Biomedicine & Pharmacotherapy, Journal Year: 2024, Volume and Issue: 182, P. 117769 - 117769
Published: Dec. 16, 2024
Language: Английский
Biomedicine & Pharmacotherapy, Journal Year: 2024, Volume and Issue: 182, P. 117769 - 117769
Published: Dec. 16, 2024
Language: Английский
Scientific Reports, Journal Year: 2025, Volume and Issue: 15(1)
Published: Feb. 17, 2025
Language: Английский
Citations
0Cell Communication and Signaling, Journal Year: 2025, Volume and Issue: 23(1)
Published: April 5, 2025
Abstract Background Lysyl oxidases (LOX/LOXL1-4) are crucial for cancer progression, yet their transcriptional regulation, potential therapeutic targeting, prognostic value and involvement in immune regulation remain poorly understood. This study comprehensively evaluates LOX/LOXL expression highlights types where targeting these enzymes developing LOX/LOXL-based models could have significant clinical relevance. Methods We assessed the association of with survival drug sensitivity via analyzing public datasets (including bulk single-cell RNA sequencing data six from Gene Expression Omnibus (GEO), Chinese Glioma Genome Atlas (CGGA) Cancer Program (TCGA)). performed comprehensive machine learning-based bioinformatics analyses, including unsupervised consensus clustering, a total 10 machine-learning algorithms prediction Connectivity map tool prediction. Results The significance family was evaluated across 33 types. Overexpression showed strong correlation tumor progression poor survival, particularly glioma. Therefore, we developed novel model glioma by integrating its co-expressed genes. highly predictive overall patients, indicating utility assessment. Furthermore, our analysis uncovered distinct LOXL2-overexpressing malignant cell population recurrent glioma, characterized activation collagen, laminin, semaphorin-3 pathways, along enhanced epithelial-mesenchymal transition. Apart revealed role LOXL3 overexpression macrophages predicting response to checkpoint blockade bladder renal cancers. Given pro-tumor genes most analyzed cancers, identified compounds, such as VEGFR inhibitor cediranib, target pan-LOX/LOXL cancer. Conclusions Our provides insights into pathogenesis treatment,
Language: Английский
Citations
0Biomedicine & Pharmacotherapy, Journal Year: 2024, Volume and Issue: 182, P. 117769 - 117769
Published: Dec. 16, 2024
Language: Английский
Citations
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