Identification and validation of potential prognostic biomarkers in glioblastoma via the mesenchymal stem cell infiltration level

被引:0
|
作者
Wang, Shengyu [1 ]
Mao, Senlin [1 ]
Li, Xiaofu [2 ]
Yang, Dan [1 ]
Zhou, Yinglian [1 ]
Yue, Hui [1 ]
Li, Bing [1 ]
Li, Wei [3 ]
Li, Chengyun [1 ]
Zhang, Xuemei [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 2, Dept Neurol, Harbin, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 2, Dept Magnet Resonance Imaging, Harbin, Peoples R China
[3] Heilongjiang Hosp, Dept Neurol, Harbin, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2024年 / 14卷
关键词
glioblastoma; mesenchymal stem cell; tumor microenvironment; immune checkpoint; prognostic model; MATRIX;
D O I
10.3389/fonc.2024.1406186
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims Mesenchymal stem cells (MSCs) are key components in promoting glioblastoma (GBM) progression. This study aimed to explore new therapeutic targets and related pathogenic mechanisms based on different MSCs infiltration levels in GBM patients.Methods We estimated the relationship between cell infiltration and prognosis of GBM. Subsequently, key risk genes were identified and prognostic models were constructed by LASSO-Cox analysis. The risk genes were validated by five independent external cohorts, single-cell RNA analysis, and immunohistochemistry of human GBM tissues. TIDE analysis predicted responsiveness to immune checkpoint inhibitors in different risk groups.Results The MSCs infiltration level was negatively associated with survival in GBM patients. LOXL1, LOXL4, and GUCA1A are key risk genes that promote GBM progression and may act through complex intercellular communication.Conclusion This research has provided a comprehensive study for exploring the MSCs infiltration environment on GBM progression, which could shed light on novel biomarkers and mechanisms involved in GBM progression.
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页数:12
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