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Correlation of in vitro infiltration with glioma histological type in organotypic brain slices

Diffuse invasion of the brain, an intrinsic property of gliomas, renders these tumours incurable, and is a principal determinant of their spatial and temporal growth. Knowledge of the invasive potential of gliomas is highly desired in order to understand their behaviour in vivo. Comprehensive ex viv...

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Autores principales: Palfi, S, Swanson, K R, de Boüard, S, Chrétien, F, Oliveira, R, Gherardi, R K, Kros, J M, Peschanski, M, Christov, C
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364801/
https://www.ncbi.nlm.nih.gov/pubmed/15292940
http://dx.doi.org/10.1038/sj.bjc.6602048
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author Palfi, S
Swanson, K R
de Boüard, S
Chrétien, F
Oliveira, R
Gherardi, R K
Kros, J M
Peschanski, M
Christov, C
author_facet Palfi, S
Swanson, K R
de Boüard, S
Chrétien, F
Oliveira, R
Gherardi, R K
Kros, J M
Peschanski, M
Christov, C
author_sort Palfi, S
collection PubMed
description Diffuse invasion of the brain, an intrinsic property of gliomas, renders these tumours incurable, and is a principal determinant of their spatial and temporal growth. Knowledge of the invasive potential of gliomas is highly desired in order to understand their behaviour in vivo. Comprehensive ex vivo invasion studies including tumours of different histological types and grades are however lacking, mostly because reliable physiological invasion assays have been difficult to establish. Using an organotypic rodent brain slice assay, we evaluated the invasiveness of 42 grade II–IV glioma biopsy specimens, and correlated it with the histological phenotype, the absence or presence of deletions on chromosomes 1p and 19q assessed by fluorescent in situ hybridisation, and proliferation and apoptosis indices assessed by immunocytochemistry. Oligodendroglial tumours with 1p/19q loss were less invasive than astrocytic tumours of similar tumour grade. Correlation analysis of invasiveness cell proliferation and apoptosis further suggested that grade II–III oligodendroglial tumours with 1p/19q loss grow in situ as relatively circumscribed compact masses in contrast to the more infiltrative and more diffuse astrocytomas. Lower invasiveness may be an important characteristic of oligodendroglial tumours, adding to our understanding of their more indolent clinical evolution and responsiveness to therapy.
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spelling pubmed-23648012009-09-10 Correlation of in vitro infiltration with glioma histological type in organotypic brain slices Palfi, S Swanson, K R de Boüard, S Chrétien, F Oliveira, R Gherardi, R K Kros, J M Peschanski, M Christov, C Br J Cancer Molecular and Cellular Pathology Diffuse invasion of the brain, an intrinsic property of gliomas, renders these tumours incurable, and is a principal determinant of their spatial and temporal growth. Knowledge of the invasive potential of gliomas is highly desired in order to understand their behaviour in vivo. Comprehensive ex vivo invasion studies including tumours of different histological types and grades are however lacking, mostly because reliable physiological invasion assays have been difficult to establish. Using an organotypic rodent brain slice assay, we evaluated the invasiveness of 42 grade II–IV glioma biopsy specimens, and correlated it with the histological phenotype, the absence or presence of deletions on chromosomes 1p and 19q assessed by fluorescent in situ hybridisation, and proliferation and apoptosis indices assessed by immunocytochemistry. Oligodendroglial tumours with 1p/19q loss were less invasive than astrocytic tumours of similar tumour grade. Correlation analysis of invasiveness cell proliferation and apoptosis further suggested that grade II–III oligodendroglial tumours with 1p/19q loss grow in situ as relatively circumscribed compact masses in contrast to the more infiltrative and more diffuse astrocytomas. Lower invasiveness may be an important characteristic of oligodendroglial tumours, adding to our understanding of their more indolent clinical evolution and responsiveness to therapy. Nature Publishing Group 2004-08-16 2004-08-03 /pmc/articles/PMC2364801/ /pubmed/15292940 http://dx.doi.org/10.1038/sj.bjc.6602048 Text en Copyright © 2004 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular and Cellular Pathology
Palfi, S
Swanson, K R
de Boüard, S
Chrétien, F
Oliveira, R
Gherardi, R K
Kros, J M
Peschanski, M
Christov, C
Correlation of in vitro infiltration with glioma histological type in organotypic brain slices
title Correlation of in vitro infiltration with glioma histological type in organotypic brain slices
title_full Correlation of in vitro infiltration with glioma histological type in organotypic brain slices
title_fullStr Correlation of in vitro infiltration with glioma histological type in organotypic brain slices
title_full_unstemmed Correlation of in vitro infiltration with glioma histological type in organotypic brain slices
title_short Correlation of in vitro infiltration with glioma histological type in organotypic brain slices
title_sort correlation of in vitro infiltration with glioma histological type in organotypic brain slices
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364801/
https://www.ncbi.nlm.nih.gov/pubmed/15292940
http://dx.doi.org/10.1038/sj.bjc.6602048
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