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Multiparametric magnetic resonance in the assessment of the gender differences in a high-grade glioma rat model

BACKGROUND: Glioblastoma, the most frequent and aggressive of all astrocytomas, presents a clear predominance in male humans, but the assessment of sexual differences in its tumourigenesis and growth has received little attention so far. In this study, we aim to identify gender-dependent surrogate m...

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Autores principales: Pérez-Carro, Rocío, Cauli, Omar, López-Larrubia, Pilar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452640/
https://www.ncbi.nlm.nih.gov/pubmed/26116110
http://dx.doi.org/10.1186/s13550-014-0044-4
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author Pérez-Carro, Rocío
Cauli, Omar
López-Larrubia, Pilar
author_facet Pérez-Carro, Rocío
Cauli, Omar
López-Larrubia, Pilar
author_sort Pérez-Carro, Rocío
collection PubMed
description BACKGROUND: Glioblastoma, the most frequent and aggressive of all astrocytomas, presents a clear predominance in male humans, but the assessment of sexual differences in its tumourigenesis and growth has received little attention so far. In this study, we aim to identify gender-dependent surrogate markers in an animal model of this cancer by means of magnetic resonance (MR) imaging and biochemical and behavioural studies. METHODS: A high-grade glioma model developed in male and female rats was used. Multiparametric magnetic resonance images and localized spectra were acquired. The MR parameters linked to tumoural features were quantified. Motor and metabolic activity was also assessed. Postmortem analyses were carried out to measure indicators of malignancy, tumoural metabolism and viability of the blood-brain barrier (BBB). RESULTS: Statistically significant differences dependent on the animal sex were found in the study of pathological indicators like oedema, inflammation, cellularity and microvasculature. Results suggest higher cell proliferative rate, inflammation and vasogenic oedema and or necrosis in glioma-bearing male rats. Haemodynamic parameters measured indicated a major disruption of the BBB, postmortem confirmed, in this sex. Metabolomic and energetic metabolism activity data are in agreement with a major malignancy and aggressiveness of this cancer model on males. CONCLUSIONS: Gender differences should be taken into account in preclinical studies of glioblastoma models, in the characterization of the tumoural behaviour and consequently in the development and validation of new therapeutic approaches. MR imaging and spectroscopy allow to non-invasively monitor this sexual dimorphism in the diagnosis and prognosis of brain cancer.
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spelling pubmed-44526402015-06-09 Multiparametric magnetic resonance in the assessment of the gender differences in a high-grade glioma rat model Pérez-Carro, Rocío Cauli, Omar López-Larrubia, Pilar EJNMMI Res Original Research BACKGROUND: Glioblastoma, the most frequent and aggressive of all astrocytomas, presents a clear predominance in male humans, but the assessment of sexual differences in its tumourigenesis and growth has received little attention so far. In this study, we aim to identify gender-dependent surrogate markers in an animal model of this cancer by means of magnetic resonance (MR) imaging and biochemical and behavioural studies. METHODS: A high-grade glioma model developed in male and female rats was used. Multiparametric magnetic resonance images and localized spectra were acquired. The MR parameters linked to tumoural features were quantified. Motor and metabolic activity was also assessed. Postmortem analyses were carried out to measure indicators of malignancy, tumoural metabolism and viability of the blood-brain barrier (BBB). RESULTS: Statistically significant differences dependent on the animal sex were found in the study of pathological indicators like oedema, inflammation, cellularity and microvasculature. Results suggest higher cell proliferative rate, inflammation and vasogenic oedema and or necrosis in glioma-bearing male rats. Haemodynamic parameters measured indicated a major disruption of the BBB, postmortem confirmed, in this sex. Metabolomic and energetic metabolism activity data are in agreement with a major malignancy and aggressiveness of this cancer model on males. CONCLUSIONS: Gender differences should be taken into account in preclinical studies of glioblastoma models, in the characterization of the tumoural behaviour and consequently in the development and validation of new therapeutic approaches. MR imaging and spectroscopy allow to non-invasively monitor this sexual dimorphism in the diagnosis and prognosis of brain cancer. Springer Berlin Heidelberg 2014-09-09 /pmc/articles/PMC4452640/ /pubmed/26116110 http://dx.doi.org/10.1186/s13550-014-0044-4 Text en © Pérez-Carro et al.; licensee Springer. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Original Research
Pérez-Carro, Rocío
Cauli, Omar
López-Larrubia, Pilar
Multiparametric magnetic resonance in the assessment of the gender differences in a high-grade glioma rat model
title Multiparametric magnetic resonance in the assessment of the gender differences in a high-grade glioma rat model
title_full Multiparametric magnetic resonance in the assessment of the gender differences in a high-grade glioma rat model
title_fullStr Multiparametric magnetic resonance in the assessment of the gender differences in a high-grade glioma rat model
title_full_unstemmed Multiparametric magnetic resonance in the assessment of the gender differences in a high-grade glioma rat model
title_short Multiparametric magnetic resonance in the assessment of the gender differences in a high-grade glioma rat model
title_sort multiparametric magnetic resonance in the assessment of the gender differences in a high-grade glioma rat model
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452640/
https://www.ncbi.nlm.nih.gov/pubmed/26116110
http://dx.doi.org/10.1186/s13550-014-0044-4
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