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pmid:40634444

Anoikis-related biomarkers PARP1 and SDCBP as diagnostic and therapeutic targets for asthma.

Li-Jie Yang · Na-Na Song · Ni-Shan Deng · Miao-Juan Zhu · Qing-Qing Li · Si-Si Huang · Xiu Shi · Zhen-Hong Hu · Han-Xiang Nie

Scientific reports · 2025 doi:10.1038/s41598-025-09979-9

Paper

complete

Experiment

partial

Data

partial

Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
Anoikis-related biomarkers PARP1 and SDCBP as diagnostic and therapeutic targets for asthma.
doi
10.1038/s41598-025-09979-9
pmid
40634444
authors array · 9 items
[0]
Li-Jie Yang
[1]
Na-Na Song
[2]
Ni-Shan Deng
[3]
Miao-Juan Zhu
[4]
Qing-Qing Li
[5]
Si-Si Huang
[6]
Xiu Shi
[7]
Zhen-Hong Hu
[8]
Han-Xiang Nie
journal
Scientific reports
year
2025
abstract
This study aims to explore the association between anoikis-related genes (ARGs) and asthma. The dataset GSE143303 for asthma were sourced from the GEO database, while ARGs were retrieved from the Harmonizome web portal and the GeneCards database. Differentially expressed genes (DEGs) identification and GO, KEGG enrichment analysis were performed to reveal potential biological pathways. To identify hub anoikis-related DEGs (hub ARDEGs), we employed WGCNA and machine learning methods including LASSO and Random Forest. Additionally, we constructed risk prediction nomogram model and ROC curves to evaluate the asthma diagnostic value of hub ARDEGs. SsGSEA immune infiltration analysis was used to analyze the role of hub ARDEGs in the asthma immune microenvironment. Finally, miRNAs and transcription factors (TFs) interacting with these hub ARDEGs were investigated. DEGs of ARGs between asthma and healthy controls, along with WGCNA, led to the identification of six ARDEGs. GO and KEGG analyses revealed that these ARDEGs were primarily involved in the apoptotic signaling pathway and adherens junctions. Machine learning methods further narrowed down the six ARDEGs to two hub ARDEGs: PARP1 and SDCBP, which were significantly upregulated in asthma and validated using the GSE147878 and experimental models. Based on these two hub ARDEGs, a risk prediction model for asthma was developed, demonstrating strong diagnostic potential and tissue specificity in endobronchial biopsies. Immune analysis revealed variations in immune cell infiltration within asthma samples correlated with hub ARDEGs. Additionally, the miRNA-TF-mRNA interaction network of hub ARDEGs highlights the complexity of the regulatory process. The process of anoikis, immune dysregulation, and asthma are closely interconnected. The anoikis-related biomarkers PARP1 and SDCBP may serve as diagnostic markers and therapeutic targets for asthma.
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Hub ARDEGs were identified using the least absolute shrinkage and selection operator (LASSO) regression and Random Forest (RF) methods.
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The data supporting the findings of this study are publicly available in the Gene Expression Omnibus at https://www.ncbi.nlm.nih.gov/geo/, with reference numbers GSE143303, GSE147878, GSE64913, GSE137268, and GSE27876; the Harmonizome at https://maayanlab.cloud/Harmonizome/; and the GeneCards database at https://www.genecards.org/. Further inquiries can be directed to the corresponding authors.
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The data supporting the findings of this study are publicly available in the Gene Expression Omnibus at https://www.ncbi.nlm.nih.gov/geo/, with reference numbers GSE143303, GSE147878, GSE64913, GSE137268, and GSE27876; the Harmonizome at https://maayanlab.cloud/Harmonizome/; and the GeneCards database at https://www.genecards.org/. Further inquiries can be directed to the corresponding authors.
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DEGs of ARGs between asthma and healthy controls, along with WGCNA, led to the identification of six ARDEGs.
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DEGs of ARGs between asthma and healthy controls, along with WGCNA, led to the identification of six ARDEGs.
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DEGs of ARGs between asthma and healthy controls, along with WGCNA, led to the identification of six ARDEGs.
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Altered epithelial gene expression in peripheral airways of severe asthma
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Hub ARDEGs were identified using the least absolute shrinkage and selection operator (LASSO) regression and Random Forest (RF) methods.
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The data supporting the findings of this study are publicly available in the Gene Expression Omnibus at https://www.ncbi.nlm.nih.gov/geo/, with reference numbers GSE143303, GSE147878, GSE64913, GSE137268, and GSE27876; the Harmonizome at https://maayanlab.cloud/Harmonizome/; and the GeneCards database at https://www.genecards.org/. Further inquiries can be directed to the corresponding authors.
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The dataset GSE143303 for asthma were sourced from the GEO database, while ARGs were retrieved from the Harmonizome web portal and the GeneCards database. Differentially expressed genes (DEGs) identification and GO, KEGG enrichment analysis were performed to reveal potential biological pathways. To identify hub anoikis-related DEGs (hub ARDEGs), we employed WGCNA and machine learning methods including LASSO and Random Forest. Additionally, we constructed risk prediction nomogram model and ROC curves to evaluate the asthma diagnostic value of hub ARDEGs. SsGSEA immune infiltration analysis was used to analyze the role of hub ARDEGs in the asthma immune microenvironment. Finally, miRNAs and transcription factors (TFs) interacting with these hub ARDEGs were investigated. DEGs of ARGs between asthma and healthy controls, along with WGCNA, led to the identification of six ARDEGs. GO and KEGG analyses revealed that these ARDEGs were primarily involved in the apoptotic signaling pathway and adherens junctions. Machine learning methods further narrowed down the six ARDEGs to two hub ARDEGs: PARP1 and SDCBP, which were significantly upregulated in asthma and validated using the GSE147878 and experimental models. Based on these two hub ARDEGs, a risk prediction model for asthma was developed, demonstrating strong diagnostic potential and tissue specificity in endobronchial biopsies. Immune analysis revealed variations in immune cell infiltration within asthma samples correlated with hub ARDEGs. Additionally, the miRNA-TF-mRNA interaction network of hub ARDEGs highlights the complexity of the regulatory process. The process of anoikis, immune dysregulation, and asthma are closely interconnected. 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