To explore the potential of LOXL2 as a biomarker in glioma and construct a genomic integrated clinical prognostic model

BackgroundGlioma is a common invasive tumor of the central nervous system, and its pathological features significantly impair the quality of life of patients, with high mortality risk and easy recurrence. For glioma Lysine Oxidase 2(LOXL2), there are few reports in the scholarly literature. Based on...

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Main Authors: Hongjuan Wang, Qunli Li, Xiangtao Zheng, Weibiao Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-07-01
Series:Frontiers in Oncology
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Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2025.1602475/full
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author Hongjuan Wang
Qunli Li
Xiangtao Zheng
Weibiao Chen
author_facet Hongjuan Wang
Qunli Li
Xiangtao Zheng
Weibiao Chen
author_sort Hongjuan Wang
collection DOAJ
description BackgroundGlioma is a common invasive tumor of the central nervous system, and its pathological features significantly impair the quality of life of patients, with high mortality risk and easy recurrence. For glioma Lysine Oxidase 2(LOXL2), there are few reports in the scholarly literature. Based on the current situation of the insufficiency of current therapies, this study focuses on analyzing the biological function of LOXL2 in the occurrence and development of glioma by bioinformatics technology, and systematically evaluates the potential association between this molecular marker and the prognosis of patients. Through the integration of clinical data and molecular mechanism research, this study aims to provide a new theoretical basis for improving the diagnosis and treatment strategy of glioma.MethodsIntegrated CCGA (exploratory) and TCGA (validation) cohorts. Analyzed LOXL2 expression patterns, GO/KEGG pathways, immune infiltration, single-cell distribution (scRNA-seq), and survival associations. Prognostic models were established via KM survival, COX regression, nomogram, and DCA.ResultsLOXL2 overexpression correlated with higher glioma malignancy (P<0.001), particularly in IDH wild-type and 1p/19q non-codeleted subtypes (P<0.001). GO/KEGG revealed LOXL2 involvement in ECM remodeling. Immune analysis showed LOXL2 mediates macrophage-neutrophil immunosuppressive networks. scRNA-seq localized LOXL2 in tumor cells, stroma, and macrophages. High LOXL2 predicted worse overall survival (P<0.001). ROC-AUC for 1/3/5-year survival: CCGA: 0.817/0.897/0.925; TCGA: 0.793/0.776/0.730. Respectively, which proved that LOXL2 could be used as an independent prognostic indicator for glioma. Through the construction of nomogram and DCA model evaluation, the results indicate that LOXL2 has important translational value in the prognosis prediction of glioma.ConclusionsThis study revealed that LOXL2 can be used as a potential biomarker in glioma and is correlated with clinical prognosis. LOXL2 may affect the dynamic balance of the tumor microenvironment by regulating the immune function of macrophages and neutrophils in the extracellular matrix (ECM). The prediction model was established based on CCGA clinical data and COX regression analysis of LOXL2 gene expression data, which provides a theoretical foundation for the development of LOXL2-targeted therapy and the construction of genomic integrated prognostic model.
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spelling doaj-art-f89889363f2f4e7c907326740cecd6302025-08-20T02:39:41ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2025-07-011510.3389/fonc.2025.16024751602475To explore the potential of LOXL2 as a biomarker in glioma and construct a genomic integrated clinical prognostic modelHongjuan Wang0Qunli Li1Xiangtao Zheng2Weibiao Chen3Cranial Ultrasound Chamber, Jinhua Traditional Chinese Medicine Hospital, Jinhua, Zhejiang, ChinaSurgical Center, The Second Affiliated Hospital of Wenzhou Medical University, Yuying Children's Hospital, Wenzhou, Zhejiang, ChinaSurgical Center, The Second Affiliated Hospital of Wenzhou Medical University, Yuying Children's Hospital, Wenzhou, Zhejiang, ChinaSurgical Center, The Second Affiliated Hospital of Wenzhou Medical University, Yuying Children's Hospital, Wenzhou, Zhejiang, ChinaBackgroundGlioma is a common invasive tumor of the central nervous system, and its pathological features significantly impair the quality of life of patients, with high mortality risk and easy recurrence. For glioma Lysine Oxidase 2(LOXL2), there are few reports in the scholarly literature. Based on the current situation of the insufficiency of current therapies, this study focuses on analyzing the biological function of LOXL2 in the occurrence and development of glioma by bioinformatics technology, and systematically evaluates the potential association between this molecular marker and the prognosis of patients. Through the integration of clinical data and molecular mechanism research, this study aims to provide a new theoretical basis for improving the diagnosis and treatment strategy of glioma.MethodsIntegrated CCGA (exploratory) and TCGA (validation) cohorts. Analyzed LOXL2 expression patterns, GO/KEGG pathways, immune infiltration, single-cell distribution (scRNA-seq), and survival associations. Prognostic models were established via KM survival, COX regression, nomogram, and DCA.ResultsLOXL2 overexpression correlated with higher glioma malignancy (P<0.001), particularly in IDH wild-type and 1p/19q non-codeleted subtypes (P<0.001). GO/KEGG revealed LOXL2 involvement in ECM remodeling. Immune analysis showed LOXL2 mediates macrophage-neutrophil immunosuppressive networks. scRNA-seq localized LOXL2 in tumor cells, stroma, and macrophages. High LOXL2 predicted worse overall survival (P<0.001). ROC-AUC for 1/3/5-year survival: CCGA: 0.817/0.897/0.925; TCGA: 0.793/0.776/0.730. Respectively, which proved that LOXL2 could be used as an independent prognostic indicator for glioma. Through the construction of nomogram and DCA model evaluation, the results indicate that LOXL2 has important translational value in the prognosis prediction of glioma.ConclusionsThis study revealed that LOXL2 can be used as a potential biomarker in glioma and is correlated with clinical prognosis. LOXL2 may affect the dynamic balance of the tumor microenvironment by regulating the immune function of macrophages and neutrophils in the extracellular matrix (ECM). The prediction model was established based on CCGA clinical data and COX regression analysis of LOXL2 gene expression data, which provides a theoretical foundation for the development of LOXL2-targeted therapy and the construction of genomic integrated prognostic model.https://www.frontiersin.org/articles/10.3389/fonc.2025.1602475/fullLOXL2gliomaclinical prognosisimmune infiltrationprognostic models
spellingShingle Hongjuan Wang
Qunli Li
Xiangtao Zheng
Weibiao Chen
To explore the potential of LOXL2 as a biomarker in glioma and construct a genomic integrated clinical prognostic model
Frontiers in Oncology
LOXL2
glioma
clinical prognosis
immune infiltration
prognostic models
title To explore the potential of LOXL2 as a biomarker in glioma and construct a genomic integrated clinical prognostic model
title_full To explore the potential of LOXL2 as a biomarker in glioma and construct a genomic integrated clinical prognostic model
title_fullStr To explore the potential of LOXL2 as a biomarker in glioma and construct a genomic integrated clinical prognostic model
title_full_unstemmed To explore the potential of LOXL2 as a biomarker in glioma and construct a genomic integrated clinical prognostic model
title_short To explore the potential of LOXL2 as a biomarker in glioma and construct a genomic integrated clinical prognostic model
title_sort to explore the potential of loxl2 as a biomarker in glioma and construct a genomic integrated clinical prognostic model
topic LOXL2
glioma
clinical prognosis
immune infiltration
prognostic models
url https://www.frontiersin.org/articles/10.3389/fonc.2025.1602475/full
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