Why the study?
Doxorubicin is an effective chemotherapy limited by cardiotoxicity, prompting investigation into its underlying mechanisms.
Population
Five-week-old male mice and DOX-treated breast cancer patients
Comparison
Weekly DOX (4 mg/kg) vs saline injections
Design
Preclinical multi-omics study integrating transcriptomic and proteomic profiling with patient validation
Follow-up
4 days and 6 weeks post-DOX
Authors
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SERPINA3 merits evaluation as a translational biomarker for doxorubicin cardiotoxicity; leaves open validation and clinical utility in prospective human studies.
A multi-omics approach in a mouse model of doxorubicin-induced cardiotoxicity identified dynamic temporal changes in molecular pathways and highlighted SERPINA3 as a potential translational biomarker.
Dabour et al. (2025) studied this question.
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