癌变·畸变·突变 ›› 2025, Vol. 37 ›› Issue (3): 190-195.doi: 10.3969/j.issn.1004-616x.2025.03.003

• 论著 • 上一篇    

RUNX家族转录因子1在宫颈腺癌组织中的表达水平及其与患者预后的关系

郭艾, 黄宁, 张菁, 张媛媛, 安菊生, 刘梅   

  1. 国家癌症中心/国家肿瘤临床医学研究中心/中国医学科学院北京协和医学院肿瘤医院, 分子肿瘤学全国重点实验室, 北京 100021
  • 收稿日期:2024-12-23 修回日期:2025-03-10 发布日期:2025-06-13
  • 通讯作者: 刘梅
  • 作者简介:郭艾,E-mail:guoai0522@163.com。
  • 基金资助:
    中国医学科学院医学与健康科技创新工程(2021-I2M-1-018)

Expression of RUNX family transcription factor 1 and its prognostic value in cervical adenocarcinomas

GUO Ai, HUANG Ning, ZHANG Jing, ZHANG Yuanyuan, AN Jusheng, LIU Mei   

  1. State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China
  • Received:2024-12-23 Revised:2025-03-10 Published:2025-06-13

摘要: 目的:宫颈腺癌以其高侵袭性而显著不同于宫颈鳞状细胞癌,且对放疗的响应较低,导致患者预后不良和生存率较低。本研究旨在探讨RUNX家族转录因子1(RUNX1)在宫颈腺癌组织中的表达水平及其与患者预后的关系。方法:收集37例宫颈腺癌患者的肿瘤组织样本,通过免疫组织化学法检测肿瘤组织中RUNX1的表达水平,统计分析其表达水平与患者病理指标以及预后的相关性。利用人类蛋白质图谱(HPA)数据库分析RUNX1在宫颈腺癌组织中的蛋白表达水平。利用GSVA评分和TIMER2.0平台对癌症基因组图谱(TCGA)数据库中的相关宫颈腺癌数据集分别进行信号通路和免疫细胞浸润分析,初步揭示RUNX1在宫颈腺癌中的作用机制。结果:免疫组织化学检测结果与患者临床病理资料进行相关性分析显示,RUNX1蛋白在宫颈腺癌中的高表达与患者的总生存期和病理分期呈显著负相关(P<0.05)。对HPA数据库分析发现RUNX1蛋白在宫颈腺癌组织中的表达水平显著高于正常宫颈组织;通过分析 TCGA 数据库中的宫颈腺癌数据集,GSVA 评分分析显示 RUNX1 高表达主要富集的通路有有丝分裂纺锤体、Hedgehog通路、TGF-β通路、Wnt/β-catenin信号通路和p53通路;免疫细胞浸润分析显示,RUNX1表达与中性粒细胞浸润密切相关。结论:RUNX1在宫颈腺癌中高表达,且RUNX1高表达与患者不良预后显著相关,可能成为宫颈腺癌患者预后预测的潜在标志物。

关键词: 宫颈腺癌, RUNX1, 预后, 免疫细胞浸润

Abstract: OBJECTIVE: Cervical adenocarcinoma is markedly distinct from cervical squamous cell carcinoma due to its highly aggressive nature, lower response to radiotherapy, poor prognosis and reduced survival rates. This study aimed to investigate the expression level of RUNX1 in cervical adenocarcinoma tissues and its association with patient prognosis. METHODS: Tumor tissue samples from 37 cervical adenocarcinoma patients were collected. RUNX1 expression in tumor tissues was detected by immunohistochemistry (IHC), and its correlation with clinicopathological parameters and prognosis was statistically analyzed. The Human Protein Atlas (HPA) database was used to analyze the protein expression level of RUNX1 in cervical adenocarcinoma tissues. Gene Set Variation Analysis (GSVA) scoring and the TIMER2.0 platform were utilized to perform signaling pathway enrichment and immune cell infiltration analyses, respectively, using cervical adenocarcinoma datasets from The Cancer Genome Atlas (TCGA) to preliminarily elucidate the mechanistic role of RUNX1 in cervical adenocarcinoma. RESULTS: Immunohistochemistry results demonstrated that RUNX1 expression in cervical adenocarcinoma showed significant differences correlated with patient prognosis and pathological stage (P<0.05). Patients in the RUNX1 high-expression group exhibited shorter overall survival and more advanced pathological stages. Analysis of the HPA database revealed that the protein expression level of RUNX1 was significantly higher than in normal cervical tissues. GSVA of cervical adenocarcinoma datasets from TCGA revealed that RUNX1 high expression was predominantly enriched in pathways including mitotic spindle assembly,Hedgehog signaling,TGF-β signaling,Wnt/β-catenin signaling, and p53 signaling. Immune cell infiltration analysis via TIMER2.0 indicated a significant correlation between RUNX1 expression and neutrophil infiltration. CONCLUSION: RUNX1 was found to be highly expressed in cervical adenocarcinoma and its overexpression was significantly associated with adverse prognosis,suggesting its potential as a prognostic biomarker for cervical adenocarcinoma patients.

Key words: cervical adenocarcinoma, RUNX1, prognosis, immune cell infiltration

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