Modelling the microenvironment of the most aggressive brain tumours for preclinical studies

Preclinical and clinical cancer studies use unrepresentative tumour models that do not properly simulate the intricate pathobiology of the human tumour and its complex microenvironment. This is of critical importance for the brain tumour glioblastoma (GBM), one of the most malignant cancers, which a...

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Autores principales: Juš Žavbi, Barbara Breznik
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/13d8abdaf9e9438f97142dd7ee21fff8
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spelling oai:doaj.org-article:13d8abdaf9e9438f97142dd7ee21fff82021-11-28T04:40:11ZModelling the microenvironment of the most aggressive brain tumours for preclinical studies2667-394010.1016/j.adcanc.2021.100017https://doaj.org/article/13d8abdaf9e9438f97142dd7ee21fff82021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2667394021000174https://doaj.org/toc/2667-3940Preclinical and clinical cancer studies use unrepresentative tumour models that do not properly simulate the intricate pathobiology of the human tumour and its complex microenvironment. This is of critical importance for the brain tumour glioblastoma (GBM), one of the most malignant cancers, which almost always relapses despite treatment. Due to the intertumoral and intratumoral heterogeneity of GBM, it is highly resistant to conventional treatment with radiotherapy and chemotherapy. In this review, we describe the heterogeneity of GBM and the unique microenvironment of brain tumours as well as their importance for GBM progression and to set up clinically relevant GBM models for successful preclinical research and drug screening. A combination of cancer cells, cancer stem cells, and cancer-associated cells create an intricate and diverse tumour microenvironment. GBM is very adept at recruiting healthy cells to support itself. The function of these cancer-associated cells varies in different niches, but they all share the common function of promoting tumour growth and spread. Glioblastoma stem cells are one of the central components of GBM treatment resistance, invasiveness, and cancer stem cell niche relationships. All of these aspects are critical when selecting and designing preclinical GBM models.Juš ŽavbiBarbara BreznikElsevierarticleBrain cancerGlioblastomaTumour microenvironmentTumour modelsCancer stem cellsTherapyNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENAdvances in Cancer Biology - Metastasis, Vol 3, Iss , Pp 100017- (2021)
institution DOAJ
collection DOAJ
language EN
topic Brain cancer
Glioblastoma
Tumour microenvironment
Tumour models
Cancer stem cells
Therapy
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle Brain cancer
Glioblastoma
Tumour microenvironment
Tumour models
Cancer stem cells
Therapy
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Juš Žavbi
Barbara Breznik
Modelling the microenvironment of the most aggressive brain tumours for preclinical studies
description Preclinical and clinical cancer studies use unrepresentative tumour models that do not properly simulate the intricate pathobiology of the human tumour and its complex microenvironment. This is of critical importance for the brain tumour glioblastoma (GBM), one of the most malignant cancers, which almost always relapses despite treatment. Due to the intertumoral and intratumoral heterogeneity of GBM, it is highly resistant to conventional treatment with radiotherapy and chemotherapy. In this review, we describe the heterogeneity of GBM and the unique microenvironment of brain tumours as well as their importance for GBM progression and to set up clinically relevant GBM models for successful preclinical research and drug screening. A combination of cancer cells, cancer stem cells, and cancer-associated cells create an intricate and diverse tumour microenvironment. GBM is very adept at recruiting healthy cells to support itself. The function of these cancer-associated cells varies in different niches, but they all share the common function of promoting tumour growth and spread. Glioblastoma stem cells are one of the central components of GBM treatment resistance, invasiveness, and cancer stem cell niche relationships. All of these aspects are critical when selecting and designing preclinical GBM models.
format article
author Juš Žavbi
Barbara Breznik
author_facet Juš Žavbi
Barbara Breznik
author_sort Juš Žavbi
title Modelling the microenvironment of the most aggressive brain tumours for preclinical studies
title_short Modelling the microenvironment of the most aggressive brain tumours for preclinical studies
title_full Modelling the microenvironment of the most aggressive brain tumours for preclinical studies
title_fullStr Modelling the microenvironment of the most aggressive brain tumours for preclinical studies
title_full_unstemmed Modelling the microenvironment of the most aggressive brain tumours for preclinical studies
title_sort modelling the microenvironment of the most aggressive brain tumours for preclinical studies
publisher Elsevier
publishDate 2021
url https://doaj.org/article/13d8abdaf9e9438f97142dd7ee21fff8
work_keys_str_mv AT juszavbi modellingthemicroenvironmentofthemostaggressivebraintumoursforpreclinicalstudies
AT barbarabreznik modellingthemicroenvironmentofthemostaggressivebraintumoursforpreclinicalstudies
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