Qiu Cuipeng, Wang Peng, Wang Bofei, Shi Jianxiang, Wang Xiao, Li Tiandong, Qin Jiejie, Dai Liping, Ye Hua, Zhang Jianying
Department of Epidemiology and Health Statistics, College of Public Health, Zhengzhou University, Zhengzhou, Henan, China.
College of Public Health, Henan Key Laboratory of Tumor Epidemiology, Zhengzhou University, Zhengzhou, Henan, China.
Oncoimmunology. 2019 Oct 28;9(1):1682382. doi: 10.1080/2162402X.2019.1682382. eCollection 2020.
Serum autoantibodies that react with tumor-associated antigens (TAAs) can be used as potential biomarkers for diagnosis of cancer. This study aims to evaluate the immunodiagnostic value of 11 anti-TAAs autoantibodies for detection of breast cancer (BC) and establish a diagnostic model for distinguishing BC from normal human controls (NHC) and benign breast diseases (BBD). Sera from 10 BC patients and 10 NHC were used to detect 11 anti-TAAs autoantibodies by western blotting. The 11 anti-TAAs autoantibodies were further assessed in 983 sera by relative quantitative enzyme-linked immunosorbent assay (ELISA). Binary logistic regression and Fisher linear discriminant analysis were conducted to establish a prediction model by using 184 BC and 184 NHC (training cohort, n = 568) and validated by leave-one-out cross-validation. Logistic regression model was selected to establish the prediction model. Results were validated using an independent validation cohort (n = 415). The five anti-TAAs (p53, cyclinB1, p16, p62, 14-3-3ξ) autoantibodies were selected to construct the model with the area under the curve (AUC) of 0.943 (95% CI, 0.919-0.967) in training cohort and 0.916 (95% CI, 0.886-0.947) in the validation cohort. In the identification of BC and BBD, AUCs were 0.881 (95% CI, 0.848-0.914) and 0.849 (95% CI, 0.803-0.894) in training and validation cohort, respectively. In summary, our study indicates that the immunodiagnostic model can distinguish BC from NHC and BC from BBD and this model may have a potential application in immunodiagnosis of breast cancer.
与肿瘤相关抗原(TAA)发生反应的血清自身抗体可作为癌症诊断的潜在生物标志物。本研究旨在评估11种抗TAA自身抗体对乳腺癌(BC)检测的免疫诊断价值,并建立一种用于区分BC与正常对照人群(NHC)以及良性乳腺疾病(BBD)的诊断模型。采用蛋白质印迹法检测10例BC患者和10例NHC血清中的11种抗TAA自身抗体。通过相对定量酶联免疫吸附测定(ELISA)对983份血清中的11种抗TAA自身抗体进行进一步评估。利用184例BC患者和184例NHC(训练队列,n = 568)进行二元逻辑回归和Fisher线性判别分析以建立预测模型,并通过留一法交叉验证进行验证。选择逻辑回归模型建立预测模型。使用独立验证队列(n = 415)对结果进行验证。选择5种抗TAA(p53、细胞周期蛋白B1、p16、p62、14-3-3ξ)自身抗体构建模型,训练队列中的曲线下面积(AUC)为0.943(95%CI,0.919 - 0.967),验证队列中的AUC为0.916(95%CI,0.886 - 0.947)。在区分BC与BBD时,训练队列和验证队列中的AUC分别为0.881(95%CI,0.848 - 0.914)和0.849(95%CI,0.803 - 0.894)。总之,我们的研究表明该免疫诊断模型能够区分BC与NHC以及BC与BBD,且该模型可能在乳腺癌的免疫诊断中具有潜在应用价值。