Rosu Mihai Catalin, Tarta Cristi, Moldovan Silviu, Neamtu Andreea-Adriana, Ardelean Andrei, Capitanio Marco, Herczeg Diana, Faur Ionut-Flaviu, Bende Renata, Pilat Luminita, Prunoiu Virgiliu Mihai, Neamtu Carmen, Totolici Bogdan Dan
Surgery Department, Clinical County Emergency Hospital of Arad, Andrenyi Karoly Str., No. 2-4, 310037 Arad, Romania.
Faculty of Medicine, "Vasile Goldis" Western University of Arad, Liviu Rebreanu Str., Nr. 86, 310045 Arad, Romania.
Biomedicines. 2025 Apr 9;13(4):928. doi: 10.3390/biomedicines13040928.
: Gastric cancer remains a leading cause of cancer mortality worldwide. Reliable biomarkers are crucial for early detection, prognostication, and therapy monitoring. While classical tumor markers such as carcinoembryonic antigen (CEA), cancer antigen (CA)19-9, CA72-4, and alpha-fetoprotein (AFP) are used in clinical practice, their accuracy can be limited. Tumor necrosis factor alpha (TNF-α) is an inflammatory cytokine implicated in tumor progression, yet its relationship with established gastric cancer tumor markers has not been fully clarified. This study aimed to determine whether elevated TNF-α correlates with key tumor markers and disease stage in gastric cancer. : In this prospective observational study, we enrolled 80 gastric cancer patients and 20 non-neoplastic controls. Baseline clinical data, laboratory parameters, and tumor markers (CEA, CA19-9, CA72-4, AFP) were recorded. TNF-α concentrations were measured using enzyme-linked immunosorbent assays. Correlation analyses and multivariate regression were performed to assess the relationship of TNF-α with tumor markers, inflammatory indices, and disease stage. : TNF-α was significantly elevated in gastric cancer patients (median 4.5 pg/mL) compared to controls (2.9 pg/mL). TNF-α showed a robust correlation with CA19-9 (rho = 0.502) and CA72-4 (rho = 0.385), and a moderate correlation with CEA (rho = 0.279). TNF-α concentrations were highest in Stage IV disease and in the intestinal-type histology. In regression analysis, only CA19-9 and CA72-4 remained independent predictors of TNF-α after controlling for clinical confounders. : TNF-α is strongly associated with CA19-9 and CA72-4 and rises with advancing stage, highlighting its potential as an adjunct marker for assessing gastric cancer burden. These findings provide a rationale for further research on TNF-α as both a prognostic biomarker and a possible therapeutic target in gastric cancer.
胃癌仍是全球癌症死亡的主要原因。可靠的生物标志物对于早期检测、预后评估和治疗监测至关重要。虽然癌胚抗原(CEA)、癌抗原(CA)19-9、CA72-4和甲胎蛋白(AFP)等经典肿瘤标志物已应用于临床实践,但其准确性可能有限。肿瘤坏死因子α(TNF-α)是一种与肿瘤进展相关的炎性细胞因子,然而其与已确定的胃癌肿瘤标志物之间的关系尚未完全阐明。本研究旨在确定TNF-α升高是否与胃癌的关键肿瘤标志物及疾病分期相关。
在这项前瞻性观察研究中,我们纳入了80例胃癌患者和20例非肿瘤对照。记录基线临床数据、实验室参数及肿瘤标志物(CEA、CA19-9、CA72-4、AFP)。采用酶联免疫吸附测定法测量TNF-α浓度。进行相关性分析和多变量回归以评估TNF-α与肿瘤标志物、炎症指标及疾病分期之间的关系。
与对照组(2.9 pg/mL)相比,胃癌患者的TNF-α显著升高(中位数为4.5 pg/mL)。TNF-α与CA19-9(rho = 0.502)和CA72-4(rho = 0.385)呈强相关性,与CEA呈中度相关性(rho = 0.279)。TNF-α浓度在IV期疾病及肠型组织学中最高。在回归分析中,控制临床混杂因素后,仅CA19-9和CA72-4仍是TNF-α的独立预测因子。
TNF-α与CA19-9和CA72-4密切相关,并随疾病分期进展而升高,凸显了其作为评估胃癌负担辅助标志物的潜力。这些发现为进一步研究TNF-α作为胃癌的预后生物标志物和可能的治疗靶点提供了理论依据。