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AGR3 in Breast Cancer: Prognostic Impact and Suitable Serum-Based Biomarker for Early Cancer Detection

机译:乳腺癌中的AGR3:对早期癌症的预后影响和基于血清的生物标志物

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摘要

Blood-based early detection of breast cancer has recently gained novel momentum, as liquid biopsy diagnostics is a fast emerging field. In this study, we aimed to identify secreted proteins which are up-regulated both in tumour tissue and serum samples of breast cancer patients compared to normal tissue and sera. Based on two independent tissue cohorts (n = 75 and n = 229) and one serum cohort (n = 80) of human breast cancer and healthy serum samples, we characterised AGR3 as a novel potential biomarker both for breast cancer prognosis and early breast cancer detection from blood. AGR3 expression in breast tumours is significantly associated with oestrogen receptor α (P<0.001) and lower tumour grade (P<0.01). Interestingly, AGR3 protein expression correlates with unfavourable outcome in low (G1) and intermediate (G2) grade breast tumours (multivariate hazard ratio: 2.186, 95% CI: 1.008-4.740, P<0.05) indicating an independent prognostic impact. In sera analysed by ELISA technique, AGR3 protein concentration was significantly (P<0.001) elevated in samples from breast cancer patients (n = 40, mainly low stage tumours) compared to healthy controls (n = 40). To develop a suitable biomarker panel for early breast cancer detection, we measured AGR2 protein in human serum samples in parallel. The combined AGR3/AGR2 biomarker panel achieved a sensitivity of 64.5% and a specificity of 89.5% as shown by receiver operating characteristic (ROC) curve statistics. Thus our data clearly show the potential usability of AGR3 and AGR2 as biomarkers for blood-based early detection of human breast cancer.
机译:由于液体活检诊断是一个快速发展的领域,基于血液的乳腺癌早期检测最近获得了新的动力。在这项研究中,我们旨在鉴定与正常组织和血清相比在乳腺癌患者的肿瘤组织和血清样品中均被上调的分泌蛋白。基于人类乳腺癌和健康血清样本的两个独立组织队列(n = 75和n = 229)和一个血清队列(n = 80),我们将AGR3表征为乳腺癌预后和早期乳腺癌的新型潜在生物标志物从血液中检测。乳腺肿瘤中的AGR3表达与雌激素受体α(P <0.001)和较低的肿瘤分级(P <0.01)显着相关。有趣的是,AGR3蛋白表达与低(G1)和中(G2)级乳腺肿瘤的不良预后相关(多元危险比:2.186,95%CI:1.008-4.740,P <0.05),表明有独立的预后影响。在通过ELISA技术分析的血清中,与健康对照组(n = 40)相比,乳腺癌患者(n = 40,主要是低期肿瘤)样品中的AGR3蛋白浓度显着升高(P <0.001)。为了开发适合早期乳腺癌检测的生物标志物,我们平行测量了人血清样品中的AGR2蛋白。如受体工作特性(ROC)曲线统计数据所示,组合的AGR3 / AGR2生物标志物面板实现了64.5%的灵敏度和89.5%的特异性。因此,我们的数据清楚地表明了AGR3和AGR2作为生物标记物在基于血液的人类乳腺癌早期检测中的潜在可用性。

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