Early detection of anthracycline-induced cardiotoxicity

被引:0
|
作者
Feng, Weimin
Wang, Qingchen
Tan, Yuan
Qiao, Jiao
Liu, Qi
Yang, Boxin
Yang, Shuo
Cui, Liyan [1 ]
机构
[1] Peking Univ Third Hosp, Dept Lab Med, 49 Huayuan North Rd, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
Anthracyclines; Cardiotoxicity; Mechanism; Biomarkers; Prevention; DOXORUBICIN-INDUCED CARDIOTOXICITY; DNA TOPOISOMERASE-II; BREAST-CANCER; INDUCED CARDIOMYOPATHY; MYOCARDIAL-INFARCTION; MOLECULAR-MECHANISMS; ELECTRON-TRANSPORT; TETRANECTIN LEVELS; PROMOTES SURVIVAL; OXIDATIVE STRESS;
D O I
10.1016/j.cca.2024.120000
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Although anthracyclines are important anticancer agents, their use is limited due to various adverse effects, particularly cardiac toxicity. Mechanisms underlying anthracycline-induced cardiotoxicity (AIC) are complex. Given the irreplaceable role of anthracyclines in treatment of malignancies and other serious diseases, early monitoring of AIC is paramount. In recent years, multiple studies have investigated various biomarkers for early detection of AIC. Currently, the two most common are cardiac troponin and B-type natriuretic peptide. In addition, a range of other molecules, including RNAs, myeloperoxidase (MPO), C-reactive protein (CRP), various genes, and others, also play roles in AIC prediction. Unfortunately, current research indicates a need to validate their sensitivity and specificity of these biomarkers especially in large study populations. In this review, we summarize the mechanisms and potential biomarkers of AIC, although some remain preliminary.
引用
收藏
页数:13
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