Department of Otolaryngology, Head and Neck Surgery, The Third Affiliated Hospital of Sun Yat-sen University, No. 600 Tianhe Street, Guangzhou, 510630, Guangdong, China.
Clin Transl Oncol. 2013 Aug;15(8):608-18. doi: 10.1007/s12094-012-0975-z. Epub 2013 Jan 29.
To explore the expression of tumoral Gal-1 in association with clinical parameters and outcome in a large population with laryngeal squamous cell carcinomas (LSCCs).
A total of 187 patients with LSCC were retrospectively enrolled. Immunohistochemistry was performed to evaluate the tumoral expression of Gal-1, apoptosis-related proteins and the density of tumor infiltrating lymphocytes (TILs) in tumor tissues before any intervene. Survival curves were estimated by the Kaplan-Meier method, and differences in survival between groups were determined using the log-rank test. Prognostic effects were evaluated by Cox regression analysis.
A total of 102 carcinomas (54.5 %) were identified as high Gal-1 expression, and 85 carcinomas (45.5 %) as low expression. Tumoral Gal-1 expression was not significantly related with clinical stage and histology differentiation. No correlation of Gal-1 expression with apoptosis-related protein was identified. Instead, Gal-1 status was correlated positively with the ratio of FOXP3(+)/CD8(+) TILs (P = 0.024). In multivariate regression analysis, advanced clinical stage and the presence of metastases were identified as the independent predictors for poor survival in entire cohort. Especially, the statistical correlation between the Gal-1 expression and prognosis was particularly due to the late-stage tumors (P < 0.05).
Current results represent valuable advancements in Gal-1 research and provided further support for using Gal-1 as a diagnostic biomarker and immunotherapeutic target for LSCC.
探讨肿瘤 Gal-1 在大型喉鳞状细胞癌(LSCC)患者中的表达与临床参数及预后的关系。
回顾性纳入 187 例 LSCC 患者。采用免疫组织化学法检测肿瘤组织中 Gal-1 的表达、凋亡相关蛋白及肿瘤浸润淋巴细胞(TILs)密度。采用 Kaplan-Meier 法估计生存曲线,采用对数秩检验比较组间生存差异。采用 Cox 回归分析评估预后效果。
共 102 例(54.5%)癌组织被鉴定为高 Gal-1 表达,85 例(45.5%)为低表达。肿瘤 Gal-1 表达与临床分期和组织学分化无显著相关性。Gal-1 表达与凋亡相关蛋白无相关性。相反,Gal-1 状态与 FOXP3(+)/CD8(+)TILs 比值呈正相关(P=0.024)。多因素回归分析显示,晚期临床分期和转移是整个队列中预后不良的独立预测因素。特别是 Gal-1 表达与预后的统计学相关性主要与晚期肿瘤有关(P<0.05)。
本研究结果代表了 Gal-1 研究的重要进展,并为将 Gal-1 作为 LSCC 的诊断生物标志物和免疫治疗靶点提供了进一步的支持。