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Oxaliplatin-induced cardiotoxicity in mice is connected to the changes in energy metabolism in the heart tissue.

Junwei DuLeland C SudlowKiana ShahverdiHaiying ZhouMegan MichieThomas Hellmuth SchindlerJoshua D MitchellShamim MollahMikhail Y Berezin
Published in: bioRxiv : the preprint server for biology (2023)
This study uncovers the detrimental impact of chronic oxaliplatin treatment on heart metabolism in mice, linking high accumulative dosages to cardiotoxicity and heart damage. By identifying significant changes in gene expression related to energy metabolic pathways, the findings pave the way for the development of diagnostic methods to detect oxaliplatin-induced cardiotoxicity at an early stage. Furthermore, these insights may inform the creation of therapies that compensate for the energy deficit in the heart, ultimately preventing heart damage and improving patient outcomes in cancer treatment.
Keyphrases
  • heart failure
  • gene expression
  • early stage
  • atrial fibrillation
  • oxidative stress
  • drug induced
  • diabetic rats
  • type diabetes
  • dna methylation
  • squamous cell carcinoma
  • skeletal muscle
  • smoking cessation