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FXYD2 mRNA expression represents a new independent factor that affects survival of glioma patients and predicts chemosensitivity of patients to temozolomide.

Authors :
Zhou K
Jiang T
Liu Y
Zhao Z
Huang L
Li G
Source :
BMC neurology [BMC Neurol] 2021 Nov 09; Vol. 21 (1), pp. 438. Date of Electronic Publication: 2021 Nov 09.
Publication Year :
2021

Abstract

Purpose: Glioma is the most common primary intracranial tumor. Owing to the poor prognosis associated with high-grade gliomas, there is an urgent need to identify biomarkers related to prognosis and treatment sensitivity. Here, we analyze the expression of FXYD2 mRNA in gliomas, and explore its clinical prognostic value and significance in this disease.<br />Methods: Clinical features, FXYD2 mRNA expression levels, and survival data were analyzed for 516 glioma patients from the Chinese Glioma Genome Map Project, 481 from the cancer genome map datbase and 268 from the molecular braintumor database. The expression patterns for FXYD2 mRNA were compared using the chi-square test, and overall survival (OS) of glioma patients was evaluated according to FXYD2 mRNA expression levels. The factors affecting glioma survival were evaluated by Cox univariate and multivariate regression analysis.<br />Results: FXYD2 mRNA expression was related to the grade of gliomas. The higher the level, the lower the expression. Meanwhile related to the pathological classification of gliomas. Oligodendroglioma, IDH-mutant and 1p/19q-codeleted was higher than Astrocytoma, IDH-mutant, higher than Glioblastoma, IDH-wildtype. Moreover, temozolomide (TMZ) chemotherapy was found to be an independent factor affecting survival in patients with high FXYD2 mRNA expression, but not in patients with low expression.<br />Conclusion: FXYD2 mRNA expression represents a new independent factor affecting the survival of glioma patients and may serve as an independent prognostic indicator to predict the sensitivity of gliomas to TMZ.<br /> (© 2021. The Author(s).)

Details

Language :
English
ISSN :
1471-2377
Volume :
21
Issue :
1
Database :
MEDLINE
Journal :
BMC neurology
Publication Type :
Academic Journal
Accession number :
34753441
Full Text :
https://doi.org/10.1186/s12883-021-02476-2