treatment response datasets. DBNs are employed to model the temporal evolution of resistance mechanisms, capturing time-dependent biological changes. ML algorithms complement this by uncovering intricate patterns and forecasting resistance trajectories under various therapeutic regimens. This synergistic combination not only identifies key biomarkers and resistance pathways but also addresses uncertainty and variability in patient responses, providing a robust predictive tool. The resulting model offers actionable insights to clinicians, aiding in the optimization of treatment strategies and improving patient outcomes. This work highlights the transformative potential of integrating Bayesian and ML methodologies to unravel complex biological phenomena, paving the way for advancements in precision oncology and personalized medicine.
Authors
- Adillah Nurashikin Arshad (ORCID: https://orcid.org/0000-0003-1969-5992)
- Alessandro Nutini (ORCID: https://orcid.org/0000-0003-3263-7535)
- Muhammad Yousaf (ORCID: https://orcid.org/0000-0002-8094-5551)
Institutions
- IMT School for Advanced Studies Lucca (IT)
- COMSATS University Islamabad (PK)
Publication Details
- Journal
- International Journal of Computational Materials Science and Engineering
- Published
- 2025-01-10
- DOI
- https://doi.org/10.1142/s2047684125400020
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00