INKing the Cardiotoxicity Out of Doxorubicin
- PMID: 37719425
- PMCID: PMC10504426
- DOI: 10.1016/j.jacbts.2023.05.001
INKing the Cardiotoxicity Out of Doxorubicin
Keywords: cardiomyopathy; doxorubicin; inflammatory; interferon-gamma; invariant natural killer T cells.
Conflict of interest statement
Dr Javaheri was supported by 1R01HL155344 from the National Heart, Lung, and Blood Institute and by the Children’s Discovery Institute of Washington University and St. Louis Children's Hospital (MC-FR-2020-919); supported by the Diabetes Research Center at Washington University in St. Louis of the National Institutes of Health under award number P30DK020579; supported by National Institutes of Health grant P30DK056341 (Nutrition Obesity Research Center); has a pending patent for fusion protein nanodiscs for the treatment of heart failure and eye disease, is a member of the scientific advisory board of Mobius Scientific, and has received research funding from AstraZeneca and Bitterroot Bio, unrelated to the studies in this paper. Dr Guo was supported by the American Heart Association Postdoctoral Fellowship (898679).
Comment on
- doi: 10.1016/j.jacbts.2023.02.014
References
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- Rawat P.S., Jaiswal A., Khurana A., Bhatti J.S., Navik U. Doxorubicin-induced cardiotoxicity: an update on the molecular mechanism and novel therapeutic strategies for effective management. Biomed Pharmacother. 2021;139 - PubMed
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- Obata Y., Ishimori N., Saito A., et al. Activation of invariant natural killer T cells by alpha-galactosylceramide ameliorates doxorubicin-induced cardiotoxicity in mice. Eur J Prev Cardiol. 2020;27:2358–2361. - PubMed
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