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趋化因子CXCL5和程序性死亡配体 1在结肠直肠癌组织的表达与病人预后的关系

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  • 上海交通大学医学院附属瑞金医院外科 上海市微创外科临床医学中心,上海 200025

收稿日期: 2020-05-09

  网络出版日期: 2022-07-27

基金资助

国家自然科学基金(81871933);国家自然科学基金青年基金(81802326)

Expression of chemokine CXCL5 and programme death ligand 1 in colorectal cancer tissues are associated with prognosis of patients

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  • Department of Surgery, Ruijin Hospital, Shanghai JiaoTong University School of Medicine,Shanghai Minimally Invasive Surgery Center, Shanghai 200025, China

Received date: 2020-05-09

  Online published: 2022-07-27

摘要

目的:分析CXCL5(C-X-C motif ligand 5)蛋白与程序性死亡配体1(programmed death ligand 1,PD-L1)在结肠直肠癌组织中的表达,并探讨两者与临床特征的关系及预后价值。方法:收集2010年至2011年行腹腔镜切除手术的结肠直肠癌病人肿瘤组织及癌旁正常组织标本,共78例。同时对所有病例进行临床资料收集及预后随访。标本制备组织芯片,行免疫组织化学染色。采用免疫危险评分标准对CXCL5、PD-L1表达进行评分,分析其表达与各项临床病理参数关系。最后分析CXCL5、PD-L1表达与结肠直肠癌病人预后的关系。结果:结肠直肠癌组织中CXCL5、PD-L1表达均高于癌旁正常组织,与肿瘤直径、TNM分期相关。Cox单因素回归分析显示,TNM分期、CXCL5高表达、PD-L1高表达是结肠直肠癌病人总生存率的预后危险因素。多因素回归分析显示,TNM分期和PD-L1高表达是结肠直肠癌病人总生存率的独立预后危险因素。CXCL5与PD-L1均高表达的病人预后最差。结论:CXCL5与PD-L1联合可对结肠直肠癌病人进行危险度分层,预测病人预后。

本文引用格式

刘诗光, 赵敬坤, 陆爱国, 毛志海 . 趋化因子CXCL5和程序性死亡配体 1在结肠直肠癌组织的表达与病人预后的关系[J]. 外科理论与实践, 2021 , 26(06) : 543 -549 . DOI: 10.16139/j.1007-9610.2021.06.017

Abstract

Objective To analyze the expression of CXCL5 (C-X-C motif ligand 5) and programme death ligand 1 (PD-L1) in colorectal cancer tissues and explore two chemokines associated with clinical characteristics and prognosis. Methods The specimens of tumor tissues and adjacent normal tissues were collected from 78 patients with colorectal cancer who had laparoscopic resection from 2010 to 2011. The clinical data were gotten and follow-up were done for prognosis. Tissue microarrays were made from all specimens and immunohistochemical staining was performed. Expression of CXCL5 and PD-L1 was evaluated using immune risk scoring and analyzed with the association of clinical pathological parameters and prognosis of patients. Results Expression of CXCL5 and PD-L1 was associated with tumor size and TNM stage, and was higher in colorectal cancer tissues than in adjacent normal tissues. Cox univariate regression analysis showed that TNM stage, high expression of both CXCL5 and PD-L1 were the prognostic risk factors for overall survival of colorectal patients. It was shown with multivariate regression analysis that TNM stage and high expression of PD-L1 were the independent prognostic risk factors for overall survival rate. Patients with higher expression of both CXCL5 and PD-L1 had the worst prognosis. Conclusions CXCL5 combined with PD-L1 could stratify the risk of patients with colorectal cancer and predict the prognosis of patients.

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