4.7 Article

Fibulin-2: A Novel Biomarker for Differentiating Grade II from Grade I Meningiomas

Journal

Publisher

MDPI
DOI: 10.3390/ijms22020560

Keywords

meningioma; atypical; benign; biomarker; plasma

Funding

  1. Brain Tumour Research charity
  2. Royal College of Surgeons of England (RCSEng)
  3. FP7 Marie Curie Actions fellowship via The CASCADE International Fellowship Program [PCOFUND-GA-2012-600181]
  4. Neuroscience
  5. German Cancer Aid [70112956]
  6. Else Kroner-Fresenius Stiftung [EKFS 2015_A60]
  7. Else Kroner Excellence Program of the Else KronerFresenius Stiftung [EKFS 2017_EKES.24]

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This study identified Fibulin-2 as a potential biomarker for grade II meningiomas, with significantly higher expression levels in grade II compared to grade I, both in tumor tissues and blood plasma. The trend of elevated Fibulin-2 in plasma suggests its potential as a non-invasive biomarker for differentiating grade II meningiomas.
There is an unmet need for the identification of biomarkers to aid in the diagnosis, clinical management, prognosis and follow-up of meningiomas. There is currently no consensus on the optimum management of WHO grade II meningiomas. In this study, we identified the calcium binding extracellular matrix glycoprotein, Fibulin-2, via mass-spectrometry-based proteomics, assessed its expression in grade I and II meningiomas and explored its potential as a grade II biomarker. A total of 87 grade I and 91 grade II different meningioma cells, tissue and plasma samples were used for the various experimental techniques employed to assess Fibulin-2 expression. The tumours were reviewed and classified according to the 2016 edition of the Classification of the Tumours of the central nervous system (CNS). Mass spectrometry proteomic analysis identified Fibulin-2 as a differentially expressed protein between grade I and II meningioma cell cultures. Fibulin-2 levels were further evaluated in meningioma cells using Western blotting and Real-time Quantitative Polymerase Chain Reaction (RT-qPCR); in meningioma tissues via immunohistochemistry and RT-qPCR; and in plasma via Enzyme-Linked Immunosorbent Assay (ELISA). Proteomic analyses (p < 0.05), Western blotting (p < 0.05) and RT-qPCR (p < 0.01) confirmed significantly higher Fibulin-2 (FBLN2) expression levels in grade II meningiomas compared to grade I. Fibulin-2 blood plasma levels were also significantly higher in grade II meningioma patients compared to grade I patients. This study suggests that elevated Fibulin-2 might be a novel grade II meningioma biomarker, when differentiating them from the grade I tumours. The trend of Fibulin-2 expression observed in plasma may serve as a useful non-invasive biomarker.

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