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中国临床研究:2024,37(9):1369-1373
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结直肠癌组织M2型肿瘤相关巨噬细胞预测淋巴结转移的风险
(荆门市中心医院 荆楚理工学院附属中心医院结直肠肛门外科,湖北 荆门 448001)
Prediction of lymph node metastasis risk by M2 tumor associated macrophages in colorectal cancer tissue
(Department of Colorectal and Anal Surgery, Affiliated Central Hospital of Jingchu University of Technology, Jingmen Central Hospital, Jingmen, Hubei 448001, China)
摘要
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投稿时间:2024-07-17   网络发布日期:2024-09-21
中文摘要: 目的 基于结直肠癌(CRC)组织M2型肿瘤相关巨噬细胞活性生物标志物可溶性CD163蛋白(sCD163)探讨淋巴结转移(LNM)的风险。方法 回顾性分析2018年1月至2019年5月在荆门市中心医院接受初次手术治疗的152例CRC患者和58例结直肠腺瘤患者的临床资料和术前血清学标志物水平。手术前一天收集血液标本,使用酶联免疫吸附试验(ELISA)测量血清样本中sCD163、癌胚抗原(CEA)、糖类抗原(CA)199水平。术后对患者进行随访,随访截止时间是2024年4月30日。记录患者的总生存期和无病生存期。结果 无LNM患者sCD163水平明显低于有LNM患者[(2.79±0.76)mg/L? vs (4.25±1.50)mg/L, t=7.958, P<0.01]。多因素logistic回归分析显示,sCD163>3.50 mg/L是CRC患者LNM的独立影响因素(HR=13.973, 95%CI: 5.385~36.259, P<0.05)。sCD163>3.50 mg/L预测CRC患者LNM的效能最高(曲线下面积为0.742,灵敏度为68.8%,特异度为79.7%)。sCD163>3.50 mg/L组患者中35例(46.1%)死亡,sCD163≤3.50 mg/L患者中12例(15.8%)死亡,两组总生存期比较差异有统计学意义(log-rank χ2=15.583, P<0.01);sCD163>3.50 mg/L组患者中42例(55.3%)复发,sCD163≤3.50 mg/L患者中25例(32.9%)复发,两组无复发生存期比较差异有统计学意义(log-rank χ2=8.368, P=0.004)。结论 反映组织中M2巨噬细胞活性的生物标志物sCD163水平升高与CRC患者的LNM和不良预后显著相关,并且sCD163可能是确定LNM高风险CRC患者的潜在预测因子。
Abstract:Objective To investigate the risk of lymph node metastasis (LNM) in colorectal cancer (CRC) based on the M2 macrophage activity biomarker soluble CD163 (sCD163). Methods The clinical data and preoperative blood samples of 152 patients with CRC and 58 patients with colorectal adenoma who received primary surgery in Jingmen Central Hospital from January 2018 to May 2019 were collected. Blood samples were collected the day before surgery, and enzyme-linked immunosorbent assay (ELISA) was used to measure serum levels of sCD163, carcinoembryonic antigen (CEA), and carbohydrate antigen 199 (CA199). Postoperative follow-up was conducted with a cutoff date of April 30, 2024, and the overall survival and disease-free survival were recorded. Results The level of sCD163 in patients without LNM was significantly lower than in those with LNM [(2.79±0.76) mg/L? vs (4.25±1.50) mg/L, t=7.958, P<0.01]. Multivariate logistic regression analysis indicated that sCD163>3.50 mg/L was an independent risk factor for LNM in CRC patients (HR=13.973, 95%CI: 5.385-36.259, P<0.05). sCD163>3.50 mg/L had the highest ability to predict lymph node metastasis in CRC patients (AUC=0.742), with a sensitivity of 68.8% and a specificity of 79.7%. There were 35 patients (46.1%) died in the group of sCD163>3.50 mg/L, and 12 patients (15.8%) died in the group of sCD163≤3.50 mg/L. There was a significant difference in overall survival between the two groups (log-rank χ2=15.583, P<0.01). There were 42 patients (55.3%) in the group of sCD163>3.50 mg/L relapsed, and 25 patients (32.9%) in the group of sCD163≤3.50 mg/L relapsed. The difference in recurrence-free survival between the two groups was statistically significant (log-rank χ2=8.368, P=0.004). Conclusion Elevated levels of the biomarker sCD163, which reflects M2 macrophage activity in tissues, are significantly associated with LNM and poor prognosis in CRC patients, and sCD163 may be a potential predictive factor for identifying CRC patients at high risk of LNM.
文章编号:     中图分类号:R735.3    文献标志码:A
基金项目:湖北省卫生健康科研基金项目(WJ2019M074);荆门市科学技术研究与开发计划(2023YDKY030)
引用文本:
朱小玄,龙舟,曹少华.结直肠癌组织M2型肿瘤相关巨噬细胞预测淋巴结转移的风险[J].中国临床研究,2024,37(9):1369-1373.

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