Kim Gilhyang, Lee Kyung-Jun, Shin Eun, Park Sung Taek, Kim Hyeong Su, Cho Hye-Yon
Department of Pathology, Kangnam Sacred-Heart Hospital, Hallym University Medical Center, Hallym University College of Medicine, Seoul 07441, Republic of Korea.
Department of Pathology, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul 03181, Republic of Korea.
Int J Mol Sci. 2025 Mar 17;26(6):2687. doi: 10.3390/ijms26062687.
CT83, a cancer-testis antigen, has emerged as a potential biomarker and therapeutic target in various cancers. This study explores its expression and role in cervical adenocarcinoma progression and prognosis. CT83 expression was analyzed in cervical cancer cell lines using quantitative PCR and Western blotting. Functional assays demonstrated that CT83 overexpression (OE) promotes proliferation, migration, invasion, and epithelial-mesenchymal transition (EMT) in cervical cancer cells while also upregulating PD-L1 expression. Conversely, CT83 knockdown reduced these malignant phenotypes. The immunohistochemical analysis of 60 patient samples revealed CT83 expression in 84.9% of cases, with significant correlations to larger tumor size, elevated squamous cell carcinoma antigen (SCC) levels, and advanced FIGO stages (II-IV). Furthermore, intermediate-to-high CT83 expression (H-score ≥100) was associated with more aggressive disease features. These findings suggest that CT83 contributes to tumor progression and immune evasion, likely through PD-L1 modulation. As a highly expressed antigen in cervical adenocarcinoma, CT83 offers promise as a diagnostic marker and therapeutic target for improving patient outcomes.
CT83是一种癌睾丸抗原,已成为多种癌症中潜在的生物标志物和治疗靶点。本研究探讨其在宫颈腺癌进展和预后中的表达及作用。采用定量PCR和蛋白质免疫印迹法分析了宫颈癌细胞系中CT83的表达。功能试验表明,CT83过表达(OE)促进宫颈癌细胞的增殖、迁移、侵袭和上皮-间质转化(EMT),同时上调PD-L1表达。相反,CT83基因敲低可减少这些恶性表型。对60例患者样本的免疫组织化学分析显示,84.9%的病例中有CT83表达,与更大的肿瘤大小、升高的鳞状细胞癌抗原(SCC)水平和较高的国际妇产科联盟(FIGO)分期(II-IV期)显著相关。此外,中至高度CT83表达(H评分≥100)与更具侵袭性的疾病特征相关。这些发现表明,CT83可能通过调节PD-L1促进肿瘤进展和免疫逃逸。作为宫颈腺癌中高表达的抗原,CT83有望成为改善患者预后的诊断标志物和治疗靶点。