Xu Yu, Zhang Wenjing, Xia Tingting, Liu Yuliang, Bi Zhoukui, Guo Liang, Xie Weijia, Xiang Ying, Xu Zhi, Yu Zubin, Li Yafei, Bai Li
Department of Respiratory and Critical Care Medicine, Xinqiao Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Department of Epidemiology, College of Preventive Medicine, Army Medical University (Third Military Medical University), Chongqing, China.
Front Oncol. 2023 Feb 15;13:1022331. doi: 10.3389/fonc.2023.1022331. eCollection 2023.
The diagnostic value of 7 tumor-associated autoantibodies (AABs) including p53, PGP9.5, SOX2, GAGE7, GBU4-5, MEGEA1, and CAGE for the detection of lung cancer has shown inconsistency in several studies. This study aimed to confirm the diagnostic value of 7AABs and to explore whether the diagnostic value would be improved by combining them with 7 traditional tumor-associated antigens (CEA, NSE, CA125, SCC, CA15-3, pro-GRP, and CYFRA21-1) in clinical settings.
The plasma levels of 7-AABs were detected by enzyme-linked immunosorbent assay (ELISA) in 533 lung cancer cases and 454 controls. The 7 tumor antigens (7-TAs) were measured by Electrochemiluminescence immunoassay with Cobas 6000 (Roche, Basel, Switzerland).
The positive rate of 7-AABs in the lung cancer group (64.00%) was significantly higher than that of healthy controls (47.90%). The 7-AABs panel was able to discriminate lung cancer from controls with a specificity of 51.50%. After combining the 7-AABs with 7-TAs, the sensitivity showed a significantly enhancement compared with 7AABs panel alone (92.09% vs 63.21%). In patients with resectable lung cancer, the combination of 7-AABs and 7-TAs improved the sensitivity from 63.52% to 97.42.
In conclusion, our study found that the diagnostic value of 7-AABs was enhanced when combined with 7-TAs. This combined panel could be used as promising biomarker to detect resectable lung cancer in clinical settings.
包括p53、PGP9.5、SOX2、GAGE7、GBU4-5、MEGEA1和CAGE在内的7种肿瘤相关自身抗体(AABs)对肺癌检测的诊断价值在多项研究中显示出不一致性。本研究旨在确认7种AABs的诊断价值,并探讨在临床环境中将它们与7种传统肿瘤相关抗原(癌胚抗原、神经元特异性烯醇化酶、癌抗原125、鳞状细胞癌抗原、癌抗原15-3、胃泌素释放肽前体和细胞角蛋白19片段)联合使用是否会提高诊断价值。
采用酶联免疫吸附测定(ELISA)检测533例肺癌患者和454例对照者血浆中7种AABs的水平。采用瑞士巴塞尔罗氏公司的Cobas 6000电化学发光免疫分析法检测7种肿瘤抗原(7-TAs)。
肺癌组7种AABs的阳性率(64.00%)显著高于健康对照组(47.90%)。7种AABs组合能够以51.50%的特异性区分肺癌与对照组。将7种AABs与7种TAs联合使用后,敏感性比单独使用7种AABs组合时有显著提高(92.09%对63.21%)。在可切除肺癌患者中,7种AABs与7种TAs联合使用使敏感性从63.52%提高到97.42%。
总之,我们的研究发现,7种AABs与7种TAs联合使用时诊断价值增强。这种联合检测组合可作为一种有前景的生物标志物,用于在临床环境中检测可切除肺癌。