中药治疗抗癌药物引发心脏毒性的研究进展

苏琳玲 ,  袁仙霞 ,  江文瑜 ,  莫岭 ,  吴佳雪 ,  王敏 ,  刘东玲 ,  海洋

中国药科大学学报 ›› 2026, Vol. 57 ›› Issue (3) : 393 -400.

PDF (576KB)
中国药科大学学报 ›› 2026, Vol. 57 ›› Issue (3) : 393 -400. DOI: 10.11665/j.issn.1000−5048.2025112103
综述

中药治疗抗癌药物引发心脏毒性的研究进展

作者信息 +

Research progress on traditional Chinese medicine in treating cardiotoxicity induced by anticancer drugs

Author information +
文章历史 +
PDF (589K)

摘要

抗癌药物所致心脏毒性是影响肿瘤患者预后的重要因素。本文系统归纳了化疗药、分子靶向治疗药和免疫治疗药引发心脏毒性的临床表征,并指出其核心毒性机制涉及心肌细胞凋亡、氧化应激失衡及线粒体功能障碍等。在中医理论中,抗癌药导致的心脏毒性属“热毒”范畴,其核心病机是气血不足、心火亢盛、心血瘀阻、痰湿阻滞。因此,本文通过梳理补虚药、清热药、活血祛瘀药、化痰止咳平喘药和温里药的防治作用及机制,发现其组方原则为“扶正解毒祛瘀”,这些中药主要通过抗氧化应激、调节自噬平衡、抑制炎症反应、改善微循环等机制发挥防治作用。上述作用机制与现代医学治疗策略(如右雷佐生抑制铁依赖性氧化应激、他汀类药物抗炎等)高度契合。本文旨在为中西医协同精准防治抗癌药物心脏毒性提供理论支撑与实践参考。

Abstract

Cardiotoxicity induced by antineoplastic agents is an important factor affecting the prognosis of cancer patients. This article systematically summarizes the clinical manifestations of cardiotoxicity caused by chemotherapeutic drugs, molecular targeted cancer therapies, and immunotherapeutic drugs, and identifies the core injury mechanisms, including cardiomyocyte apoptosis, oxidative stress, and mitochondrial dysfunction. In Traditional Chinese Medicine (TCM) theory, anticancer drug-induced cardiotoxicity falls under the category of “heat toxins” characterized by dual deficiency of qi and blood, upward flaming of heart heat, stagnation of the heart vessels, and meridian obstruction induced by phlegm-dampness. Therefore, by reviewing the preventive and therapeutic effects and the underlying mechanisms of tonic medicines, interior heat-clearing medicines, blood-circulating and stasis-resolving medicines, phlegm-transforming, cough-suppressing and panting-relieving medicines, and interior-warming medicines, this paper concludes that TCM prevention and treatment of this condition adheres to the formulation principle of “reinforcing healthy qi, removing toxins, and resolving blood stasis”. Its mechanisms of action—including antioxidation effects, regulation of autophagic balance, antagonism of inflammatory responses, and improvement of microcirculation—are highly consistent with modern medical treatment strategies (e.g., dexrazoxane for inhibiting iron-dependent oxidative stress, statins for anti-inflammatory effects). This study provides theoretical support and practical guidance for the collaborative and precise prevention and treatment of anticancer drug-induced cardiotoxicity through the integration of traditional Chinese and Western medicine.

关键词

癌症 / 肿瘤心脏病 / 心脏毒性 / 中药 / 抗癌药

Key words

cancer / cardio-oncology disease / cardiotoxicity / traditional Chinese medicine / anticancer drugs

引用本文

引用格式 ▾
苏琳玲,袁仙霞,江文瑜,莫岭,吴佳雪,王敏,刘东玲,海洋. 中药治疗抗癌药物引发心脏毒性的研究进展[J]. 中国药科大学学报, 2026, 57(3): 393-400 DOI:10.11665/j.issn.1000−5048.2025112103

登录浏览全文

4963

注册一个新账户 忘记密码

参考文献

[1]

Qi HT, Zhang XT. Research advances in the mechanism, prevention, and treatment of cardiotoxicity induced by antineoplastic agents[J]. J Qingdao Univ Med Sci(青岛大学学报), 2021, 57(2): 309—313.

[2]

O'Connell TX, Berenbaum MC. Cardiac and pulmonary effects of high doses of cyclophosphamide and isophosphamide[J]. Cancer Res. 1974, 34(7): 1586-91.

[3]

Lefrak EA, Piťha J, Rosenheim S, et al. A clinicopathologic analysis of adriamycin cardiotoxicity[J]. Cancer, 1973, 32(2): 302-314.

