Department of Medical Oncology, University Hospital (CHU) and University of Liège, Liège, Belgium.
Laboratory of Human Genetics, GIGA Research, University Hospital (CHU) and University of Liège, Liège, Belgium.
BMC Cancer. 2018 Jan 29;18(1):102. doi: 10.1186/s12885-018-4015-4.
Over time, the chance of cure after the diagnosis of breast cancer has been increasing, as a consequence of earlier diagnosis, improved diagnostic procedures and more effective treatment options. However, oncologists are concerned by the risk of long term treatment side effects, including congestive heart failure (CHF).
In this study, we evaluated innovative circulating cardiac biomarkers during and after anthracycline-based neoadjuvant chemotherapy (NAC) in breast cancer patients. Levels of cardiac-specific troponins T (cTnT), N-terminal natriuretic peptides (NT-proBNP), soluble ST2 (sST2) and 10 circulating microRNAs (miRNAs) were measured.
Under chemotherapy, we observed an elevation of cTnT and NT-proBNP levels, but also the upregulation of sST2 and of 4 CHF-related miRNAs (miR-126-3p, miR-199a-3p, miR-423-5p, miR-34a-5p). The elevations of cTnT, NT-proBNP, sST2 and CHF-related miRNAs were poorly correlated, suggesting that these molecules could provide different information.
Circulating miRNA and sST2 are potential biomarkers of the chemotherapy-related cardiac dysfunction (CRCD). Nevertheless, further studies and long-term follow-up are needed in order to evaluate if these new markers may help to predict CRCD and to identify the patients at risk to later develop CHF.
随着时间的推移,乳腺癌诊断后的治愈机会不断增加,这是由于早期诊断、改进的诊断程序和更有效的治疗选择。然而,肿瘤学家担心长期治疗副作用的风险,包括充血性心力衰竭(CHF)。
在这项研究中,我们评估了乳腺癌患者接受蒽环类药物新辅助化疗(NAC)期间和之后的创新循环心脏生物标志物。测量了心脏特异性肌钙蛋白 T(cTnT)、N 末端利钠肽(NT-proBNP)、可溶性 ST2(sST2)和 10 种循环 microRNAs(miRNAs)的水平。
在化疗过程中,我们观察到 cTnT 和 NT-proBNP 水平升高,但 sST2 和 4 种 CHF 相关 miRNAs(miR-126-3p、miR-199a-3p、miR-423-5p、miR-34a-5p)也上调。cTnT、NT-proBNP、sST2 和 CHF 相关 miRNAs 的升高相关性较差,表明这些分子可能提供不同的信息。
循环 miRNA 和 sST2 是化疗相关心脏功能障碍(CRCD)的潜在生物标志物。然而,需要进一步的研究和长期随访,以评估这些新标志物是否有助于预测 CRCD 并识别可能随后发展为 CHF 的风险患者。