Evidence map›Paper›PMID 33846316›Full record

ArticleNature communications2021

The white matter is a pro-differentiative niche for glioblastoma.

Lucy J Brooks, Melanie P Clements, Jemima J Burden, Daniela Kocher, Luca Richards, Sara Castro Devesa, Leila Zakka, Megan Woodberry, Michael Ellis, Zane Jaunmuktane and 6 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 62 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 2 pooled it
7.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

62 citing papers in PubMed, 2 syntheses or guidelines pooled it, 85 citations in OpenAlex.

  1. Pooled it
  2. Predicting glioblastoma progression using MR diffusion tensor imaging: A systematic review.Journal of neuroimaging : official journal of the American Society of Neuroimaging
    Pooled it
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

2 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 7 institutions in 2 countries.

Lucy J BrooksSamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, WC1E 6DD, UK.
Melanie P ClementsSamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, WC1E 6DD, UK.ORCID http://orcid.org/0000-0001-5265-8830
Jemima J BurdenMRC Laboratory for Molecular Cell Biology, University College London, Gower Street, London, WC1E 6BT, UK.ORCID http://orcid.org/0000-0001-5894-7043
Daniela KocherSamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, WC1E 6DD, UK.
Luca RichardsSamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, WC1E 6DD, UK.
Sara Castro DevesaSamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, WC1E 6DD, UK.
Leila ZakkaSamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, WC1E 6DD, UK.
Megan WoodberrySamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, WC1E 6DD, UK.
Michael EllisSamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, WC1E 6DD, UK.
Zane JaunmuktaneDivision of Neuropathology, National Hospital for Neurology and Neurosurgery, University College London NHS Foundation Trust, Queen Square, WC1N 3BG, London, UK.
Sebastian BrandnerDivision of Neuropathology, National Hospital for Neurology and Neurosurgery, University College London NHS Foundation Trust, Queen Square, WC1N 3BG, London, UK.ORCID http://orcid.org/0000-0002-9821-0342
Gillian MorrisonMRC Centre for Regenerative Medicine and Edinburgh Cancer Research UK Cancer Centre, University of Edinburgh, 5 Little France Drive, Edinburgh, EH16 4UU, UK.
Steven M PollardMRC Centre for Regenerative Medicine and Edinburgh Cancer Research UK Cancer Centre, University of Edinburgh, 5 Little France Drive, Edinburgh, EH16 4UU, UK.ORCID http://orcid.org/0000-0001-6428-0492
Peter B DirksDivision of Neurosurgery, Arthur and Sonia Labatt Brain Tumor Research Center, Departments of Surgery and Molecular Genetics, Hospital for Sick Children, Toronto, ON, M5G 1X8, Canada.ORCID http://orcid.org/0000-0001-5718-6465
Samuel MargueratMRC London Institute of Medical Sciences, Du Cane Road, London, W12 0NN, UK.ORCID http://orcid.org/0000-0002-2402-3165
Simona ParrinelloSamantha Dickson Brain Cancer Unit, UCL Cancer Institute, London, WC1E 6DD, UK. s.parrinello@ucl.ac.uk.ORCID http://orcid.org/0000-0003-0820-6292
CRUK Lung Cancer Centre of Excellence · GBEdinburgh Cancer Research · GBNational Hospital for Neurology and Neurosurgery · GBCancer Research UK · GBHospital for Sick Children · CAMRC Laboratory for Molecular Cell Biology · GBMRC London Institute of Medical Sciences · GB

Funding

Cancer Research UK 17368Cancer Research UK 21203Cancer Research UK 21992Cancer Research UK 23459Cancer Research UK 27590Cancer Research UK 28592Cancer Research UK 28990Cancer Research UK A21992Medical Research Council G0701018Medical Research Council G1100578Medical Research Council MC-A658-5TY20Medical Research Council MC_U12266BMedical Research Council MC_UP_1102/8Medical Research Council MC_UP_A652_1002Medical Research Council MR/N004272/1
6 · The paper itself

Abstract

Glioblastomas are hierarchically organised tumours driven by glioma stem cells that retain partial differentiation potential. Glioma stem cells are maintained in specialised microenvironments, but whether, or how, they undergo lineage progression outside of these niches remains unclear. Here we identify the white matter as a differentiative niche for glioblastomas with oligodendrocyte lineage competency. Tumour cells in contact with white matter acquire pre-oligodendrocyte fate, resulting in decreased proliferation and invasion. Differentiation is a response to white matter injury, which is caused by tumour infiltration itself in a tumoursuppressive feedback loop. Mechanistically, tumour cell differentiation is driven by selective white matter upregulation of SOX10, a master regulator of normal oligodendrogenesis. SOX10 overexpression or treatment with myelination-promoting agents that upregulate endogenous SOX10, mimic this response, leading to niche-independent pre-oligodendrocyte differentiation and tumour suppression in vivo. Thus, glioblastoma recapitulates an injury response and exploiting this latent programme may offer treatment opportunities for a subset of patients.

Indexed as

Cell DifferentiationAnimalsBrain NeoplasmsCell LineageCell ProliferationDisease ProgressionFemaleGene Expression Regulation, NeoplasticGlioblastomaMiceMice, Inbred NODMice, SCIDMyelin SheathOligodendrogliaSOXE Transcription FactorsTranscriptomeSOXE Transcription Factors

Identifiers

PMID33846316
PMCPMC8042097
OpenAlexW3153793603

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.