Characterization of NOD-like receptor-based molecular heterogeneity in glioma and its association with immune micro-environment and metabolism reprogramming

Background and purposeThe characteristics and role of NOD-like receptor (NLR) signaling pathway in high-grade gliomas were still unclear. This study aimed to reveal the association of NLR with clinical heterogeneity of glioblastoma (GBM) patients, and to explore the role of NLR pathway hub genes in...

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Main Authors: Chunlin Lu, Huihao Ma, Jie Wang, Fei Sun, Mingyang Fei, Ying Li, Jing Liu, Bin Dong
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Immunology
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Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2024.1498583/full
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author Chunlin Lu
Huihao Ma
Jie Wang
Fei Sun
Fei Sun
Mingyang Fei
Ying Li
Jing Liu
Bin Dong
author_facet Chunlin Lu
Huihao Ma
Jie Wang
Fei Sun
Fei Sun
Mingyang Fei
Ying Li
Jing Liu
Bin Dong
author_sort Chunlin Lu
collection DOAJ
description Background and purposeThe characteristics and role of NOD-like receptor (NLR) signaling pathway in high-grade gliomas were still unclear. This study aimed to reveal the association of NLR with clinical heterogeneity of glioblastoma (GBM) patients, and to explore the role of NLR pathway hub genes in the occurrence and development of GBM.MethodsTranscriptomic data from 496 GBM patients with complete prognostic information were obtained from the TCGA, GEO, and CGGA databases. Using the NMF clustering algorithm and the expression profiles of NLR genes, these 496 GBM patients were classified into different clinical subtypes. The pathway activity of NLR and the immune micro-environment characteristics were then compared between these subtypes. A novel and accurate NLR expression profile-based prognostic marker for GBM was developed using LASSO and COX regression analysis.ResultsBased on the NLR gene expression profile, GBM patients were accurately divided into two clinical subtypes (C1 and C2) with different clinical outcomes. The two groups of patients showed different immune microenvironment characteristics and metabolic characteristics, which might be the potential reason for the difference in prognosis. Differential expression and enrichment analyzes revealed intrinsic gene signature differences between C1 and C2 subtypes. Based on the differential expression profiles of C1 and C2, prognostic molecular markers related to NLR were developed. The AUC value of the 3-year ROC curve ranged from 0.601 to 0.846, suggesting its potential clinical significance. Single-cell sequencing analysis showed that the NLR gene was mainly active in myeloid cells within GBM. The random forest algorithm identified the crucial role of TRIP6 gene in NLR pathway. Molecular biology experiments confirmed that TRIP6 was abnormally overexpressed in GBM. Knockdown of TRIP6 gene can significantly inhibit the proliferation and migration ability of GBM cells.ConclusionThe NLR signaling pathway plays a critical role in regulating immune microenvironment and metabolism reprogramming of GBM. TRIP6 is a potential hub gene within the NLR pathway and affects the malignant biological behavior of GBM cells.
