Department of Cardiology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
Int J Mol Sci. 2024 Sep 22;25(18):10177. doi: 10.3390/ijms251810177.
Certain anticancer therapies inevitably increase the risk of cardiovascular events, now the second leading cause of death among cancer patients. This underscores the critical need for developing effective drugs or regimens for cardiovascular protection. Statins possess properties such as antioxidative stress, anti-inflammatory effects, antifibrotic activity, endothelial protection, and immune modulation. These pathological processes are central to the cardiotoxicity associated with anticancer treatment. There is prospective clinical evidence confirming the protective role of statins in chemotherapy-induced cardiotoxicity. Numerous preclinical studies have demonstrated that statins can ameliorate heart and endothelial damage caused by radiotherapy, although clinical studies are scarce. In the animal models of trastuzumab-induced cardiomyopathy, statins provide protection through anti-inflammatory, antioxidant, and antifibrotic mechanisms. In animal and cell models, statins can mitigate inflammation, endothelial damage, and cardiac injury induced by immune checkpoint inhibitors. Chimeric antigen receptor (CAR)-T cell therapy-induced cardiotoxicity and immune effector cell-associated neurotoxicity syndrome are associated with uncontrolled inflammation and immune activation. Due to their anti-inflammatory and immunomodulatory effects, statins have been used to manage CAR-T cell therapy-induced immune effector cell-associated neurotoxicity syndrome in a clinical trial. However, direct evidence proving that statins can mitigate CAR-T cell therapy-induced cardiotoxicity is still lacking. This review summarizes the possible mechanisms of anticancer therapy-induced cardiotoxicity and the potential mechanisms by which statins may reduce related cardiac damage. We also discuss the current status of research on the protective effect of statins in anticancer treatment-related cardiovascular disease and provide directions for future research. Additionally, we propose further studies on using statins for the prevention of cardiovascular disease in anticancer treatment.
某些抗癌疗法不可避免地会增加心血管事件的风险,而心血管疾病现在是癌症患者的第二大死亡原因。这凸显了开发有效药物或方案以保护心血管的迫切需求。他汀类药物具有抗氧化应激、抗炎作用、抗纤维化活性、内皮保护和免疫调节等特性。这些病理过程是与抗癌治疗相关的心脏毒性的核心。有前瞻性临床证据证实他汀类药物在化疗引起的心脏毒性中的保护作用。大量临床前研究表明,他汀类药物可以改善放疗引起的心脏和内皮损伤,尽管临床研究较少。在曲妥珠单抗诱导的心肌病的动物模型中,他汀类药物通过抗炎、抗氧化和抗纤维化机制提供保护。在动物和细胞模型中,他汀类药物可以减轻免疫检查点抑制剂引起的炎症、内皮损伤和心脏损伤。嵌合抗原受体 (CAR)-T 细胞治疗诱导的心肌病和免疫效应细胞相关神经毒性综合征与不受控制的炎症和免疫激活有关。由于他汀类药物具有抗炎和免疫调节作用,因此已在临床试验中用于治疗 CAR-T 细胞治疗诱导的免疫效应细胞相关神经毒性综合征。然而,直接证明他汀类药物可以减轻 CAR-T 细胞治疗诱导的心脏毒性的证据仍然缺乏。本综述总结了抗癌治疗引起的心脏毒性的可能机制以及他汀类药物可能减轻相关心脏损伤的潜在机制。我们还讨论了他汀类药物在抗癌治疗相关心血管疾病中的保护作用的研究现状,并为未来的研究提供了方向。此外,我们提出了在抗癌治疗中使用他汀类药物预防心血管疾病的进一步研究。