心脏毒性
氧化应激
抗氧化剂
药理学
心力衰竭
药品
氧化还原
化疗
氧化磷酸化
医学
化学
生物信息学
生物
生物化学
内科学
有机化学
作者
Christian Cadeddu Dessalvi,Martino Deidda,Antonio Noto,Clelia Madeddu,Lucia Cugusi,Ciro Santoro,Teresa López‐Fernández,Maurizio Galderisi,Giuseppe Mercuro
标识
DOI:10.1089/ars.2020.8055
摘要
Significance: Chemotherapy-induced cardiotoxicity (CTX) has been associated with redox signaling imbalance. In fact, redox reactions are crucial for normal heart physiology, whereas excessive oxidative stress can cause cardiomyocyte structural damage. Recent Advances: An antioxidant approach as a cardioprotective strategy in this setting has shown encouraging results in preventing anticancer drug-induced CTX. Critical Issues: In fact, traditional heart failure drugs as well as many other compounds and nonpharmacological strategies, with a partial effect in reducing oxidative stress, have been shown to counterbalance chemotherapy-induced CTX in this setting to some extent. Future Directions: Given the various pathways of toxicity involved in different chemotherapeutic schemes, interactions with redox balance need to be fine-tuned and a personalized cardioprotective approach seems to be required.
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