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Autori principali: Yang, Xiaoping, Liu, Yongji, Jiang, Wen, Liu, Xiaochun, Zhang, Xiaonan, Liu, Huiying, Xing, Daijun, Wang, Keer, Zheng, Xin, Jiang, Wenqing
Natura: Artículo científico
Lingua:en
Pubblicazione: Scientific reports 2025
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Accesso online:https://pubmed.ncbi.nlm.nih.gov/40851084/
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author Yang, Xiaoping
Liu, Yongji
Jiang, Wen
Liu, Xiaochun
Zhang, Xiaonan
Liu, Huiying
Xing, Daijun
Wang, Keer
Zheng, Xin
Jiang, Wenqing
author_facet Yang, Xiaoping
Liu, Yongji
Jiang, Wen
Liu, Xiaochun
Zhang, Xiaonan
Liu, Huiying
Xing, Daijun
Wang, Keer
Zheng, Xin
Jiang, Wenqing
Yang, Xiaoping
Liu, Yongji
Jiang, Wen
Liu, Xiaochun
Zhang, Xiaonan
Liu, Huiying
Xing, Daijun
Wang, Keer
Zheng, Xin
Jiang, Wenqing
collection PubMed - marine biology
contents Identification of SUMOylation modifiers involved in lung adenocarcinoma progression and Osimertinib resistance by integrated bioinformatics analysis. Yang, Xiaoping Liu, Yongji Jiang, Wen Liu, Xiaochun Zhang, Xiaonan Liu, Huiying Xing, Daijun Wang, Keer Zheng, Xin Jiang, Wenqing Humans Adenocarcinoma of Lung Drug Resistance, Neoplasm Lung Neoplasms Sumoylation Acrylamides Computational Biology Disease Progression Aniline Compounds Gene Expression Regulation, Neoplastic Prognosis Biomarkers, Tumor Signal Transduction Gene Expression Profiling Indoles Pyrimidines This study investigates the mechanisms of Osimertinib resistance in lung adenocarcinoma (LUAD) by identifying prognostic genes associated with SUMOylation. We performed differential expression analysis to identify differentially expressed genes (DEGs) in LUAD samples, Osimertinib-tolerant cell samples and SUMOylation-related genes (SRGs). Utilizing Cox regression and LASSO regression, we developed a prognostic model that highlighted five key prognostic genes-BIRC5, AURKA, BLM, NR3C2, and NDC1. These genes were significantly associated with LUAD progression, revealing their predominant expression in epithelial cells, which play a vital role in tumor development. Furthermore, we explored the biological functions and signaling pathways linked to these prognostic genes, discovering that their expression levels and corresponding risk scores could serve as indicators of CD4 T cell and memory B cell activation. The enriched signaling pathways in LUAD were regulated by ubiquitin-related small modifiers, highlighting the complex interplay between SUMOylation and tumor biology. Our findings suggest the important role of SUMOylation-regulated genes in LUAD progression and Osimertinib resistance, suggesting their potential as valuable biomarkers for prognosis and therapeutic targets to enhance treatment strategies for patients with EGFR-mutant lung adenocarcinoma.
format Artículo científico
id pubmed_40851084
institution PubMed
language en
publishDate 2025
publisher Scientific reports
record_format pubmed
spellingShingle Identification of SUMOylation modifiers involved in lung adenocarcinoma progression and Osimertinib resistance by integrated bioinformatics analysis.
Yang, Xiaoping
Liu, Yongji
Jiang, Wen
Liu, Xiaochun
Zhang, Xiaonan
Liu, Huiying
Xing, Daijun
Wang, Keer
Zheng, Xin
Jiang, Wenqing
Humans
Adenocarcinoma of Lung
Drug Resistance, Neoplasm
Lung Neoplasms
Sumoylation
Acrylamides
Computational Biology
Disease Progression
Aniline Compounds
Gene Expression Regulation, Neoplastic
Prognosis
Biomarkers, Tumor
Signal Transduction
Gene Expression Profiling
Indoles
Pyrimidines
Identification of SUMOylation modifiers involved in lung adenocarcinoma progression and Osimertinib resistance by integrated bioinformatics analysis. Yang, Xiaoping Liu, Yongji Jiang, Wen Liu, Xiaochun Zhang, Xiaonan Liu, Huiying Xing, Daijun Wang, Keer Zheng, Xin Jiang, Wenqing Humans Adenocarcinoma of Lung Drug Resistance, Neoplasm Lung Neoplasms Sumoylation Acrylamides Computational Biology Disease Progression Aniline Compounds Gene Expression Regulation, Neoplastic Prognosis Biomarkers, Tumor Signal Transduction Gene Expression Profiling Indoles Pyrimidines This study investigates the mechanisms of Osimertinib resistance in lung adenocarcinoma (LUAD) by identifying prognostic genes associated with SUMOylation. We performed differential expression analysis to identify differentially expressed genes (DEGs) in LUAD samples, Osimertinib-tolerant cell samples and SUMOylation-related genes (SRGs). Utilizing Cox regression and LASSO regression, we developed a prognostic model that highlighted five key prognostic genes-BIRC5, AURKA, BLM, NR3C2, and NDC1. These genes were significantly associated with LUAD progression, revealing their predominant expression in epithelial cells, which play a vital role in tumor development. Furthermore, we explored the biological functions and signaling pathways linked to these prognostic genes, discovering that their expression levels and corresponding risk scores could serve as indicators of CD4 T cell and memory B cell activation. The enriched signaling pathways in LUAD were regulated by ubiquitin-related small modifiers, highlighting the complex interplay between SUMOylation and tumor biology. Our findings suggest the important role of SUMOylation-regulated genes in LUAD progression and Osimertinib resistance, suggesting their potential as valuable biomarkers for prognosis and therapeutic targets to enhance treatment strategies for patients with EGFR-mutant lung adenocarcinoma.
title Identification of SUMOylation modifiers involved in lung adenocarcinoma progression and Osimertinib resistance by integrated bioinformatics analysis.
topic Humans
Adenocarcinoma of Lung
Drug Resistance, Neoplasm
Lung Neoplasms
Sumoylation
Acrylamides
Computational Biology
Disease Progression
Aniline Compounds
Gene Expression Regulation, Neoplastic
Prognosis
Biomarkers, Tumor
Signal Transduction
Gene Expression Profiling
Indoles
Pyrimidines
url https://pubmed.ncbi.nlm.nih.gov/40851084/