[4]

Ghione M. Cardiotoxic effects of antitumor agents[J]. Cancer Chemother Pharmacol, 1978, 1(1): 25-34.

[5]

Tocchetti CG, Farmakis D, Koop Y, et al. Cardiovascular toxicities of immune therapies for cancer—a scientific statement of the Heart Failure Association (HFA) of the ESC and the ESC Council of Cardio—Oncology[J]. Eur J Heart Fail, 2024, 26(10): 2055-2076.

[6]

Becker RC. Immune checkpoint inhibitors and cardiovascular toxicity: immunology, pathophysiology, diagnosis, and management[J]. J Thromb Thrombolysis, 2025, 58(8): 1021-1044.

[7]

Ito—Hagiwara K, Hagiwara J, Endo Y, et al. Cardioprotective strategies against doxorubicin—induced cardiotoxicity: a review from standard therapies to emerging mitochondrial transplantation[J]. Biomed Pharmacother, 2025, 189: 118315.

[8]

Hara A. Anthracycline—induced cardiotoxicity and exploration of cardioprotective drugs[J]. Yakugaku Zasshi, 2025, 145(2): 121-132.

[9]

Migliari M, Fazzini L, Campana N, et al. Current strategies for prevention of cancer therapy—related cardiotoxicity: pharmacological, non—pharmacological and emerging approaches[J]. Front Cardiovasc Med, 2025, 12: 1668308.

[10]

Yu MJ, Yang RH. Clinical trial of dexrazoxane injection in preventing anthracycline induced cardiotoxicity in breast cancer patients[J]. Chin J Clin Pharmacol (中国临床药理学杂志), 2022, 38(7): 627—630.

[11]

Zhi T, Zhang WL, Zhang Y, et al. Protective effect of amifostine in the chemotherapy of malignant solid tumor in children[J]. Cancer Res Clin(肿瘤研究与临床), 2021, 33(1): 53—56.

[12]

Wang XP, Li C, Wang QY, et al. Tanshinone IIA restores dynamic balance of autophagosome/autolysosome in doxorubicin—induced cardiotoxicityvia targeting Beclin1/LAMP1[J]. Cancers, 2019, 11(7): 910.

[13]

Zhang JY, Wang M, Wang RY, et al. Salvianolic acid a ameliorates arsenic trioxide—induced cardiotoxicity through decreasing cardiac mitochondrial injury and promotes its anticancer activity[J]. Front Pharmacol, 2018, 9: 487.

[14]

Alizadehasl A, Shahrami B, Rahbarghazi R, et al. Post—transplant cyclophosphamide—induced cardiotoxicity: a comprehensive review[J]. J Cardiovasc Thorac Res, 2024, 16(4): 211-221.

[15]

Fabiani I, Chianca M, Cipolla CM, et al. Anthracycline—induced cardiomyopathy: risk prediction, prevention and treatment[J]. Nat Rev Cardiol, 2025, 22(8): 551-563.

[16]

Moghadamnia A, Karim B, Ebrahimi P, et al. 5—Fluorouracil (5—FU)—induced organ toxicities: mechanisms, management, and prevention strategies[J]. Toxicol Mech Meth, 2026, 36(1): 1-28.

[17]

Joshi AM, Prousi GS, Bianco C, et al. Microtubule inhibitors and cardiotoxicity[J]. Curr Oncol Rep, 2021, 23(3): 30.

[18]

Jiang YN, Shen XY, Zhi FN, et al. An overview of arsenic trioxide—involved combined treatment algorithms for leukemia: basic concepts and clinical implications[J]. Cell Death Discov, 2023, 9: 266.

[19]

Zhang Y, Deng JG, Wang JZ. Cardiovascular toxicities associated with vascular endothelial growth factor receptor tyrosine kinase inhibitors: a pharmacovigilance study based on FDA adverse event reporting system[J]. Int J Clin Pharm, 2025, 47(5): 1467-1474.

[20]

Mihalcea D, Memis H, Mihaila S, et al. Cardiovascular toxicity induced by vascular endothelial growth factor inhibitors[J]. Life, 2023, 13(2): 366.

[21]

Xiao LF, Lin XL, Yang ZN, et al. Heart failure induced by cancer therapies: focus on targeted agents, mechanisms, risk prediction, and clinical management[J]. Front Pharmacol, 2026, 17: 1766603.

