Department of Gynecology and Obstetrics, Medical Faculty and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
National Center for Tumor Diseases (NCT), Dresden, Germany: German Cancer Research Center (DKFZ), Heidelberg, Germany; Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany, Helmholtz-Zentrum Dresden-Rossendorf (HZDR), Dresden, Germany.
Int J Cancer. 2020 May 1;146(9):2608-2618. doi: 10.1002/ijc.32676. Epub 2019 Nov 6.
Calretinin (CRT) is a calcium-binding protein that controls intracellular calcium signaling. Besides its prominent expression in neurons, serum CRT (sCRT) has recently been suggested as blood-based biomarker for prediagnostic mesothelioma detection. CRT is expressed in ovarian cancer tissues in up to 40% of cases; however, its clinical relevance as blood-based biomarker for ovarian cancer is unknown. sCRT was determined by calretinin enzyme-linked immunoabsorbent assay (Calretinin-ELISA, DLD Diagnostika GmbH, Hamburg, Germany) in a total of 515 serum samples from 116 healthy controls and 134 ovarian cancer patients (thereof 86% with Fédération Internationale de Gynécologie et d'Obstétrique [FIGO] III/IV), including samples at primary diagnosis and at four longitudinal follow-up time points in the course of treatment and at recurrence. sCRT level was significantly increased in ovarian cancer patients compared to healthy controls (estimated difference = 0.3 ng/ml, p < 0.001), was mostly independent from CA125 (r ≤ 0.388) and enabled accurate discrimination between cases and controls (area under the curve = 0.85). Higher sCRT level at primary diagnosis predicted suboptimal debulking (p < 0.001) and was associated with advanced FIGO-stage (p < 0.001) and increased amount of ascites (p < 0.001). sCRT levels at primary diagnosis and its dynamics in the course of chemotherapy were independent predictors for poor progression-free survival (hazard ratio [HR] = 1.99, confidence interval [CI] = [1.13-3.52], p = 0.0181) and overall survival (HR = 15.4, CI = [1.92-124], p = 0.0099). Furthermore, sCRT at primary diagnosis or a relative sCRT increase in the time interval between surgery and the onset of chemotherapy were both independent predictors of platinum resistance (OR = 4.99, CI = [3.50-16,001], p = 0.0016; OR = 2.41, CI = [1.37-6,026], p = 0.0271, respectively). This is the first study that suggests sCRT as liquid biopsy marker for independent prediction of platinum resistance and prognosis.
钙结合蛋白 CRT 可控制细胞内钙信号转导。除了在神经元中有明显表达外,血清 CRT(sCRT)最近也被提出作为间皮瘤早期诊断的血液生物标志物。在高达 40%的卵巢癌组织中表达 CRT;然而,其作为卵巢癌血液生物标志物的临床相关性尚不清楚。在总共 515 份血清样本中,通过 calretinin 酶联免疫吸附测定(Calretinin-ELISA,DLD Diagnostika GmbH,汉堡,德国)检测了 116 名健康对照者和 134 名卵巢癌患者(其中 86%为国际妇产科联合会[FIGO] III/IV)的 sCRT,包括初诊时和治疗过程中四个纵向随访时间点以及复发时的样本。与健康对照组相比,卵巢癌患者的 sCRT 水平显著升高(估计差值=0.3ng/ml,p<0.001),与 CA125 大多独立(r≤0.388),能够准确区分病例和对照组(曲线下面积=0.85)。初诊时 sCRT 水平较高预示着减瘤效果不佳(p<0.001),与 FIGO 晚期(p<0.001)和腹水增多(p<0.001)有关。初诊时 sCRT 水平及其在化疗过程中的动态变化是无进展生存期(风险比[HR]=1.99,置信区间[CI] = [1.13-3.52],p=0.0181)和总生存期(HR=15.4,CI=[1.92-124],p=0.0099)不良的独立预测因子。此外,初诊时 sCRT 或手术与化疗开始之间时间间隔内 sCRT 的相对增加均是铂类耐药的独立预测因子(OR=4.99,CI=[3.50-16001],p=0.0016;OR=2.41,CI=[1.37-6026],p=0.0271)。这是第一项表明 sCRT 可作为独立预测铂类耐药和预后的液体活检标志物的研究。