Todorova Valentina K, Makhoul Issam, Wei Jeanne, Klimberg V S
Department of Surgery/Breast Surgical Oncology, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Department of Hematology/Oncology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Ann Clin Lab Sci. 2017 Mar;47(2):115-119.
Doxorubicin (DOX) cardiotoxicity is unpredictable and begins with the first dose of chemotherapy. This study aimed to obtain information about circulating microRNA of cancer patients in the early dose of DOX chemotherapy, who either did or did not develop cardiac abnormality after the completion of chemotherapy. Plasma of 20 patients treated for breast cancer with DOX-chemotherapy was analyzed using quantitative RT-PCR. Circulating microRNA profiles of patients with DOX cardiotoxicity were compared to microRNA profiles of patients without DOX cardiotoxicity by quantitative real-time PCR. Thirty-two microRNAs were significantly dysregulated in the patients with abnormal cardiac function. Functional analysis of the 32 miRNAs suggested association with cell death, cell cycle, and inflammation. We have identified a miRNA signature associated with early doses of DOX-based chemotherapy that may potentially predict later impairment of cardiac function in breast cancer patients. Our data lay a foundation for future studies to identify biomarkers for presymptomatic DOX-induced cardiotoxicity.
阿霉素(DOX)的心脏毒性不可预测,且从化疗的第一剂就开始出现。本研究旨在获取有关接受DOX化疗早期阶段癌症患者循环微RNA的信息,这些患者在化疗结束后出现或未出现心脏异常。使用定量逆转录聚合酶链反应(RT-PCR)分析了20例接受DOX化疗的乳腺癌患者的血浆。通过定量实时PCR将DOX心脏毒性患者的循环微RNA谱与无DOX心脏毒性患者的微RNA谱进行比较。32种微RNA在心脏功能异常的患者中显著失调。对这32种微RNA的功能分析表明它们与细胞死亡、细胞周期和炎症相关。我们已经确定了一种与基于DOX的早期化疗相关的微RNA特征,它可能潜在地预测乳腺癌患者后期的心脏功能损害。我们的数据为未来研究确定症状前DOX诱导心脏毒性的生物标志物奠定了基础。