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Anatomical specificity of vascular endothelial growth factor expression in glioblastomas: a voxel-based mapping analysis.

Authors :
Wang, Yinyan
Jiang, Tao
Fan, Xing
Wang, Kai
Ma, Jun
Li, Shaowu
Liu, Shuai
Liu, Yong
Source :
Neuroradiology; Jan2016, Vol. 58 Issue 1, p69-75, 7p
Publication Year :
2016

Abstract

Introduction: The expression of vascular endothelial growth factor (VEGF) is a common genetic alteration in malignant gliomas and contributes to the angiogenesis of tumors. This study aimed to investigate the anatomical specificity of VEGF expression levels in glioblastomas using voxel-based neuroimaging analysis. Methods: Clinical information, MR scans, and immunohistochemistry stains of 209 patients with glioblastomas were reviewed. All tumor lesions were segmented manually and subsequently registered to standard brain space. Voxel-based regression analysis was performed to correlate the brain regions of tumor involvement with the level of VEGF expression. Brain regions identified as significantly associated with high or low VEGF expression were preserved following permutation correction. Results: High VEGF expression was detected in 123 (58.9 %) of the 209 patients. Voxel-based statistical analysis demonstrated that high VEGF expression was more likely in tumors located in the left frontal lobe and the right caudate and low VEGF expression was more likely in tumors that occurred in the posterior region of the right lateral ventricle. Conclusion: Voxel-based neuroimaging analysis revealed the anatomic specificity of VEGF expression in glioblastoma, which may further our understanding of genetic heterogeneity during tumor origination. This finding provides primary theoretical support for potential future application of customized antiangiogenic therapy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00283940
Volume :
58
Issue :
1
Database :
Complementary Index
Journal :
Neuroradiology
Publication Type :
Academic Journal
Accession number :
112455355
Full Text :
https://doi.org/10.1007/s00234-015-1602-9