Li Huigang, Lin Zuyuan, Zhuo Jianyong, Yang Modan, Shen Wei, Hu Zhihang, Ding Yichen, Chen Hao, He Chiyu, Yang Xinyu, Dong Siyi, Wei Xuyong, Sun Beicheng, Zheng Shusen, Lang Ren, Lu Di, Xu Xiao
Zhejiang University School of Medicine, Hangzhou 310058, China.
Key Laboratory of Integrated Oncology and Intelligent Medicine of Zhejiang Province, Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou 310006, China.
Chin J Cancer Res. 2023 Feb 28;35(1):66-80. doi: 10.21147/j.issn.1000-9604.2023.01.07.
Lung metastasis is a common and fatal complication of liver transplantation for hepatocellular carcinoma (HCC). The precise prediction of post-transplant lung metastasis in the early phase is of great value.
The mRNA profiles of primary and paired lung metastatic lesions were analyzed to determine key signaling pathways. We enrolled 241 HCC patients who underwent liver transplantation from three centers. Tissue microarrays were used to evaluate the prognostic capacity of tumor necrosis factor (TNF), tumor necrosis factor receptor 1 (TNFR1), and TNFR2, particularly for post-transplant lung metastasis.
Comparison of primary and lung metastatic lesions revealed that the TNF-dependent signaling pathway was related to lung metastasis of HCC. The expression of TNF was degraded in comparison to that in para-tumor tissues (P<0.001). The expression of key receptors in the TNF-dependent signaling pathway, TNFR1 and TNFR2, was higher in HCC tissues than in para-tumor tissues (P<0.001). TNF and TNFR1 showed no relationship with patients' outcomes, whereas elevated TNFR2 in tumor tissue was significantly associated with worse overall survival (OS) and increased recurrence risk (5-year OS rate: 31.9% 62.5%, P<0.001). Notably, elevated TNFR2 levels were also associated with an increased risk of post-transplant lung metastasis (hazard ratio: 1.146; P<0.001). Cox regression analysis revealed that TNFR2, Hangzhou criteria, age, and hepatitis B surface antigen were independent risk factors for post-transplant lung metastasis, and a novel nomogram was established accordingly. The nomogram achieved excellent prognostic efficiency (area under time-dependent receiver operating characteristic =0.755, concordance-index =0.779) and was superior to conventional models, such as the Milan criteria.
TNFR2 is a potent prognostic biomarker for predicting post-transplant lung metastasis in patients with HCC. A nomogram incorporating TNFR2 deserves to be a helpful prognostic tool in liver transplantation for HCC.
肺转移是肝细胞癌(HCC)肝移植常见且致命的并发症。早期精确预测移植后肺转移具有重要价值。
分析原发性和配对肺转移病灶的mRNA谱,以确定关键信号通路。我们纳入了来自三个中心接受肝移植的241例HCC患者。使用组织微阵列评估肿瘤坏死因子(TNF)、肿瘤坏死因子受体1(TNFR1)和TNFR2的预后能力,特别是对移植后肺转移的预后能力。
原发性和肺转移病灶的比较显示,TNF依赖性信号通路与HCC的肺转移有关。与癌旁组织相比,TNF的表达降低(P<0.001)。TNF依赖性信号通路中的关键受体TNFR1和TNFR2在HCC组织中的表达高于癌旁组织(P<0.001)。TNF和TNFR1与患者预后无关,而肿瘤组织中TNFR2升高与总体生存率较差和复发风险增加显著相关(5年总生存率:31.9%对62.5%,P<0.001)。值得注意的是,TNFR2水平升高也与移植后肺转移风险增加相关(风险比:1.146;P<0.001)。Cox回归分析显示,TNFR2、杭州标准、年龄和乙肝表面抗原是移植后肺转移的独立危险因素,并据此建立了新的列线图。该列线图具有出色的预后效率(时间依赖性受试者工作特征曲线下面积=0.755,一致性指数=0.779),且优于传统模型,如米兰标准。
TNFR2是预测HCC患者移植后肺转移的有效预后生物标志物。纳入TNFR2的列线图值得成为HCC肝移植中有用的预后工具。