文章摘要
食管鳞癌患者血清LCN2 LTBP2表达及其与患者临床病理特征及预后的关系
The expression of serum LCN2 and LTBP2 in patients with esophageal squamous cell carcinoma and their relationship with clinical pathological features and prognosis
投稿时间:2025-05-13  
DOI:10.3969/j.issn.1000-0399.2026.06.008
中文关键词: 食管鳞癌  脂质运载蛋白-2  转化生长因子结合蛋白2  病理特征  预后
英文关键词: Esophageal squamous cell carcinoma  Lipocalin-2  Latent transforming growth factor beta binding protein 2  Pathological features  Prognosis
基金项目:沧州市科学技术局科技计划项目(编号:23244102048)
作者单位
黄明 061000 河北沧州 沧州市人民医院胸外科 
王飞 061000 河北沧州 沧州中西医结合医院消化内科 
李冬 061000 河北沧州 沧州市人民医院胸外科 
潘亚男 061000 河北沧州 沧州市人民医院胸外科 
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中文摘要:
      目的 检测食管鳞癌患者血清脂质运载蛋白-2(LCN2)、转化生长因子结合蛋白2(LTBP2)水平,探究LCN2、LTBP2与患者临床病理特征及预后的关系。方法 回顾性分析2018年4月至2019年12月于沧州市人民医院就诊的食管鳞癌患者110例(患癌组)资料,选择同期来院的健康体检者110例为健康组。收集两组入组时血清样本,记录并比较LCN2、LTBP2水平差异。对患癌组进行为期5年的随访,根据随访结局分为生存组(86例)和死亡组(24例)。采用Cox比例风险回归模型分析患者死亡的影响因素;采用时间依赖性受试者工作特征(ROC)曲线分析血清LCN2、LTBP2对患者死亡的预测价值。采用Kaplan-Meier分析患者的生存曲线。结果 患癌组血清LCN2、LTBP2水平高于健康组(P<0.05)。TNM分期为Ⅲ期、T3~T4浸润深度、低分化程度、有淋巴结转移以及肿瘤大小>5 cm的食管鳞癌患者血清LCN2和LTBP2水平较高(P<0.05)。死亡组血清LCN2、LTBP2较生存组高(P<0.05)。多因素Cox回归(岭回归校正)显示,LCN2和LTBP2升高是食管鳞癌患者死亡的危险因素(P<0.05)。LCN2、LTBP2对食管鳞癌患者死亡有一定的预测价值,二者预测价值随随访时间延长有增加趋势,且二者联合的曲线下面积(AUC)高于LCN2、LTBP2单独预测(P<0.05)。LCN2、LTBP2低表达患者的5年生存率分别高于LCN2、LTBP2高表达患者(P<0.05)。结论 食管鳞癌患者血清LCN2、LTBP2水平升高,与TNM分期、浸润深度、分化程度、淋巴结转移以及肿瘤大小有关,联合血清LCN2、LTBP2可预测患者死亡,且血清LCN2、LTBP2水平较高的患者,其5年生存率较低。
英文摘要:
      Objective To detect the serum lipocalin-2(LCN2) and latent transforming growth factor beta binding protein 2(LTBP2) in patients with esophageal squamous cell carcinoma, and to explore the relationship between LCN2, LTBP2 with the clinical pathological features and prognosis of patients. Methods A prospective study design was employed, enrolling 110 patients with esophageal squamous cell carcinoma who were treated at Cangzhou People,s Hospital between April 2018 and December 2019 as the cancer group. Concurrently, 110 healthy individuals undergoing routine physical examinations were recruited as the healthy control group. Serum samples were collected from both groups at enrollment to measure LCN2 and LTBP2 levels. The cancer group underwent a 5-year follow-up, during which patients were categorized into a survival group(86 cases) and a mortality group(24 cases) based on follow-up outcomes. A Cox proportional hazards regression model was used to analyze the factors associated with patient mortality; time-dependent receiver operating characteristic(ROC) curves were used to assess the predictive value of serum LCN2 and LTBP2 levels for patient mortality. Kaplan-Meier analysis was used to construct survival curves for patients. Results Serum LCN2 and LTBP2 levels were higher in the cancer group than in the healthy group(P<0.05). Esophageal squamous cell carcinoma patients with TNM stage Ⅲ, T3-T4 infiltration depth, low differentiation degree, lymph node metastasis, and tumor size>5 cm had higher serum LCN2 and LTBP2 than patients with TNM stage Ⅰ+Ⅱ, T1-T2 infiltration depth, medium/high differentiation degree, no lymph node metastasis, and tumor size ≤ 5 cm(P<0.05). The death group had higher serum LCN2 and LTBP2 than the survival group(P<0.05). Multivariate Cox regression(adjusted for Ridge regression) showed that elevated LCN2 and LTBP2 levels were risk factors for mortality in patients with esophageal squamous cell carcinoma(P<0.05). LCN2 and LTBP2 had some predictive value for mortality in patients with esophageal squamous cell carcinoma; their predictive value tended to increase with prolonged follow-up, and the AUC of the combined predictor was significantly higher than that of LCN2 or LTBP2 alone(P<0.05). Patients with low LCN2 and LTBP2 had higher 5-year survival rates than those with high LCN2 and LTBP2(P<0.05). Conclusion Serum LCN2 and LTBP2 are elevated in patients with esophageal squamous cell carcinoma, and they are related to TNM staging, infiltration depth, differentiation degree, lymph node metastasis, and tumor size. The joint of serum LCN2 and LTBP2 can predict mortality, and patients with higher serum LCN2 and LTBP2 have lower 5-year survival rates.
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