[22]

Quartermaine C, Ghazi SM, Yasin A, et al. Cardiovascular toxicities of BTK inhibitors in chronic lymphocytic leukemia JACC: CardioOncology state—of—the—art review[J]. JACC CardioOncology, 2023, 5(5): 570-590.

[23]

Gao Y, Zhou D, Bai X, et al. Carfilzomib in multiple myeloma: unraveling cardiac toxicities—from mechanisms to diagnosis and management[J]. Front Pharmacol, 2025, 16: 1570017.

[24]

Duane C, Glavey S, Quinn J, et al. Significant risk of venous thromboembolism associated with targeted anti—myeloma immunomodulatory drugs. Comment on: Targeted anti—cancer agents and risk of venous thromboembolism[J]. Haematologica, 2025, 110(10): 2552-2553.

[25]

Miao L. Study on the regulatory effect of Shenqi buqi granules in improving energy metabolism of chronic heart failure based on omics technology(基于组学技术探究参芪补气颗粒改善慢性心衰能量代谢的调控作用)[D]. Beijing: China Academy of Chinese Medical Sciences, 2023.

[26]

Zhu KX, Wu M, Bian ZL, et al. Exploring the theoretical innovation and clinical practice of balancing Yin and Yang in the treatment of chronic kidney disease based on autophagy regulation[J]. Glob Tradit Chin Med (环球中医药), 2024, 17(8): 1573—1579.

[27]

Han JY, Pan DY, Xiao JX, et al. Mechanism of ferroptosis in cerebral ischemia—reperfusion and interventional mechanism of Huoxue Huayu Jiedu prescription based on “blood stasis and toxin” pathogenesis[J]. Chin J Exp Tradit Med Formulae (中国实验方剂学杂志), 2025, 31(8): 51—60.

[28]

Lin JM, Fang LJ, Li H, et al. Astragaloside IV alleviates doxorubicin induced cardiomyopathy by inhibiting NADPH oxidase derived oxidative stress[J]. Eur J Pharmacol, 2019, 859: 172490.

[29]

Li YY, Zhou XZ, Lei XH, et al. The experimental study on astragaloside IV regulating mitochondrial autophagy to reduce myocardial toxicity induced by 5—Fu in aging rats[J]. Tianjin Med J (天津医药), 2021, 49(4): 378—384.

[30]

Hou JG, Yun Y, Cui CH, et al. Ginsenoside Rh2 mitigates doxorubicin—induced cardiotoxicity by inhibiting apoptotic and inflammatory damage and weakening pathological remodelling in breast cancer—bearing mice[J]. Cell Prolif, 2022, 55(6): e13246.

[31]

Xu ZB, Hu ZD, Xu HC, et al. Liquiritigenin alleviates doxorubicin—induced chronic heart failure via promoting ARHGAP18 and suppressing RhoA/ROCK1 pathway[J]. Exp Cell Res, 2022, 411(2): 113008.

[32]

Cheng YF, Wu XP, Nie X, et al. Natural compound glycyrrhetinic acid protects against doxorubicin—induced cardiotoxicity by activating the Nrf2/HO—1 signaling pathway[J]. Phytomedicine, 2022, 106: 154407.

[33]

Liu M, Liquiritin regulates the SLC7A11/GPX4 pathway inhibition of cardiotoxicity of doxorubicin—induced ferroptosis in cardiomyocytes (甘草苷调控SLC7A11/GPX4信号通路预防阿霉素心脏毒性的机制研究)[D]. Hengyang: University of South China, 2022.

[34]

Zhang XX, Zhang Q, Yu MH, et al. Integrating serum pharmacochemistry and network pharmacology to explore the molecular mechanisms of Acanthopanax senticosus (Rupr. & Maxim.) Harms on attenuating doxorubicin—induced myocardial injury[J]. J Ethnopharmacol, 2024, 319: 117349.

[35]

Chen H, Zhu J, Le YF, et al. Salidroside inhibits doxorubicin—induced cardiomyopathy by modulating a ferroptosis—dependent pathway[J]. Phytomedicine, 2022, 99: 153964.

[36]

Zhang SJ, Tian RQ, Ding YC, et al. Effects of paeoniflorin on cardiac dysfunction and myocardial cell injury induced by cisplatin in rats based on ERK/p38 MAPK signaling pathway[J]. Chin J Mod Appl Pharm (中国现代应用药学), 2024, 41(11): 1476—1483.

[37]

Wu R, Yao PA, Wang HL, et al. Effect of fermented Cordyceps sinensis on doxorubicin—induced cardiotoxicity in rats[J]. Mol Med Report, 2018, 18(3): 3229-3241.

