Journal
CARDIOVASCULAR TOXICOLOGY
Volume 20, Issue 3, Pages 312-320Publisher
HUMANA PRESS INC
DOI: 10.1007/s12012-019-09554-5
Keywords
Dexrazoxane; Doxorubicin; Cardiac myocytes; Topoisomerase II beta; Bortezomib; Cardiotoxicity; Proteasome
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Funding
- CIHR [MOP13748] Funding Source: Medline
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Dexrazoxane is clinically used to reduce doxorubicin cardiotoxicity and anthracycline-induced extravasation injury. Dexrazoxane is a strong catalytic inhibitor of topoisomerase II. It can also undergo metabolism to form an iron-binding analog of EDTA. Dexrazoxane was originally thought to act by reducing iron-dependent doxorubicin-based oxidative stress. However, a competing hypothesis posits that dexrazoxane may be protective through its ability to inhibit and reduce topoisomerase II beta protein levels in the heart. A primary neonatal rat myocyte model was used to study the mechanism by which dexrazoxane protects against doxorubicin-induced myocyte damage. This study characterized the kinetics of the rapid and nearly complete dexrazoxane-induced loss of topoisomerase II beta protein from neonatal rat cardiac myocytes. Immunofluorescent staining of attached myocytes for topoisomerase II beta revealed that most of the topoisomerase II beta was localized to the nucleus, although it was also present in the cytoplasm. Dexrazoxane treatment resulted in an almost complete reduction of topoisomerase II beta in the nucleus and a lesser reduction in the cytoplasm. The recovery of topoisomerase II beta levels after a pulse topoisomerase II beta inhibitory concentration of dexrazoxane occurred slowly, with partial recovery only occurring after 24 h. The ability of dexrazoxane to reduce doxorubicin-induced damage to myocytes was greatest when topoisomerase II beta levels were at their lowest.
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