Li Yazhao, Wang Haoyu, Ren Danfeng, Li Jingyu, Mu Zihan, Li Chaoyi, He Yongchao, Zhang Jiayi, Fan Rui, Yin Jiayuan, Su Jiaojiao, He Yinli, Yao Bowen
Center for Translational Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Zonglian College, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Front Oncol. 2024 May 21;14:1408584. doi: 10.3389/fonc.2024.1408584. eCollection 2024.
For the lack of effective serum markers for hepatocellular carcinoma(HCC) diagnosis, it is difficult to detect liver cancer and identify its recurrence early.
Databases were used to analyze the genes potentially associated with alpha-fetoprotein(AFP). ELISA assay was used to detect the serum IL-41 in HCC, liver metastases, hepatitis, and healthy people. Immunohistochemical staining was used to analyze the relative quantification of IL-41 in HCC and paracancer tissues. Various survival curves were plotted according to clinical pathological data and helped us draw the ROC curve of IL-41 diagnosis of HCC.
The serum expression of IL-41 was highest in AFP negative HCC patients and significantly higher than that in AFP positive HCC and metastatic cancer patients. There was a significant negative correlation between elevated serum IL-41 and AFP(<1500ng/ml). The clinicopathological features suggested that the serum IL-41 level was significantly correlated with capsule invasion, low differentiation and AFP. High serum expression of IL-41 suggests poorer survival and earlier recurrence after resection, and IL-41 upregulated in patients with early recurrence and death. The expression of IL-41 was higher in HCC tissues of patients with multiple tumors or microvascular invasion. The ROC curve showed that serum IL-41 had a sensitivity of 90.17 for HCC and a sensitivity of 96.63 for AFP-negative HCC, while the specificity was higher than 61%.
IL-41 in serum and tissue suggests poor prognosis and postoperative recurrence in HCC patients and could be a new serum diagnostic marker for AFP negative patients.
由于缺乏用于肝细胞癌(HCC)诊断的有效血清标志物,肝癌的早期检测及复发识别存在困难。
利用数据库分析与甲胎蛋白(AFP)潜在相关的基因。采用酶联免疫吸附测定(ELISA)法检测HCC、肝转移癌、肝炎患者及健康人的血清白细胞介素-41(IL-41)。采用免疫组织化学染色分析HCC及癌旁组织中IL-41的相对定量。根据临床病理数据绘制各种生存曲线,并绘制IL-41诊断HCC的ROC曲线。
IL-41血清表达在AFP阴性HCC患者中最高,显著高于AFP阳性HCC及转移癌患者。血清IL-41升高与AFP(<1500ng/ml)之间存在显著负相关。临床病理特征表明,血清IL-41水平与包膜侵犯、低分化及AFP显著相关。血清IL-41高表达提示切除术后生存较差且复发较早,早期复发及死亡患者中IL-41上调。多肿瘤或微血管侵犯患者的HCC组织中IL-41表达较高。ROC曲线显示,血清IL-41对HCC的敏感性为90.17,对AFP阴性HCC的敏感性为96.63,而特异性高于61%。
血清及组织中的IL-41提示HCC患者预后不良及术后复发,可能成为AFP阴性患者的新型血清诊断标志物。