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Front Oncol. 2021 Aug 20;11:701933. doi: 10.3389/fonc.2021.701933. eCollection 2021.

Caveolin-1, a Key Mediator Across Multiple Pathways in Glioblastoma and an Independent Negative Biomarker of Patient Survival.

Frontiers in oncology

Chiara Moriconi, Prospero Civita, Catia Neto, Geoffrey J Pilkington, Mark Gumbleton

Affiliations

  1. School of Pharmacy and Pharmaceutical Sciences, College of Biomedical and Life Sciences, Cardiff University, Cardiff, United Kingdom.
  2. Department of Pathology and Cell Biology, Columbia University, New York Presbyterian Hospital, New York, NY, United States.
  3. Brain Tumour Research Centre, School of Pharmacy & Biomedical Sciences, University of Portsmouth, Portsmouth, United Kingdom.
  4. Department of Basic and Clinical Neuroscience, Division of Neuroscience, Institute of Psychiatry & Neurology, King's College London, London, United Kingdom.

PMID: 34490102 PMCID: PMC8417742 DOI: 10.3389/fonc.2021.701933

Abstract

Glioblastoma (GB) remains an aggressive malignancy with an extremely poor prognosis. Discovering new candidate drug targets for GB remains an unmet medical need. Caveolin-1 (Cav-1) has been shown to act variously as both a tumour suppressor and tumour promoter in many cancers. The implications of Cav-1 expression in GB remains poorly understood. Using clinical and genomic databases we examined the relationship between tumour Cav-1 gene expression (including its spatial distribution) and clinical pathological parameters of the GB tumour and survival probability in a TCGA cohort (n=155) and CGGA cohort (n=220) of GB patients. High expression of Cav-1 represented a significant independent predictor of shortened survival (HR = 2.985, 5.1

Copyright © 2021 Moriconi, Civita, Neto, Pilkington and Gumbleton.

Keywords: CGGA; TCGA; caveolin-1; gender; glioblastoma; invasion; prognostic; survival

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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