肝脏 ›› 2023, Vol. 28 ›› Issue (4): 461-464.

• 肝癌 • 上一篇    下一篇

血清TREM-1、sCD163及sB7-H3检测在原发性肝癌患者中的表达

秦晓平, 张静, 艾平   

  1. 404300 重庆 忠县人民医院肿瘤血液科
  • 收稿日期:2022-08-23 出版日期:2023-04-30 发布日期:2023-08-29
  • 基金资助:
    重庆市科委攻关项目(cstc2018jcyjAX0309)

The expression of TREM-1, sCD163 and sB7-H3 in patients with primary liver cancer

QIN Xiao-ping, ZHANG Jing, AI Ping   

  1. Department of Oncological Hematology, Zhongxian people's Hospital, Chongqing 404300, China
  • Received:2022-08-23 Online:2023-04-30 Published:2023-08-29

摘要: 目的 探讨血清髓样细胞触发受体1(TREM-1)、可溶性CD163分子(sCD163)及可溶性B7-H3(sB7-H3)检测在原发性肝癌患者中的表达。方法 收集2017年5月—2019年5月重庆市忠县人民医院就诊的110例原发性肝癌的临床资料,分为预后不良(死亡,n=45)和预后良好(存活,n=65)两组。比较两组患者基本资料,检测血清TREM-1、sCD163、sB7-H3水平。通过ROC分析血清TREM-1、sCD163、sB7-H3预测原发性肝癌患者预后不良的价值,并进行多因素logistic回归性分析。结果 肿瘤大小≥5 cm、有肝硬化、有血管侵犯的占比及TREM-1、sCD163、sB7-H3水平均为预后不良组高于预后良好组(P<0.05);经ROC和logistic分析,肿瘤大小≥5 cm、有肝硬化、有血管侵犯、TREM-1≥3.625 ng/mL、sCD163≥1.520 μg/mL、sB7-H3≥425.670 pg/mL是原发性肝癌患者预后不良的危险因素(P<0.05)。结论 TREM-1、sCD163及sB7-H3检测在原发性肝癌预后中具有一定预测价值。

关键词: 髓样细胞触发受体1, 可溶性CD163分子, 可溶性B7-H3, 原发性肝癌

Abstract: Objective To explore the expressions of serum myeloid cell trigger receptor 1 (TREM-1), soluble CD163 molecule (sCD163), and soluble B7-H3 (sB7-H3) test in patients with primary liver cancer and their association with the patients' prognosis. Methods The clinical data of 110 cases of primary liver cancer treated in Zhongxian People's Hospital of Chongqing were collected. They were divided into a poor prognosis group (death, N=45) and a good prognosis group (survival, N=65). The basic information and the levels of TREM-1, sCD163 and SB7-H3 of the two groups of patients were detected. The value of serum TREM-1, sCD163 and SB7-H3 in predicting the poor prognosis of HCC patients were analyzed by receiver operating curve (ROC) and multivariate logistic regression analyses. Results The proportion of tumor size ≥5 cm, liver cirrhosis, vascular invasion, and TREM-1, sCD163, and sB7-H3 levels were all higher in the poor prognosis group than those in the good prognosis group (P<0.05). Tumor size≥5 cm, with liver cirrhosis, with vascular invasion, TREM-1≥3.625 ng/mL, sCD163≥1.520 μg/mL, and sB7-H3≥425.670 pg/mL were the risk factors for poor prognosis in primary HCC patients (P<0.05). Conclusion TREM-1, sCD163, and sB7-H3 tests may have value in predicting the prognosis of primary liver cancer.

Key words: Myeloid cells trigger receptor 1, Soluble CD163 molecule, Soluble B7-H3, Primary liver cancer