Experimental models and tools to tackle glioblastoma

Glioblastoma multiforme (GBM) is one of the deadliest human cancers. Despite increasing knowledge of the genetic and epigenetic changes that underlie tumour initiation and growth, the prognosis for GBM patients remains dismal. Genome analysis has failed to lead to success in the clinic. Fresh approa...

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Main Authors: Faye L. Robertson, Maria-Angeles Marqués-Torrejón, Gillian M. Morrison, Steven M. Pollard
Format: Article
Language:English
Published: The Company of Biologists 2019-09-01
Series:Disease Models & Mechanisms
Subjects:
GBM
Online Access:http://dmm.biologists.org/content/12/9/dmm040386
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spelling doaj-2f0af0cc4e19485789cf5ad886d4c2d92020-11-25T02:32:07ZengThe Company of BiologistsDisease Models & Mechanisms1754-84031754-84112019-09-0112910.1242/dmm.040386040386Experimental models and tools to tackle glioblastomaFaye L. Robertson0Maria-Angeles Marqués-Torrejón1Gillian M. Morrison2Steven M. Pollard3 MRC Centre for Regenerative Medicine and Edinburgh Cancer Research UK Cancer Centre, University of Edinburgh, 5 Little France Drive, Edinburgh EH16 4UU, UK MRC Centre for Regenerative Medicine and Edinburgh Cancer Research UK Cancer Centre, University of Edinburgh, 5 Little France Drive, Edinburgh EH16 4UU, UK MRC Centre for Regenerative Medicine and Edinburgh Cancer Research UK Cancer Centre, University of Edinburgh, 5 Little France Drive, Edinburgh EH16 4UU, UK MRC Centre for Regenerative Medicine and Edinburgh Cancer Research UK Cancer Centre, University of Edinburgh, 5 Little France Drive, Edinburgh EH16 4UU, UK Glioblastoma multiforme (GBM) is one of the deadliest human cancers. Despite increasing knowledge of the genetic and epigenetic changes that underlie tumour initiation and growth, the prognosis for GBM patients remains dismal. Genome analysis has failed to lead to success in the clinic. Fresh approaches are needed that can stimulate new discoveries across all levels: cell-intrinsic mechanisms (transcriptional/epigenetic and metabolic), cell-cell signalling, niche and microenvironment, systemic signals, immune regulation, and tissue-level physical forces. GBMs are inherently extremely challenging: tumour detection occurs too late, and cells infiltrate widely, hiding in quiescent states behind the blood-brain barrier. The complexity of the brain tissue also provides varied and complex microenvironments that direct cancer cell fates. Phenotypic heterogeneity is therefore superimposed onto pervasive genetic heterogeneity. Despite this bleak outlook, there are reasons for optimism. A myriad of complementary, and increasingly sophisticated, experimental approaches can now be used across the research pipeline, from simple reductionist models devised to delineate molecular and cellular mechanisms, to complex animal models required for preclinical testing of new therapeutic approaches. No single model can cover the breadth of unresolved questions. This Review therefore aims to guide investigators in choosing the right model for their question. We also discuss the recent convergence of two key technologies: human stem cell and cancer stem cell culture, as well as CRISPR/Cas tools for precise genome manipulations. New functional genetic approaches in tailored models will likely fuel new discoveries, new target identification and new therapeutic strategies to tackle GBM.http://dmm.biologists.org/content/12/9/dmm040386Central nervous systemIn vitroCRISPR/Cas9MouseHumanXenograftGBMCancerBrain tumour
collection DOAJ
language English
format Article
sources DOAJ
author Faye L. Robertson
Maria-Angeles Marqués-Torrejón
Gillian M. Morrison
Steven M. Pollard
spellingShingle Faye L. Robertson
Maria-Angeles Marqués-Torrejón
Gillian M. Morrison
Steven M. Pollard
Experimental models and tools to tackle glioblastoma
Disease Models & Mechanisms
Central nervous system
In vitro
CRISPR/Cas9
Mouse
Human
Xenograft
GBM
Cancer
Brain tumour
author_facet Faye L. Robertson
Maria-Angeles Marqués-Torrejón
Gillian M. Morrison
Steven M. Pollard
author_sort Faye L. Robertson
title Experimental models and tools to tackle glioblastoma
title_short Experimental models and tools to tackle glioblastoma
title_full Experimental models and tools to tackle glioblastoma
title_fullStr Experimental models and tools to tackle glioblastoma
title_full_unstemmed Experimental models and tools to tackle glioblastoma
title_sort experimental models and tools to tackle glioblastoma
publisher The Company of Biologists
series Disease Models & Mechanisms
issn 1754-8403
1754-8411
publishDate 2019-09-01
description Glioblastoma multiforme (GBM) is one of the deadliest human cancers. Despite increasing knowledge of the genetic and epigenetic changes that underlie tumour initiation and growth, the prognosis for GBM patients remains dismal. Genome analysis has failed to lead to success in the clinic. Fresh approaches are needed that can stimulate new discoveries across all levels: cell-intrinsic mechanisms (transcriptional/epigenetic and metabolic), cell-cell signalling, niche and microenvironment, systemic signals, immune regulation, and tissue-level physical forces. GBMs are inherently extremely challenging: tumour detection occurs too late, and cells infiltrate widely, hiding in quiescent states behind the blood-brain barrier. The complexity of the brain tissue also provides varied and complex microenvironments that direct cancer cell fates. Phenotypic heterogeneity is therefore superimposed onto pervasive genetic heterogeneity. Despite this bleak outlook, there are reasons for optimism. A myriad of complementary, and increasingly sophisticated, experimental approaches can now be used across the research pipeline, from simple reductionist models devised to delineate molecular and cellular mechanisms, to complex animal models required for preclinical testing of new therapeutic approaches. No single model can cover the breadth of unresolved questions. This Review therefore aims to guide investigators in choosing the right model for their question. We also discuss the recent convergence of two key technologies: human stem cell and cancer stem cell culture, as well as CRISPR/Cas tools for precise genome manipulations. New functional genetic approaches in tailored models will likely fuel new discoveries, new target identification and new therapeutic strategies to tackle GBM.
topic Central nervous system
In vitro
CRISPR/Cas9
Mouse
Human
Xenograft
GBM
Cancer
Brain tumour
url http://dmm.biologists.org/content/12/9/dmm040386
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