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spelling doaj-art-81adc3e93b7a4673b987ebbc922edee92025-01-15T05:11:09ZengFrontiers Media S.A.Frontiers in Immunology1664-32242025-01-011510.3389/fimmu.2024.14985831498583Characterization of NOD-like receptor-based molecular heterogeneity in glioma and its association with immune micro-environment and metabolism reprogrammingChunlin Lu0Huihao Ma1Jie Wang2Fei Sun3Fei Sun4Mingyang Fei5Ying Li6Jing Liu7Bin Dong8Department of Neurosurgery, First Affiliated Hospital of Dalian Medical University, Dalian, ChinaDepartment of Neurosurgery, First Affiliated Hospital of Dalian Medical University, Dalian, ChinaDepartment of Stem Cell and Clinical Research, First Affiliated Hospital of Dalian Medical University, Dalian, ChinaDepartment of Neurosurgery, First Affiliated Hospital of Dalian Medical University, Dalian, ChinaDepartment of Neurosurgery, Xinhua Hospital Affiliated to Dalian University, Dalian, ChinaDepartment of Neurosurgery, First Affiliated Hospital of Dalian Medical University, Dalian, ChinaDepartment of Stem Cell and Clinical Research, First Affiliated Hospital of Dalian Medical University, Dalian, ChinaThe Administration center, First Affiliated Hospital of Dalian Medical University, Dalian, ChinaDepartment of Neurosurgery, First Affiliated Hospital of Dalian Medical University, Dalian, ChinaBackground and purposeThe characteristics and role of NOD-like receptor (NLR) signaling pathway in high-grade gliomas were still unclear. This study aimed to reveal the association of NLR with clinical heterogeneity of glioblastoma (GBM) patients, and to explore the role of NLR pathway hub genes in the occurrence and development of GBM.MethodsTranscriptomic data from 496 GBM patients with complete prognostic information were obtained from the TCGA, GEO, and CGGA databases. Using the NMF clustering algorithm and the expression profiles of NLR genes, these 496 GBM patients were classified into different clinical subtypes. The pathway activity of NLR and the immune micro-environment characteristics were then compared between these subtypes. A novel and accurate NLR expression profile-based prognostic marker for GBM was developed using LASSO and COX regression analysis.ResultsBased on the NLR gene expression profile, GBM patients were accurately divided into two clinical subtypes (C1 and C2) with different clinical outcomes. The two groups of patients showed different immune microenvironment characteristics and metabolic characteristics, which might be the potential reason for the difference in prognosis. Differential expression and enrichment analyzes revealed intrinsic gene signature differences between C1 and C2 subtypes. Based on the differential expression profiles of C1 and C2, prognostic molecular markers related to NLR were developed. The AUC value of the 3-year ROC curve ranged from 0.601 to 0.846, suggesting its potential clinical significance. Single-cell sequencing analysis showed that the NLR gene was mainly active in myeloid cells within GBM. The random forest algorithm identified the crucial role of TRIP6 gene in NLR pathway. Molecular biology experiments confirmed that TRIP6 was abnormally overexpressed in GBM. Knockdown of TRIP6 gene can significantly inhibit the proliferation and migration ability of GBM cells.ConclusionThe NLR signaling pathway plays a critical role in regulating immune microenvironment and metabolism reprogramming of GBM. TRIP6 is a potential hub gene within the NLR pathway and affects the malignant biological behavior of GBM cells.https://www.frontiersin.org/articles/10.3389/fimmu.2024.1498583/fullNLR pathwayGBMimmune microenvironmentmetabolism reprogrammingclinical heterogeneityTRIP6
spellingShingle Chunlin Lu
Huihao Ma
Jie Wang
Fei Sun
Fei Sun
Mingyang Fei
Ying Li
Jing Liu
Bin Dong
Characterization of NOD-like receptor-based molecular heterogeneity in glioma and its association with immune micro-environment and metabolism reprogramming
Frontiers in Immunology
NLR pathway
GBM
immune microenvironment
metabolism reprogramming
clinical heterogeneity
TRIP6
title Characterization of NOD-like receptor-based molecular heterogeneity in glioma and its association with immune micro-environment and metabolism reprogramming
title_full Characterization of NOD-like receptor-based molecular heterogeneity in glioma and its association with immune micro-environment and metabolism reprogramming
title_fullStr Characterization of NOD-like receptor-based molecular heterogeneity in glioma and its association with immune micro-environment and metabolism reprogramming
title_full_unstemmed Characterization of NOD-like receptor-based molecular heterogeneity in glioma and its association with immune micro-environment and metabolism reprogramming
title_short Characterization of NOD-like receptor-based molecular heterogeneity in glioma and its association with immune micro-environment and metabolism reprogramming
title_sort characterization of nod like receptor based molecular heterogeneity in glioma and its association with immune micro environment and metabolism reprogramming
topic NLR pathway
GBM
immune microenvironment
metabolism reprogramming
clinical heterogeneity
TRIP6
url https://www.frontiersin.org/articles/10.3389/fimmu.2024.1498583/full
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