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早期发现蒽环类药物诱导的心脏毒性。

Early detection of anthracycline-induced cardiotoxicity.

机构信息

Department of Laboratory Medicine, Peking University Third Hospital, No. 49 Huayuan North Road, 100191, China; Institute of Medical Technology, Peking University Health Science Center, No. 38 Xueyuan Road, Beijing, 100191, China.

出版信息

Clin Chim Acta. 2025 Jan 15;565:120000. doi: 10.1016/j.cca.2024.120000. Epub 2024 Oct 12.

Abstract

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.

摘要

尽管蒽环类药物是重要的抗癌药物,但由于各种不良反应,特别是心脏毒性,其应用受到限制。蒽环类药物引起的心脏毒性(AIC)的机制很复杂。鉴于蒽环类药物在治疗恶性肿瘤和其他严重疾病中的不可替代作用,早期监测 AIC 至关重要。近年来,多项研究探讨了各种生物标志物用于早期检测 AIC。目前,最常见的两种是心肌肌钙蛋白和 B 型利钠肽。此外,一系列其他分子,包括 RNA、髓过氧化物酶(MPO)、C 反应蛋白(CRP)、各种基因等,在 AIC 预测中也发挥作用。不幸的是,目前的研究表明需要验证这些生物标志物的敏感性和特异性,特别是在大型研究人群中。在这篇综述中,我们总结了 AIC 的机制和潜在生物标志物,尽管有些仍处于初步阶段。

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