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PDE10A Inactivation Prevents Doxorubicin-Induced Cardiotoxicity and Tumor Growth.

Si ChenJiawei ChenWenting DuDeanne M MickelsenHangchuan ShiHan YuSparsh KumarChen Yan
Published in: Circulation research (2023)
Taken together, our study elucidates a novel role for PDE10A in cardiotoxicity induced by DOX and cancer growth. Given that PDE10A has been already proven to be a safe drug target, PDE10A inhibition may represent a novel therapeutic strategy in cancer therapy, with effects preventing DOX-induced cardiotoxicity and simultaneously antagonizing cancer growth.
Keyphrases
  • cancer therapy
  • papillary thyroid
  • high glucose
  • diabetic rats
  • drug delivery
  • drug induced
  • squamous cell
  • lymph node metastasis