Smad3 promotes adverse cardiovascular remodeling and dysfunction in doxorubicin-treated hearts.

ABSTRACT: Many anticancer therapies cause serious cardiovascular complications that degrade quality of life and cause early mortality in treated patients. Specifically, doxorubicin is known as an effective anticancer agent that causes cardiomyopathy in treated patients. There has been growing interest in defining the role of endothelial cells in cardiac damage by doxorubicin. We have shown in the present study that endothelial nuclei accumulate more intravenously administered doxorubicin than other cardiac cell types. Doxorubicin enhanced cardiac production of the transforming growth factor-β (TGF-β) ligands and nuclear translocation of phospho-Smad3 in both cultured and in vivo cardiac endothelial cells. To examine the role of the TGF-β/mothers against decapentaplegic homolog 3 (Smad3) pathway in c

SUBMITTER: Cobb MS 

PROVIDER: S-EPMC9678413 | biostudies-literature | 2022 Dec

REPOSITORIES: biostudies-literature