Kato Tatsuya, Ujiie Hideki, Hatanaka Kanako C, Nange Ayae, Okumura Asami, Tsubame Kaho, Naruchi Kentato, Sato Masaharu, Kaga Kichizo, Matsuno Yoshihiro, Wakasa Satoru, Hatanaka Yutaka
Department of Cardiovascular and Thoracic Surgery, Hokkaido University Faculty and School of Medicine, Sapporo, Hokkaido 060-8638, Japan.
Clinical Research and Medical Innovation Center, Hokkaido University Hospital, Sapporo, Hokkaido, 060-8648, Japan.
Oncol Lett. 2021 Mar;21(3):202. doi: 10.3892/ol.2021.12463. Epub 2021 Jan 12.
Mucin 1 (MUC1) expression is upregulated in multiple types of cancer, including lung cancer. However, the conventional anti-MUC1 antibody is not useful for the differentiation of malignant lung tumors and benign lesions due to its limited specificity. Our previous study screened a novel epitope-defined antibody against cancer-associated sugar chain structures that specifically recognizes the MUC1 Tn antigen (MUC1-Tn ED Ab). In the present study, its potential utility as a diagnostic marker and therapeutic tool for lung adenocarcinoma (ADC) was examined. Immunohistochemical analysis of a lung ADC tissue microarray was performed using the MUC1-Tn ED Ab (clone SN-102), and the results were compared with those of another clone and commercially available MUC1 antibodies. The association between positive immunoreactivity of SN-102 and clinicopathologic factors was analyzed. Furthermore, the association between MUC1-Tn expression and epithelial-mesenchymal transition markers and radiological characteristics was analyzed. Moderate or high MUC1-Tn expression (MUC1-Tn-H) was observed in 138 (78.9%) of the 175 lung ADC cases. MUC1-Tn-H was associated with male sex, cigarette smoking, tumor extension, pleural invasion, and higher preoperative serum carcinoembryonic antigen and cytokeratin 19 fragment levels. Tumors with MUC1-Tn-H had higher consolidation/tumor ratios according to computed tomography and greater uptakes of F-fluorodeoxyglucose. A total of 46 (26.9%) of the tumors had mesenchymal features, and MUC1-Tn positivity was higher in the mesenchymal group than in the epithelial and intermediate groups (P<0.01 and P<0.01, respectively). Patients with tumors exhibiting MUC1-Tn-H had significantly shorter 5-year overall and disease-free survival times (P=0.011 and P<0.001, respectively). Additionally, MUC1-Tn-H was identified as an independent prognostic factor in multivariate analysis (P=0.024). MUC1-Tn is specific for lung cancer cells and can improve diagnostic capabilities. Additionally, it may be a potential therapeutic target in lung ADC.
黏蛋白1(MUC1)在包括肺癌在内的多种癌症中表达上调。然而,传统的抗MUC1抗体由于其特异性有限,对恶性肺肿瘤和良性病变的鉴别并无帮助。我们之前的研究筛选出了一种针对癌症相关糖链结构的新型表位特异性抗体,该抗体可特异性识别MUC1 Tn抗原(MUC1-Tn ED抗体)。在本研究中,检测了其作为肺腺癌(ADC)诊断标志物和治疗工具的潜在效用。使用MUC1-Tn ED抗体(克隆号SN-102)对肺ADC组织芯片进行免疫组织化学分析,并将结果与另一个克隆以及市售MUC1抗体的结果进行比较。分析了SN-102阳性免疫反应性与临床病理因素之间的关联。此外,还分析了MUC1-Tn表达与上皮-间质转化标志物及放射学特征之间的关联。在175例肺ADC病例中,138例(78.9%)观察到中度或高度MUC1-Tn表达(MUC1-Tn-H)。MUC1-Tn-H与男性、吸烟、肿瘤扩展、胸膜侵犯以及术前血清癌胚抗原和细胞角蛋白19片段水平升高相关。根据计算机断层扫描,MUC1-Tn-H的肿瘤具有更高的实变/肿瘤比,且18F-氟脱氧葡萄糖摄取更高。共有46例(26.9%)肿瘤具有间质特征,间质组中MUC1-Tn阳性率高于上皮组和中间组(分别为P<0.01和P<0.01)。表现为MUC1-Tn-H的肿瘤患者的5年总生存期和无病生存期显著缩短(分别为P=0.011和P<0.001)。此外,在多变量分析中,MUC1-Tn-H被确定为独立的预后因素(P=0.024)。MUC1-Tn对肺癌细胞具有特异性,可提高诊断能力。此外,它可能是肺ADC的潜在治疗靶点。