Evidence map›Paper›PMID 28497778›Full record

ArticleNature communications2017

PTEN regulates glioblastoma oncogenesis through chromatin-associated complexes of DAXX and histone H3.3.

Jorge A Benitez, Jianhui Ma, Matteo D'Antonio, Antonia Boyer, Maria Fernanda Camargo, Ciro Zanca, Stephen Kelly, Alireza Khodadadi-Jamayran, Nathan M Jameson, Michael Andersen and 5 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. 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 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
7.5field-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

86 citing papers in PubMed, 145 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Cell death in glioblastoma and the central nervous system.Cellular oncology (Dordrecht, Netherlands) · 2025
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 2 countries.

Jorge A BenitezLudwig Institute for Cancer Research, La Jolla, California 92093-0660, USA.
Jianhui MaLudwig Institute for Cancer Research, La Jolla, California 92093-0660, USA.
Matteo D'AntonioThe Moores Cancer Center, University of California San Diego, La Jolla, California 92093, USA.
Antonia BoyerLudwig Institute for Cancer Research, La Jolla, California 92093-0660, USA.
Maria Fernanda CamargoThe Moores Cancer Center, University of California San Diego, La Jolla, California 92093, USA.
Ciro ZancaLudwig Institute for Cancer Research, La Jolla, California 92093-0660, USA.
Stephen KellyDepartment of Pathology, Laura &Isaac Perlmutter Cancer Center, and The Helen L. and Martin S. Kimmel Center for Stem Cell Biology, NYU School of Medicine, New York, New York 10016, USA.
Alireza Khodadadi-JamayranDepartment of Pathology, Laura &Isaac Perlmutter Cancer Center, and The Helen L. and Martin S. Kimmel Center for Stem Cell Biology, NYU School of Medicine, New York, New York 10016, USA.
Nathan M JamesonLudwig Institute for Cancer Research, La Jolla, California 92093-0660, USA.
Michael AndersenDepartment of Pathology, Haukeland University Hospital, 5021 Bergen, Norway.
Hrvoje MileticDepartment of Pathology, Haukeland University Hospital, 5021 Bergen, Norway.
Shahram SaberiDepartment of Neurosciences, University of California, San Diego, La Jolla, California 92093, USA.
Kelly A FrazerThe Moores Cancer Center, University of California San Diego, La Jolla, California 92093, USA.
Webster K CaveneeLudwig Institute for Cancer Research, La Jolla, California 92093-0660, USA.
Frank B FurnariLudwig Institute for Cancer Research, La Jolla, California 92093-0660, USA.
Ludwig Cancer Research · USUniversity of California, San Diego · USHaukeland University Hospital · NORady Children's Hospital-San Diego · USNew York University · USNYU Langone’s Laura and Isaac Perlmutter Cancer Center

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Transgenic & Knock-out MouseP30DK063491 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PETER J TONTONOZ · 2003 to 2026
$40.4M
U of Calif, San Diego Neuroscience Microscopy ImagingP30NS047101 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GLEESON, JOSEPH G, ZHENG, BINHAI · 2003 to 2022
$9.0M
Predoctoral and Postdoctoral Training in Cancer Cell BiologyT32CA067754 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JEAN Y.J. WANG · 1995 to 2026
$6.5M
Genotypic Interactions in Brain Cancer HeterogeneityR01NS080939 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FURNARI, FRANK · 2012 to 2022
$3.5M
NCI NIH HHS P30 CA016087NCI NIH HHS T32 CA067754NIDDK NIH HHS P30 DK063491NINDS NIH HHS P30 NS047101NINDS NIH HHS R01 NS080939
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most lethal type of human brain cancer, where deletions and mutations in the tumour suppressor gene PTEN (phosphatase and tensin homolog) are frequent events and are associated with therapeutic resistance. Herein, we report a novel chromatin-associated function of PTEN in complex with the histone chaperone DAXX and the histone variant H3.3. We show that PTEN interacts with DAXX and, in turn PTEN directly regulates oncogene expression by modulating DAXX-H3.3 association on the chromatin, independently of PTEN enzymatic activity. Furthermore, DAXX inhibition specifically suppresses tumour growth and improves the survival of orthotopically engrafted mice implanted with human PTEN-deficient glioma samples, associated with global H3.3 genomic distribution changes leading to upregulation of tumour suppressor genes and downregulation of oncogenes. Moreover, DAXX expression anti-correlates with PTEN expression in GBM patient samples. Since loss of chromosome 10 and PTEN are common events in cancer, this synthetic growth defect mediated by DAXX suppression represents a therapeutic opportunity to inhibit tumorigenesis specifically in the context of PTEN deletion.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCarcinogenesisCell Line, TumorCells, CulturedChromatinCo-Repressor ProteinsGlioblastomaHEK293 CellsHistonesHumansMiceMolecular ChaperonesNuclear ProteinsProtein BindingPTEN PhosphohydrolaseAdaptor Proteins, Signal TransducingChromatinCo-Repressor ProteinsDAXX protein, humanHistonesMolecular ChaperonesNuclear ProteinsPTEN PhosphohydrolasePTEN protein, human

Identifiers

PMID28497778
PMCPMC5437297
OpenAlexW2613290483

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.