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Model glioma heterogeneity, progression and treatment response with confidence

Introduction

Well‑characterised, patient‑derived glioma models capturing tumour cell states, disease progression and clinically relevant diversity

Glioma research demands models that reflect tumour heterogeneity, cellular state and disease progression. Our brain cancer portfolio enables researchers to:

  • Interrogate glioblastoma heterogeneity and cell states using glioma stem cell models with deep molecular characterisation 
  • Compare clinically relevant disease contexts with patient‑derived models spanning primary and relapse glioblastoma 
  • Model tumour evolution and progression using IDHmutant glioma models representing low-grade disease state 

All models are built by leading cancer experts and global institutes, with traceable origins – giving you confidence in research integrity and reproducibility.

Feature brain cancer models

Human | Glioblastoma stem-like models (IDH-wildtype)

Developed by Steven Pollard, Gillian Morrison (University of Edinburgh)

Interrogate glioblastoma heterogeneity and transcriptional cell states using deeply characterised, patient‑derived glioma stem cell models.

GCGR E55 ICC SOX2 and NESTIN, at x20

Key features

  • Deep molecular characterisation including transcriptomic, genomic and DNA methylation profiling, capturing glioblastoma transcriptional states across established frameworks 
  • Patient‑derived glioma stem cell models that retain tumour heterogeneity and stem‑like characteristics 
  • Grown as adherent, laminin‑dependent monolayers, enabling consistent and scalable experimental workflows 

Applications

  • Compare treatment response across molecular subtypes 
  • Screen compounds and identify candidate hits in vitro and in vivo  
  • Investigate how stem‑like cell states influence tumour progression 

Discover the GCGR cell lines

Tool nameCat. #Inventor/ InstituteOrganismKey attributes
GCGR-E43 140075Steven Pollard, Gillian Morrison University of Edinburgh Human– Classical GBM line,
– Part of a panel of patient-derived glioma stem cell lines
GCGR-E63140084 Steven Pollard, Gillian Morrison University of Edinburgh Human– Classical GBM line,
– Part of a panel of patient-derived glioma stem cell lines
GCGR-E20 140061 Steven Pollard, Gillian Morrison University of Edinburgh Human– Proneural GBM line,
– Part of a panel of patient-derived glioma stem cell lines
GCGR-E53 140077 Steven Pollard, Gillian Morrison University of Edinburgh Human– Proneural GBM line,
– Part of a panel of patient-derived glioma stem cell lines
GCGR-E55 140079 Steven Pollard, Gillian Morrison University of Edinburgh Human– Mesenchymal GBM line,
– Part of a panel of patient-derived glioma stem cell lines
GCGR-E57 140081 Steven Pollard, Gillian Morrison University of Edinburgh Human– Mesenchymal GBM line,
– Part of a panel of patient-derived glioma stem cell lines

Human | Glioma models (Heidelberg collection)

Developed by Christel Herold-Mende (University of Heidelberg)

Model glioma initiation, progression, and transition to high‑grade disease using patient‑derived IDH‑mutant glioma stem‑like cell lines.

IDHmut glioma stem-like NCH551b cell line
IDHmut glioma stem-like NCH551b cell line

High-Grade Glioblastoma models (IDH-Wildtype)

Key features
  • Derived from primary and relapsed WHO grade IV glioblastoma tumours 
  • Represents the major molecular subtypes and MGMT promoter states 
  • Models from both primary tumours and relapse models
Applications
  • Model relapse and therapy resistance 
  • Compare treatment response across glioblastoma models and molecular subtypes 
Discover the high grade glioblastoma models
Tool nameCat. #Inventor/ InstituteOrganismKey attributes
NCH57162334 Christel Herold-Mende
University of Heidelberg 
HumanRare Gliosarcoma model 
NCH1425 162333 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
NCH741f162332 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
NCH711d162331 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
NCH705162330 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
NCH669162329 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
NCH663 162328 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
NCH660h162327 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
NCH627162326 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
 NCH601 162325 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
NCH592b162324 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
NCH588j162323 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
NCH481162322 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
NCH465162321 Christel Herold-Mende
University of Heidelberg 
HumanNeurosphere models of Glioblastoma 
NCH676162320 Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH474162319 Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH453162318 Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH417162317 Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH354162316 Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH343162315 Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH342162314 Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH270162313Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH210162312Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH156162311Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH149162310Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH125162309Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH89162308Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH82162306Christel Herold-Mende
University of Heidelberg 
HumanAdherent Glioblastoma models 
NCH93162305 Christel Herold-Mende
University of Heidelberg 
HumanRare Meningioma model with deleterious NF2 frameshift deletion, missense ALK and PTCH1 mutation 

Low grade glioma models (IDHmutant astrocytoma)

Key features
  • Derived from astrocytoma relapse samples, reflecting tumour evolution from lower‑grade disease 
  • IDH‑mutant background with defined MGMT and BRAF status reported in primary tumours 
  • Maintained as neurosphere cultures under serum‑free conditions 
Applications
  • Model progression from low‑grade glioma 
  • Investigate how IDH mutation status shapes tumour biology 
Discover the IDH mutant low grade cell lines
Tool nameCat. #Inventor/ InstituteOrganismKey attributes
NCH3763162307 Christel Herold-Mende
University of Heidelberg 
HumanLow-grade Glioma models, IDHmutant Astrocytoma relapse models 
NCH1681162304 Christel Herold-Mende
University of Heidelberg 
HumanLow-grade Glioma models, IDHmutant Astrocytoma relapse models 
NCH645162303 Christel Herold-Mende
University of Heidelberg 
HumanLow-grade Glioma models, IDHmutant Astrocytoma relapse models 
NCH620162302 Christel Herold-Mende
University of Heidelberg 
HumanLow-grade Glioma models, IDHmutant Astrocytoma relapse models 
NCH551b162301 Christel Herold-Mende
University of Heidelberg 
HumanLow-grade Glioma models, IDHmutant Astrocytoma relapse models 

Discover more brain cancer tools

Tool nameCat. #Inventor/ InstituteOrganismKey attributes
NCH57162334 Christel Herold-Mende
University of Heidelberg 
HumanRare Gliosarcoma model 
NCH93162305 Christel Herold-Mende
University of Heidelberg 
HumanRare Meningioma model with deleterious NF2 frameshift deletion, missense ALK and PTCH1 mutation 

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