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<p>Glioblastoma (GBM), the most common and aggressive primary brain tumour, is associated with poor prognosis, primarily due to its stem-like subpopulation, glioblastoma stem cells (GSCs). The deubiquitinase (DUB) family has attracted an increasing amount of attention due to its roles in GSC biology and tumour aggressiveness. In this study, we focused on ubiquitin-specific peptidase 18 (<i>USP18</i>), a member of the DUB family whose role in GBM is poorly understood. Through integrated bioinformatics analyses and experimental investigations using patient-derived samples, cell models, and animal models, we elucidated the role of <i>USP18</i> in enhancing GSC stemness and promoting malignant behaviours. Our findings revealed that <i>USP18</i> expression is significantly elevated in GBM and is correlated with a poor prognosis. Mechanistically, USP18 interacts with SRY-box transcription factor 9 (SOX9), stabilising its protein levels by cleaving K48-linked polyubiquitin chains. Additionally, we identified <i>YY1</i> as a transcriptional regulator of <i>USP18</i>, increasing its expression in GBM cells. These findings reveal that <i>USP18</i> is a potential therapeutic target and highlight the novel <i>YY1/USP18/SOX9</i> signalling axis implicated in GBM progression.</p>

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USP18 deubiquitinates and stabilizes SOX9 to promote the stemness and malignant progression of glioblastoma

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年5月15日

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  • Zhiyuan Liu,
  • Kuo Yu,
  • Kaile Chen,
  • Yi Zhang,
  • Kexiang Dai,
  • Liang Zhao,
  • Peng Zhao

摘要

Glioblastoma (GBM), the most common and aggressive primary brain tumour, is associated with poor prognosis, primarily due to its stem-like subpopulation, glioblastoma stem cells (GSCs). The deubiquitinase (DUB) family has attracted an increasing amount of attention due to its roles in GSC biology and tumour aggressiveness. In this study, we focused on ubiquitin-specific peptidase 18 (USP18), a member of the DUB family whose role in GBM is poorly understood. Through integrated bioinformatics analyses and experimental investigations using patient-derived samples, cell models, and animal models, we elucidated the role of USP18 in enhancing GSC stemness and promoting malignant behaviours. Our findings revealed that USP18 expression is significantly elevated in GBM and is correlated with a poor prognosis. Mechanistically, USP18 interacts with SRY-box transcription factor 9 (SOX9), stabilising its protein levels by cleaving K48-linked polyubiquitin chains. Additionally, we identified YY1 as a transcriptional regulator of USP18, increasing its expression in GBM cells. These findings reveal that USP18 is a potential therapeutic target and highlight the novel YY1/USP18/SOX9 signalling axis implicated in GBM progression.