| Literature DB >> 31768571 |
Luciana L Ferreira1, Marlene Cervantes2, Hugo J C Froufe3, Conceição Egas1,3, Teresa Cunha-Oliveira1, Paolo Sassone-Corsi2, Paulo J Oliveira4,5.
Abstract
Circadian rhythms disruption can be the cause of chronic diseases. External cues, including therapeutic drugs, have been shown to modulate peripheral-circadian clocks. Since anthracycline cardiotoxicity is associated with loss of mitochondrial function and metabolic remodeling, we investigated whether the energetic failure induced by sub-chronic doxorubicin (DOX) treatment in juvenile mice was associated with persistent disruption of circadian regulators. Juvenile C57BL/6J male mice were subjected to a sub-chronic DOX treatment (4 weekly injections of 5 mg/kg DOX) and several cardiac parameters, as well as circadian-gene expression and acetylation patterns, were analyzed after 6 weeks of recovery time. Complementary experiments were performed with Mouse Embryonic Fibroblasts (MEFs) and Human Embryonic Kidney 293 cells. DOX-treated juvenile mice showed cardiotoxicity markers and persistent alterations of transcriptional- and signaling cardiac circadian homeostasis. The results showed a delayed influence of DOX on gene expression, accompanied by changes in SIRT1-mediated cyclic deacetylation. The mechanism behind DOX interference with the circadian clock was further studied in vitro, in which were observed alterations of circadian-gene expression and increased BMAL1 SIRT1-mediated deacetylation. In conclusion, DOX treatment in juvenile mice resulted in disruption of oscillatory molecular mechanisms including gene expression and acetylation profiles.Entities:
Keywords: Cardiotoxicity; Chemotherapy; Circadian clock; Doxorubicin; Mitochondria; Protein acetylation
Year: 2019 PMID: 31768571 DOI: 10.1007/s00204-019-02626-z
Source DB: PubMed Journal: Arch Toxicol ISSN: 0340-5761 Impact factor: 5.153