Physiol Rep. 2026 Apr;14(8):e70877. doi: 10.14814/phy2.70877.
ABSTRACT
As a widely used anticancer drug for the treatment of chronic myeloid leukemia, ponatinib is known to cause severe cardiovascular toxicities. Cardiomyocytes are the major functional units in the myocardium, and impairment of their viability and function plays a crucial role in cardiotoxic responses. Previous studies have indicated direct toxicity of ponatinib on cardiomyocytes, but the effect of ponatinib on adult human primary cardiomyocytes (hPCMs) remains unknown, largely due to sample scarcity and the technical challenges associated with the adult human cardiomyocyte model. Based upon our previous work establishing hPCMs as a pharmacologically competent model, we tested the direct toxicity of ponatinib on these cells. We reveal suppression of AKT, but not ERK, phosphorylation upon ponatinib treatment. Treatment of hPCMs with AKT inhibitor MK-2206 phenocopied ponatinib, while restoration of AKT signaling with UCL-TRO-1938 or insulin partially rescued hPCMs from cell death, suggesting a potential protective effect.
PMID:41995108 | DOI:10.14814/phy2.70877