| Literature DB >> 33613515 |
Min Chao1, Nan Liu2, Zhichuan Sun1, Yongli Jiang3, Tongtong Jiang4, Meng Xv1, Lintao Jia4, Yanyang Tu2, Liang Wang1.
Abstract
Gliomas are brain and spinal cord malignancies characterized by high malignancy, high recurrence and poor prognosis, the underlying mechanisms of which remain largely elusive. Here, we found that the Sry-related high mobility group box (Sox) family transcription factor, Sox9, was upregulated and correlated with poor prognosis of clinical gliomas. Sox9 promotes migration and invasion of glioma cells and in vivo development of xenograft tumors from inoculated glioma cells. Sox9 functions downstream of the transforming growth factor-β (TGF-β) pathway, in which TGF-β signaling prevent proteasomal degradation of the Sox9 protein in glioma cells. These findings provide novel insight into the wide interplay between TGF-β signaling and oncogenic transcription factors, and have implications for targeted therapy and prognostic assessment of gliomas.Entities:
Keywords: Sox9; glioma; invasion; migration; transforming growth factor-β
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Year: 2021 PMID: 33613515 PMCID: PMC7886799 DOI: 10.3389/fimmu.2020.592080
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561