Division of Hematology/Oncology, Department of Internal Medicine, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Department of Geriatrics, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Int J Mol Sci. 2024 Sep 9;25(17):9735. doi: 10.3390/ijms25179735.
Doxorubicin (DOX), a commonly used anticancer agent, causes cardiotoxicity that begins with the first dose and may progress to heart failure years after treatment. An inflammatory response associated with neutrophil recruitment has been recognized as a mechanism of DOX-induced cardiotoxicity. This study aimed to validate mRNA expression of the previously identified biomarkers of DOX-induced cardiotoxicity, PGLYRP1, CAMP, MMP9, and CEACAM8, and to assay their protein expression in the peripheral blood of breast cancer patients. Blood samples from 40 breast cancer patients treated with DOX-based chemotherapy were collected before and after the first chemotherapy cycle and > 2 years after treatment. The protein and gene expression of PGLYRP1/Tag7, CAMP/LL37, MMP9/gelatinase B, and CEACAM8/CD66b were determined using ELISA and reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Receiver operating characteristic (ROC) curve analysis was used to determine the diagnostic value of each candidate biomarker. Patients with cardiotoxicity (n = 20) had significantly elevated levels of PGLYRP1, CAMP, MMP9, and CEACAM8 at baseline, after the first dose of DOX-based chemotherapy, and at > 2 years after treatment relative to patients without cardiotoxicity (n = 20). The first dose of DOX induced significantly higher levels of all examined biomarkers in both groups of patients. At > 2 years post treatment, the levels of all but MMP9 dropped below the baseline. There was a good correlation between the expression of mRNA and the target proteins. We demonstrate that circulating levels of PGLYRP1, CAMP, MMP9, and CEACAM8 can predict the cardiotoxicity of DOX. This novel finding may be of value in the early identification of patients at risk for cardiotoxicity.
多柔比星(DOX)是一种常用的抗癌药物,会导致心脏毒性,这种毒性从第一次用药就开始出现,并可能在治疗后多年发展为心力衰竭。与中性粒细胞募集相关的炎症反应已被认为是 DOX 诱导心脏毒性的一种机制。本研究旨在验证先前确定的 DOX 诱导心脏毒性的生物标志物 PGLYRP1、CAMP、MMP9 和 CEACAM8 的 mRNA 表达,并检测其在乳腺癌患者外周血中的蛋白表达。采集 40 例接受 DOX 为基础的化疗的乳腺癌患者在第一次化疗周期前后和治疗 2 年以上的血液样本。使用 ELISA 和逆转录定量聚合酶链反应(RT-qPCR)检测 PGLYRP1/Tag7、CAMP/LL37、MMP9/明胶酶 B 和 CEACAM8/CD66b 的蛋白和基因表达。采用受试者工作特征(ROC)曲线分析确定每个候选生物标志物的诊断价值。有心脏毒性的患者(n = 20)在基线时、接受 DOX 为基础的化疗第一剂后和治疗 2 年以上时,PGLYRP1、CAMP、MMP9 和 CEACAM8 的水平明显升高,而无心脏毒性的患者(n = 20)则没有。两组患者在接受 DOX 第一剂后,所有检测到的生物标志物水平均显著升高。在治疗 2 年以上时,除 MMP9 外,所有标志物的水平均降至基线以下。mRNA 表达与靶蛋白之间存在良好的相关性。我们证明,循环中 PGLYRP1、CAMP、MMP9 和 CEACAM8 的水平可以预测 DOX 的心脏毒性。这一新发现可能有助于早期识别有心脏毒性风险的患者。