Department of Surgical Oncology and Gynecologic Oncology, "Iuliu Hațieganu" University of Medicine and Pharmacy, 400012 Cluj-Napoca, Romania.
"Prof. Dr. Ion Chiricuță" Institute of Oncology, 400015 Cluj-Napoca, Romania.
Int J Mol Sci. 2024 Jun 9;25(12):6377. doi: 10.3390/ijms25126377.
Since transcription factor Forkhead Box P3 (FoxP3) was identified as a specific regulatory T cell (Treg) marker, researchers have scrutinized its value as a potential novel therapeutic target or a prognostic factor in various types of cancer with inconsistent results. The present analysis was performed to assess the influence of Treg FoxP3 expression on the prognosis of primary melanoma and to evaluate the correlations with various clinicopathological prognostic factors. We analyzed all eligible patients with stage pT3 primary malignant melanomas treated in a tertiary cancer center. Immunohistochemical staining for Treg FoxP3 expression was performed on retrospectively identified paraffin blocks and subsequently correlated with the outcomes of the patients. A total of 81% of the patients presented a positive Treg FoxP3 expression, being correlated with a higher risk of lymph node metastasis, tumor relapse, and death. Moreover, positive expression was statistically associated with a shorter OS. The tumor relapse rate was estimated at 36.7%. A positive expression of Treg FoxP3 and lymph node metastasis were associated with a higher risk of death based on multivariate analysis. Treg FoxP3 expression may be used as an independent prognostic factor in patients with malignant melanoma to evaluate tumor progression and survival.
自从转录因子叉头框 P3(FoxP3)被鉴定为特定的调节性 T 细胞(Treg)标志物以来,研究人员一直在仔细研究其作为各种癌症的潜在新型治疗靶点或预后因素的价值,但结果不一致。本分析旨在评估 Treg FoxP3 表达对原发性黑色素瘤预后的影响,并评估与各种临床病理预后因素的相关性。我们分析了在三级癌症中心治疗的所有符合条件的 pT3 期原发性恶性黑色素瘤患者。对回顾性确定的石蜡块进行 Treg FoxP3 表达的免疫组织化学染色,并随后与患者的结果相关联。81%的患者出现 Treg FoxP3 阳性表达,与淋巴结转移、肿瘤复发和死亡的风险增加相关。此外,阳性表达与 OS 较短具有统计学相关性。肿瘤复发率估计为 36.7%。基于多变量分析,Treg FoxP3 表达和淋巴结转移与死亡风险增加相关。Treg FoxP3 表达可作为评估黑色素瘤患者肿瘤进展和生存的独立预后因素。