肝脏 ›› 2022, Vol. 27 ›› Issue (12): 1288-1291.

• 肝癌 • 上一篇    下一篇

肝细胞癌患者血清SLC7A11的变化及临床意义

詹有芳, 张珏, 王鹏   

  1. 200021 上海中医药大学附属曙光医院检验科(詹有芳,张珏);上海市第七人民医院检验科(王鹏)
  • 收稿日期:2022-01-02 发布日期:2023-01-30
  • 通讯作者: 王鹏,Email:wanghahapeng@sina.cn
  • 基金资助:
    上海市卫生健康委员会面上项目(201740318)

Changes and clinical significance of serum SLC7A11 in patients with hepatocellular carcinoma

ZHAN You-fang1, ZHANG Jue1, WANG Peng2△   

  1. 1. Department of Clinal Lab, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medine, Shanghai 200021, China;
    2. Department of Clinal Lab, the Seven People’s Hospital of Shanghai, Shanghai 200137, China
  • Received:2022-01-02 Published:2023-01-30
  • Contact: WANG Peng,Email:wanghahapeng@sina.cn

摘要: 目的 观察肝细胞癌(HCC)患者SLC7A11的变化及其临床意义。方法 收集2018年1月—2020年12月上海中医药大学附属曙光医院收治的120例HCC患者(HCC组),另选取肝硬化患者78例(LC组)。120例HCC患者中早期HCC患者60例,晚期HCC患者60例。检测所有研究对象的TBil、ALT、PT、Alb、AFP及SLC7A11水平,观察HCC患者TBil、ALT、PT、Alb、AFP及SLC7A11水平,以及AFP、SLC7A11及AFP联合SLC7A11的ROC曲线的诊断评价。计量资料组间比较采用独立样本t检验,计数资料组间比较采用χ2检验,诊断评价采用ROC曲线分析。结果 早期HCC患者血清TBil、PT水平明显低于晚期HCC组(t值分别为-5.015,-6.068,P均<0.01),Alb则高于晚期HCC组(t值为3.503,P<0.01),早期HCC患者血清 SLC7A11低于晚期HCC组[(55.71±18.98) ng/mL vs (65.31±22.31) ng/mL, t=-2.538, P<0.05]; 早期HCC患者血清TBil、PT明显低于LC组(t分别为2.999, 4.687, P均<0.01),SLC7A11、AFP、Alb则明显高于LC组[SLC7A11: (55.71±18.98) ng/mL vs (37.38±19.98) ng/mL, t=-5.462, P<0.01; AFP (673.58±587.90) vs (147.87±95.05), t=-7.775, P<0.01; Alb: (35.71±3.83) ng/mL vs (32.10±5.52) ng/ mL, t=-4.333, P<0.01];单独SLC7A11与AFP诊断HCC无明显差异(AUC分别为0.792, 0.801),但联合检测(AUC为0.869)明显高于单项检测; 单独 SLC7A11与AFP诊断早期HCC无明显差异(AUC分别为0.752, 0.765),但联合检测(AUC为0.802)明显高于单项检测。结论 血清SLC7A11在诊断早期HCC中具有一定的临床应用价值,特别是和AFP联合检测时。

关键词: 肝细胞癌, SLC7A11, 甲胎蛋白, 肿瘤标志物

Abstract: Objective To investigate the clinical significance of serum SLC7A11 in patients with hepatocellular carcinoma (HCC).Methods A total of 120 patients with HCC admitted to our hospital from January 2018 to December 2020 were enrolled as HCC group, and 78 liver cirrhosis persons (LC) who underwent physical examination were enrolled as control group. Among the 120 patients in the HCC group, 60 were the early stage HCC and 60 were advanced HCC. Clinical data of all patients including serume levels of total bilirubin (TBil), alanine aminotransferase (ALT), prothrombin time (PT), albumin (Alb), alpha-fetoprotein (AFP), and SLC7A11 were collected. The TBil, ALT, PT, Alb, AFP and SLC7A11 levels of HCC patients were analyzed. The diagnostic values of AFP, SLC7A11 and AFP combined with SLC7A11 were analyzed. Continuous data was compared by independent samples t-test, categorical data was analyzed by chi-square test. The ROC curve analysis was used for diagnostic evaluation.Results The serum levels of TBil and PT in the early stage HCC group were significantly lower than those in the advanced HCC group (t=-5.015 and -6.068, all P<0.01),and the level of Alb in the early stage HCC group was significantly higher than that of the advanced HCC group (t=-3.503, P<0,01). The serum SLC7A11 of patients with early stage HCC was lower than that of patients with advanced HCC [(55.71 ± 18.98) ng/mL vs (65.31 ± 22.31) ng/mL, t=-2.538, P<0.05]. The serum TBil and PT of patients in the early stage HCC group were significantly lower than those of LC group (t=2.999 and 4.687, all P<0.01). The serum SLC7A11, AFP and Alb of patients in the early stage HCC group were significantly higher than that of patients in LC group [SLC7A11: (55.71 ± 18.98) ng/mL vs (37.38 ± 19.98) ng/mL, t=-5.462, P<0.01; AFP (673.58 ± 587.90) vs (147.87 ± 95.05), t=-7.775, P<0.01; Alb (35.71 ± 3.83) ng/mL vs (32.10 ± 5.52) ng/ mL, t=-4.333, P<0.01]. There was no significant difference between SLC7A11 and AFP in the diagnosis of HCC (AUC 0.792 and 0.801, respectively), but the combined test (AUC 0.869) was significantly higher than the single test. There was no significant difference between SLC7A11 and AFP alone in the diagnosis of early stage HCC (AUC 0.752 and 0.765, respectively), but the combined detection (AUC 0.802) was significantly higher than that of single detection.Conclusion The serum SLC7A11 has certain clinical value in the diagnosis of early HCC, especially combined with AFP.

Key words: Hepatocellular carcinoma, SLC7A11, Alpha-fetoprotein, Tumor marker