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Diffusion Kurtosis Imaging Reflects Glial Fibrillary Acidic Protein (GFAP), Topo IIα, and O(6)-Methylguanine-DNA Methyltransferase (MGMT) Expression in Astrocytomas

BACKGROUND: Astrocytomas are the most common primary brain neoplasms. Biological indicators of astrocytomas can reflect its biological characteristics. The aim of this study was to assess the expression of the pathological glial fibrillary acidic protein (GFAP) Topo IIα and O(6)-methylguanine-DNA me...

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Autores principales: Wang, Xiao-chun, Lei, Ying, Wang, Le, Tan, Yan, Qin, Jiang-bo, Ma, Guo-lin, Zhang, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292149/
https://www.ncbi.nlm.nih.gov/pubmed/30520434
http://dx.doi.org/10.12659/MSM.911631
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author Wang, Xiao-chun
Lei, Ying
Wang, Le
Tan, Yan
Qin, Jiang-bo
Ma, Guo-lin
Zhang, Hui
author_facet Wang, Xiao-chun
Lei, Ying
Wang, Le
Tan, Yan
Qin, Jiang-bo
Ma, Guo-lin
Zhang, Hui
author_sort Wang, Xiao-chun
collection PubMed
description BACKGROUND: Astrocytomas are the most common primary brain neoplasms. Biological indicators of astrocytomas can reflect its biological characteristics. The aim of this study was to assess the expression of the pathological glial fibrillary acidic protein (GFAP) Topo IIα and O(6)-methylguanine-DNA methyltransferase (MGMT) in astrocytomas using magnetic resonance (MR) diffusion kurtosis imaging (DKI) to evaluate the biological characteristics of astrocytomas. MATERIAL/METHODS: Sixty-six patients with pathologically proven astrocytomas were enrolled in this study. All patients underwent conventional MRI head scanning, DKI scanning, and enhanced scanning under the same conditions. Spearman’s rank correlation analysis and Bonferroni correction were used to compare the values of DKI and the expression levels of GFAP, Topo IIα, and MGMT between the 2 groups. RESULTS: Mean kurtosis (MK) values were negatively correlated with the expression of GFAP (r=−0.836; P=0.03). However, these were positively correlated with the expression of Topo IIα (r=0.896; P=0.01). Moreover, fractional anisotropy (FA) values were not correlated with the expression of GFAP (r=0.366; P=0.05), Topo IIα (r=−0.562; P=0.05), or MGMT (r=−0.153; P=0.10). CONCLUSIONS: MK was significantly associated with the expression of GFAP and Topo IIα. To a certain extent, applying DKI may show the biological behavior of tumor cell differentiation, proliferation activity, invasion, and metastasis, and guide individual treatment.
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spelling pubmed-62921492019-01-03 Diffusion Kurtosis Imaging Reflects Glial Fibrillary Acidic Protein (GFAP), Topo IIα, and O(6)-Methylguanine-DNA Methyltransferase (MGMT) Expression in Astrocytomas Wang, Xiao-chun Lei, Ying Wang, Le Tan, Yan Qin, Jiang-bo Ma, Guo-lin Zhang, Hui Med Sci Monit Clinical Research BACKGROUND: Astrocytomas are the most common primary brain neoplasms. Biological indicators of astrocytomas can reflect its biological characteristics. The aim of this study was to assess the expression of the pathological glial fibrillary acidic protein (GFAP) Topo IIα and O(6)-methylguanine-DNA methyltransferase (MGMT) in astrocytomas using magnetic resonance (MR) diffusion kurtosis imaging (DKI) to evaluate the biological characteristics of astrocytomas. MATERIAL/METHODS: Sixty-six patients with pathologically proven astrocytomas were enrolled in this study. All patients underwent conventional MRI head scanning, DKI scanning, and enhanced scanning under the same conditions. Spearman’s rank correlation analysis and Bonferroni correction were used to compare the values of DKI and the expression levels of GFAP, Topo IIα, and MGMT between the 2 groups. RESULTS: Mean kurtosis (MK) values were negatively correlated with the expression of GFAP (r=−0.836; P=0.03). However, these were positively correlated with the expression of Topo IIα (r=0.896; P=0.01). Moreover, fractional anisotropy (FA) values were not correlated with the expression of GFAP (r=0.366; P=0.05), Topo IIα (r=−0.562; P=0.05), or MGMT (r=−0.153; P=0.10). CONCLUSIONS: MK was significantly associated with the expression of GFAP and Topo IIα. To a certain extent, applying DKI may show the biological behavior of tumor cell differentiation, proliferation activity, invasion, and metastasis, and guide individual treatment. International Scientific Literature, Inc. 2018-12-06 /pmc/articles/PMC6292149/ /pubmed/30520434 http://dx.doi.org/10.12659/MSM.911631 Text en © Med Sci Monit, 2018 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Clinical Research
Wang, Xiao-chun
Lei, Ying
Wang, Le
Tan, Yan
Qin, Jiang-bo
Ma, Guo-lin
Zhang, Hui
Diffusion Kurtosis Imaging Reflects Glial Fibrillary Acidic Protein (GFAP), Topo IIα, and O(6)-Methylguanine-DNA Methyltransferase (MGMT) Expression in Astrocytomas
title Diffusion Kurtosis Imaging Reflects Glial Fibrillary Acidic Protein (GFAP), Topo IIα, and O(6)-Methylguanine-DNA Methyltransferase (MGMT) Expression in Astrocytomas
title_full Diffusion Kurtosis Imaging Reflects Glial Fibrillary Acidic Protein (GFAP), Topo IIα, and O(6)-Methylguanine-DNA Methyltransferase (MGMT) Expression in Astrocytomas
title_fullStr Diffusion Kurtosis Imaging Reflects Glial Fibrillary Acidic Protein (GFAP), Topo IIα, and O(6)-Methylguanine-DNA Methyltransferase (MGMT) Expression in Astrocytomas
title_full_unstemmed Diffusion Kurtosis Imaging Reflects Glial Fibrillary Acidic Protein (GFAP), Topo IIα, and O(6)-Methylguanine-DNA Methyltransferase (MGMT) Expression in Astrocytomas
title_short Diffusion Kurtosis Imaging Reflects Glial Fibrillary Acidic Protein (GFAP), Topo IIα, and O(6)-Methylguanine-DNA Methyltransferase (MGMT) Expression in Astrocytomas
title_sort diffusion kurtosis imaging reflects glial fibrillary acidic protein (gfap), topo iiα, and o(6)-methylguanine-dna methyltransferase (mgmt) expression in astrocytomas
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292149/
https://www.ncbi.nlm.nih.gov/pubmed/30520434
http://dx.doi.org/10.12659/MSM.911631
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