[38]

Zhuang JL, Zhu J, Dou Y, et al. Shenqi Lixin Decoction improves cardiac function in rats with adriamycin—induced heart failure through modulation of PGC—1α and mitochondrial apoptosis pathway[J]. Ann Transl Med, 2021, 9(20): 1592.

[39]

Wang LJ, Wang LY, Zhou XX, et al. Qishen Yiqi dropping pills ameliorates doxorubicin—induced cardiotoxicity in mice via enhancement of cardiac angiogenesis[J]. Med Sci Monit, 2019, 25: 2435-2444.

[40]

Ren DZ, Li F, Cao QW, et al. Yangxin granules alleviate doxorubicin—induced cardiotoxicity by suppressing oxidative stress and apoptosis mediated by AKT/GSK3β/β—catenin signaling[J]. J Int Med Res, 2020, 48(8): 0300060520945161.

[41]

Chen T, Shen HM, Deng ZY, et al. A herbal formula, SYKT, reverses doxorubicin—induced myelosuppression and cardiotoxicity by inhibiting ROS—mediated apoptosis[J]. Mol Med Rep, 2017, 15(4): 2057-2066.

[42]

Huang CY, Qiu S, Fan XC, et al. Evaluation of the effect of Shengxian Decoction on doxorubicin—induced chronic heart failure model rats and a multicomponent comparative pharmacokinetic study after oral administration in normal and model rats[J]. Biomed Pharmacother, 2021, 144: 112354.

[43]

Liu K, Ren XM, You QS, et al. Ameliorative effect of dangguibuxue decoction against cyclophosphamide—induced heart injury in mice[J]. BioMed Res Int, 2018, 2018(1): 8503109.

[44]

Gao L, Yang T, Zhu J, et al. Effect of Qiangxin Huoli decoction on rats with adriamycin—induced chronic heart failure[J]. J Tradit Chin Med, 2019, 39(1): 81-88.

[45]

Yuan CY, Wu Z, Jin CL, et al. Qiangxin recipe improves doxorubicin—induced chronic heart failure by enhancing KLF5—mediated glucose metabolism[J]. Phytomedicine, 2023, 112: 154697.

[46]

You JS, Huang HF, Chang YL, et al. Sheng—Mai—San reduces adriamycin—induced cardiomyopathy in rats[J]. Am J Chin Med, 2006, 34(2): 295-305.

[47]

Zhang S, You ZQ, Yang L, et al. Protective effect of Shenmai injection on doxorubicin—induced cardiotoxicity via regulation of inflammatory mediators[J]. BMC Complement Altern Med, 2019, 19(1): 317.

[48]

Cui YM, Li CH, Zeng C, et al. Tongmai Yangxin pills anti—oxidative stress alleviates cisplatin—induced cardiotoxicity: network pharmacology analysis and experimental evidence[J]. Biomed Pharmacother, 2018, 108: 1081-1089.

[49]

Zhang JM, Li WL, Xue SM, et al. Qishen granule attenuates doxorubicin—induced cardiotoxicity by protecting mitochondrial function and reducing oxidative stress through regulation of Sirtuin3[J]. J Ethnopharmacol, 2024, 319: 117134.

[50]

Wang F, Wang LX, Jiao Y, et al. Qishen Huanwu capsule reduces pirarubicin—induced cardiotoxicity in rats by activating the PI3K/Akt/mTOR pathway[J]. Ann Palliat Med, 2020, 9(5): 3453-3461.

[51]

Hu YX, Cao BN, Wang L, et al. Exploring the pathogenesis of “internal heat leading to Zheng” in diabetic kidney disease from the perspective of “glucose toxicity” and its differential diagnosis and treatment[J]. J Beijing Univ Tradit Chin Med (北京中医药大学学报), 2025, 48(3): 386—391.

[52]

Wang XY, Liu LT, Wu M. Treatment of cardio—oncologic diseases from the perspective of “deficiency, blood stasis, and toxicity”[J]. J Hunan Univ Chin Med (湖南中医药大学学报), 2024, 44(12): 2309—2314.

[53]

Cui H, Xu WQ, Liu L, et al. Diosgenin alleviates arsenic trioxide induced cardiac fibrosis by inhibiting endothelial mesenchymal transition[J]. Phytomedicine, 2024, 132: 155891.

[54]

Qu JM, Ke F, Yang X, et al. Induction of P—glycoprotein expression by dandelion in tumor and heart tissues: impact on the anti—tumor activity and cardiotoxicity of doxorubicin[J]. Phytomedicine, 2022, 104: 154275.

