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首页|期刊导航|广东医学|COL7A1的上调与肺腺癌的预后不良和免疫细胞浸润的生物信息学分析

COL7A1的上调与肺腺癌的预后不良和免疫细胞浸润的生物信息学分析

俞静 张陈霏

广东医学2024,Vol.45Issue(8):1053-1059,7.
广东医学2024,Vol.45Issue(8):1053-1059,7.DOI:10.13820/j.cnki.gdyx.20240983

COL7A1的上调与肺腺癌的预后不良和免疫细胞浸润的生物信息学分析

Bioinformatics analysis of upregulated COL7A1 in lung adenocarcinoma:prognosis and immune cell infiltration

俞静 1张陈霏2

作者信息

  • 1. 南通市第二人民医院检验科(江苏南通 226002)
  • 2. 南通大学附属肿瘤医院肿瘤内科(江苏南通 226361)
  • 折叠

摘要

Abstract

Objective To investigate the expression of COL7A1 in lung adenocarcinoma,its prognostic value,and its relationship with immune cell infiltration in the tumor microenvironment.Methods RNA-Seq data and clinical information from TCGA and GEO databases were analyzed to assess COL7A1 mRNA expression.Protein expression was e-valuated through proteomic analysis.The diagnostic value of COL7A1 in lung adenocarcinoma was assessed using ROC curves.Prognostic value was evaluated using Cox regression and Kaplan-Meier survival analyses,and a clinical predic-tion model was established.The TIME2.0 database was used to evaluate the correlation between COL7A1 and immune cell infiltration.RT-qPCR was performed to validate COL7 A1 expression.Results COL7A1 was significantly upregulated in lung adenocarcinoma tissues,particularly in those with distant metastasis and at advanced stages.COL7A1 showed diag-nostic and prognostic value in lung adenocarcinoma,with high COL7A1 expression being an independent risk factor.The constructed prediction model was more accurate than TNM staging.Additionally,COL7A1 was positively correlated with tumor fibroblast infiltration and negatively correlated with neutrophil infiltration.Conclusion High expression of COL7A1 in lung adenocarcinoma indicates poor prognosis and suggests that COL7A1 could be a potential target for immunotherapy.

关键词

肺腺癌/COL7A1/预后/免疫细胞/生物信息学

Key words

lung adenocarcinoma/COL7A1/prognosis/immune cells/bioinformatics

分类

医药卫生

引用本文复制引用

俞静,张陈霏..COL7A1的上调与肺腺癌的预后不良和免疫细胞浸润的生物信息学分析[J].广东医学,2024,45(8):1053-1059,7.

基金项目

南通市卫生健康委员会指令性青年课题(QN2022038) (QN2022038)

广东医学

OACSTPCD

1001-9448

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