Evidence map›Paper›PMID 42724522›Full record

ArticleTranslational cancer research2026

PSMB8: an immune-related prognostic marker for low-grade gliomas.

Xinyu Yang, Zhuofan Li, Luyang Xu, Waner Wei, Zewei Tu, Xiaoyan Long, Jia Liu, Jingying Li, Xingen Zhu

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Article in Translational cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Xinyu Yang *Department of Neurology, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China.ORCID https://orcid.org/0000-0003-1847-3263
Zhuofan Li *Jiangxi Province Key Laboratory of Neurological Diseases, Nanchang, China.
Luyang Xu *Department of Emergency Medicine, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Waner Wei *Department of Ultrasound, Honggutan District Maternal and Child Health Hospital, Nanchang, China.
Zewei TuJiangxi Province Key Laboratory of Neurological Diseases, Nanchang, China.
Xiaoyan LongEast China Institute of Digital Medical Engineering, Shangrao, China.
Jia LiuDepartment of Neuroscience, Yale Medicine School, Yale University, New Haven, CT, USA.
Jingying LiDepartment of Comprehensive Intensive Care Unit, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China.
Xingen ZhuJiangxi Province Key Laboratory of Neurological Diseases, Nanchang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Glioma is the most common primary intracranial tumor in adults. As a subunit of immune proteasome, proteasome subunit beta type-8 (PSMB8) may regulate the progression of glioma via participating in degradation and presentation of tumor antigenic peptides, but its prognostic and clinical applicant usage is under investigation. Therefore, this study aimed to comprehensively evaluate the prognostic significance of PSMB8 in low-grade glioma (LGG) and to elucidate its association with the tumor immune microenvironment and potential as a predictor for immunotherapy response. Methods: Transcriptome data were downloaded from The Cancer Genome Atlas (TCGA), Chinese Glioma Genome Atlas (CGGA), Gene Expression Omnibus (GEO) repositories. The correlations between PSMB8 expression and the clinicopathological features of LGG were investigated in our study, and the prognostic role of PSMB8 in LGGs was assessed fully and comprehensively. Furthermore, we evaluated the correlation between PSMB8 expression and LGG immune environment via the experiments and bioinformatic analysis. Results: Our results indicated that, PSMB8 were highly expressed in most tumor tissues, including LGG. Lower expression of PSMB8 was significantly correlated with lower World Health Organization (WHO) grade and isocitrate dehydrogenase (IDH) mutation status. Moreover, PSMB8 showed a promising prognostic ability for LGG patients via nomogram model and receiver operating characteristic (ROC) curves. Association analysis showed that PSMB8 expression was associated with immune cell infiltration in a variety of tumors, including LGG. Our experiments validated the positive correlation between PSMB8 expression and M2-macrophage infiltration level in clinical LGG tissues and invasive ability of LGG cell. Conclusions: PSMB8 could be used as one of the prognostic indicators of LGG and it could regulate the LGG cell migratory and invasive ability. Besides, PSMB8 is expected to be a promising biomarker of cancer immunotherapy.

Indexed as

immune-microenvironmentimmunotherapyLow-grade glioma (LGG)proteasome subunit beta type-8 (PSMB8)

Identifiers

PMID42724522
PMCPMC13559615

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