中国实用口腔科杂志 ›› 2025, Vol. 18 ›› Issue (6): 723-730.DOI: 10.19538/j.kq.2025.06.013

• 论著 • 上一篇    下一篇

外生骨疣蛋白2在头颈部鳞状细胞癌中的突变、表达特征及对预后影响初探

郑丹童,王    洋,刘松淼,刘小舟   

  1. 中国医科大学附属口腔医院医疗保健中心,辽宁省口腔医学研究所,辽宁 沈阳 110012
  • 出版日期:2025-11-30 发布日期:2025-11-30
  • 通讯作者: 刘小舟
  • 基金资助:
    辽宁省科学技术计划项目(2023JH2/101300016)

  • Online:2025-11-30 Published:2025-11-30

摘要: 目的    初步探索外生骨疣蛋白2(exostosin glycosyltransferase 2,EXT2)在头颈部鳞状细胞癌(head and neck squamous cell carcinoma,HNSCC)中的突变和表达特征,以及对临床预后的影响。方法    选取2015年1月至2024年1月于中国医科大学附属口腔医院采用下一代测序技术检测的HNSCC患者20例,以≥ 2例病例检出的突变基因作为目标基因在癌症基因组图谱(the cancer genome atlas,TCGA)数据库中进行分析。采用RNA测序技术检测20例HNSCC患者肿瘤组织中EXT2的相对表达量,将其分为EXT2高表达组(相对表达量>中位数)和EXT2低表达组(相对表达量≤中位数),比较分析2组患者预后情况。在TCGA公共数据库中,比较503例HNSCC患者肿瘤组织与癌旁正常组织中目标基因的表达差异及对预后的影响;采用单样本基因集富集分析算法计算24类免疫细胞在HNSCC肿瘤微环境中的浸润评分及其与EXT2表达的相关性;分析EXT2的表达对33种肿瘤预后的影响。结果    20例HNSCC患者中有11例检测出基因突变,累计突变基因62个,≥ 2例病例检出的突变基因(目标基因)13个。其中,EXT2在2例男性Ⅳ期低分化患者中检测出点突变。EXT2突变对患者无进展生存期具有显著影响(χ2 = 15.000,P < 0.001)。EXT2高表达组无进展生存期显著短于低表达组,差异有统计学意义(χ2 = 9.210,P = 0.002)。基于TCGA数据库分析显示,在目标基因中,EXT2、BRCA1相关蛋白1、FAT非典型钙黏蛋白1、圆柱瘤病蛋白、Janus激酶1、减数分裂重组11同源物、核因子κB抑制剂α、ROS原癌基因1、隔膜蛋白9在肿瘤组织中的相对表达量高于癌旁正常组织,差异有统计学意义(P < 0.05)。其中,仅EXT2高表达是患者预后的危险因素(HR = 1.444,95%CI:1.104 ~ 1.890,P = 0.007)。在HNSCC肿瘤微环境中,EXT2高表达与巨噬细胞、中性粒细胞及自然杀伤细胞等浸润评分呈正相关,与B细胞、CD8+ T细胞及细胞毒性细胞等浸润评分呈负相关(均P < 0.05)。EXT2高表达是HNSCC、膀胱尿路上皮癌、脑低级别胶质瘤、肝细胞癌、间皮瘤及肉瘤患者预后的危险因素(均HR > 1.000,P < 0.05)。结论    EXT2突变及表达情况与HNSCC的预后密切相关,其可能通过重塑免疫抑制微环境影响多种肿瘤的发展,并有潜力成为预测HNSCC预后的生物标志物。

关键词: 头颈部鳞状细胞癌, 外生骨疣蛋白2, 突变, 预后

Abstract: Objective    To preliminarily explore the gene mutation and expression characteristics of exostosin glycosyltransferase 2(EXT2)in head and neck squamous cell carcinoma(HNSCC)and its impact on clinical prognosis. Methods    A total of 20 HNSCC patients who underwent next-generation sequencing at the Stomatological Hospital Affiliated to China Medical University from January 2015 to January 2024 were selected. Mutant genes detected in ≥ 2 cases were regarded as target genes for analysis in the cancer genome atlas(TCGA)database. RNA-seq was used to detect the relative expression level of EXT2 in tumor tissues of 20 HNSCC patients. The patients were divided into the EXT2 high-expression group(relative expression level > median)and the EXT2 low-expression group(relative expression level ≤ median),and the prognosis of the two groups was compared and analyzed. In the TCGA public database,the expression difference of target genes between tumor tissues and adjacent normal tissues of 503 HNSCC patients and its impact on prognosis were compared. The single-sample gene set enrichment analysis algorithm was used to calculate the infiltration scores of 24 types of immune cells in the HNSCC tumor microenvironment and their correlation with EXT2 expression. The impact of EXT2 expression on the prognosis of 33 types of tumors was analyzed. Results    Among the 20 HNSCC patients,gene mutations were detected in 11 cases,with a total of 62 mutant genes,including 13 target genes(mutant genes detected in ≥ 2 cases). Among them,point mutations in the EXT2 gene were detected in 2 male patients with stage Ⅳ poorly differentiated HNSCC. EXT2 gene mutation had a significant impact on the progression-free survival of patients(χ2 = 15.000,P < 0.001). The progression-free survival of the EXT2 high-expression group was significantly shorter than that of the low-expression group,and the difference was statistically significant(χ2 = 9.210,P = 0.002). Analysis based on the TCGA database showed that among the target genes,the relative expression levels of EXT2,BRCA1- associated protein 1(BAP1),FAT atypical cadherin 1(FAT1),cylindromatosis protein(CYLD),Janus kinase 1(JAK1),meiotic recombination 11 homolog(MRE11),nuclear factor kappa-B inhibitor alpha(NFKBIA),ROS proto-oncogene 1(ROS1),and septin 9(SEPTIN9)in tumor tissues were higher than those in adjacent normal tissues,and the differences were statistically significant(all P < 0.05). Among them,only high EXT2 expression was a risk factor for patient prognosis(HR = 1.444,95%CI:1.104 - 1.890,P = 0.007). In the HNSCC tumor microenvironment,high EXT2 expression was positively correlated with the infiltration scores of macrophages,neutrophils,and natural killer cells,and negatively correlated with the infiltration scores of B cells,CD8+ T cells,and cytotoxic cells(all P < 0.05). High EXT2 expression was a risk factor for the prognosis of patients with HNSCC,bladder urothelial carcinoma,low-grade glioma of head,hepatocellular carcinoma,mesothelioma,and sarcoma(all HR > 1.000,P < 0.05). Conclusion    EXT2 gene mutation and expression are closely related to the prognosis of HNSCC. It may affect the development of various tumors by remodeling the immunosuppressive microenvironment and has the potential to be a biomarker for predicting the prognosis of HNSCC.

Key words: head and neck squamous cell carcinoma, HNSCC;exostosin glycosyltransferase 2, EXT2;mutation;prognosis

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