[55]

Li MJ, Sun WS, Yuan Y, et al. Breviscapine remodels myocardial glucose and lipid metabolism by regulating serotonin to alleviate doxorubicin—induced cardiotoxicity[J]. Front Pharmacol, 2022, 13: 930835.

[56]

Zhang HJ, Chen RC, Sun GB, et al. Protective effects of total flavonoids fromClinopodium chinense (Benth.) O. Ktze on myocardial injury in vivo and in vitro via regulation of Akt/Nrf2/HO—1 pathway[J]. Phytomedicine, 2018, 40: 88-97.

[57]

Feng PP, Yang Y, Liu N, et al. Baicalin regulates TLR4/IκBα/NFκB signaling pathway to alleviate inflammation in Doxorubicin related cardiotoxicity[J]. Biochem Biophys Res Commun, 2022, 637: 1-8.

[58]

Cheng S, Chen XY, Pan LL, et al. Effect of total alkaloids from Nandina domfestica in attenuating arsenic trioxide and its LC—MS[J]. Chin J Exp Tradit Med Formulae (中国实验方剂学杂志), 2020, 26(9): 129—135.

[59]

Lu Y, Liu W, Lv T, et al. Aidi injection reduces doxorubicin—induced cardiotoxicity by inhibiting carbonyl reductase 1 expression[J]. Pharm Biol, 2022, 60(1): 1616-1624.

[60]

Hao W, Liu S. Research progress on prevention of anthracycline—induced cardiotoxicity by Chinese medicine[J]. Shanghai J Tradit Chin Med (上海中医药杂志), 2016, 50(6): 99—102.

[61]

Yang XH, Zhi H, Ai D, et al. Effect of total flavonoids of fructus choerospondiatis on arsenic trioxide—induced cardiomyocyte injury[J]. China Med Her (中国医药导报), 2021, 18(20): 25—29.

[62]

Shi YY, Wu YY, Shen M, et al. Extract of Platycodon grandiflorum prevents doxorubicin—induced cardiotoxicity in breast cancer[J]. Integr Cancer Ther, 2023, 22: 15347354231164621.

[63]

Gao JQ, Chen T, Zhao DQ, et al. Ginkgolide B exerts cardioprotective properties against doxorubicin—induced cardiotoxicity by regulating reactive oxygen species, Akt and calcium signaling pathways in vitro and in vivo[J]. PLoS One, 2016, 11(12): e0168219.

[64]

Sun XT, Song YJ, Xie Y, et al. Shenlijia attenuates doxorubicin—induced chronic heart failure by inhibiting cardiac fibrosis[J]. Evid Based Complementary Altern Med, 2021, 2021(1): 6659676.

[65]

Mao MJ, Zheng W, Deng B, et al. Cinnamaldehyde alleviates doxorubicin—induced cardiotoxicity by decreasing oxidative stress and ferroptosis in cardiomyocytes[J]. PLoS One, 2023, 18(10): e0292124.

[66]

Tai PP, Chen XY, Jia GH, et al. WGX50 mitigates doxorubicin—induced cardiotoxicity through inhibition of mitochondrial ROS and ferroptosis[J]. J Transl Med, 2023, 21(1): 823.

[67]

Ding X, Zhang Y, Pan PC, et al. Multiple mitochondria—targeted components screened from Sini decoction improved cardiac energetics and mitochondrial dysfunction to attenuate doxorubicin—induced cardiomyopathy[J]. Theranostics, 2023, 13(2): 510-530.

[68]

Feng K, Liu YX, Sun J, et al. Compound Danshen Dripping Pill inhibits doxorubicin or isoproterenol—induced cardiotoxicity[J]. Biomed Pharmacother, 2021, 138: 111531.

[69]

Xu L, Hai Y, Ren K, et al. Study on the mechanism of Astragalus glycyrrhiza decoction regulating SIRT1/FOXO1 pathway to prevent QT interval prolongation induced by arsenic trioxide based on metabolomics[J]. Chin J Clin Pharmacol Ther (中国临床药理学与治疗学), 2024, 29(2): 130—138.

[70]

Center for Drug Evaluation. Guideline for Drug Interaction Studies (Trial)[药物相互作用研究技术指导原则(试行)][S]. Beijing: National Medical Products Administration, 2021: 8—9.

基金资助

国家自然科学基金项目(82260792)

甘肃省青年人才项目(2025QNGR2)

甘肃中医药大学研究生“创新创业基金”项目(2025CXCY-037)

AI Summary AI Mindmap
PDF (576KB)

0

访问

0

被引

详细

导航
相关文章

AI思维导图

/