Evidence map›Paper›PMID 29284798›Full record

ArticleOncogenesis2017

High expression of MKP1/DUSP1 counteracts glioma stem cell activity and mediates HDAC inhibitor response.

Olatz Arrizabalaga, Leire Moreno-Cugnon, Jaione Auzmendi-Iriarte, Paula Aldaz, Inmaculada Ibanez de Caceres, Laura Garros-Regulez, Veronica Moncho-Amor, Sergio Torres-Bayona, Olga Pernía, Laura Pintado-Berninches and 14 more

Open access · goldAbstract read
In one paragraph

Article in Oncogenesis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Cancers · 2021
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Dual-Specificity Phosphatase Regulation in Neurons and Glial Cells.International journal of molecular sciences · 2019
    Review
  20. Primary cilium and glioblastoma.Therapeutic advances in medical oncology · 2018
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors at 8 institutions in 3 countries.

Olatz ArrizabalagaCellular oncology group, Biodonostia Health Research Institute, San Sebastian, Spain.
Leire Moreno-CugnonCellular oncology group, Biodonostia Health Research Institute, San Sebastian, Spain.
Jaione Auzmendi-IriarteCellular oncology group, Biodonostia Health Research Institute, San Sebastian, Spain.
Paula AldazCellular oncology group, Biodonostia Health Research Institute, San Sebastian, Spain.
Inmaculada Ibanez de CaceresCancer Epigenetics Laboratory, INGEMM, IDIPAZ, Hospital La Paz, Madrid, Spain.
Laura Garros-RegulezCellular oncology group, Biodonostia Health Research Institute, San Sebastian, Spain.
Veronica Moncho-AmorThe Francis Crick Institute, London, UK.
Sergio Torres-BayonaDonostia Hospital, San Sebastian, Spain.
Olga PerníaCancer Epigenetics Laboratory, INGEMM, IDIPAZ, Hospital La Paz, Madrid, Spain.
Laura Pintado-BerninchesInstituto de Investigaciones Biomédicas CSIC/UAM, 28029, Madrid, Spain.
Patricia Carrasco-RamirezInstituto de Investigaciones Biomédicas CSIC/UAM, 28029, Madrid, Spain.
María Cortes-SempereInstituto de Investigaciones Biomédicas CSIC/UAM, 28029, Madrid, Spain.
Rocío RosasCancer Epigenetics Laboratory, INGEMM, IDIPAZ, Hospital La Paz, Madrid, Spain.
Pilar Sanchez-GomezNeuro-Oncology Unit, Instituto de Salud Carlos III-UFIEC, Madrid, Spain.
Irune RuizCellular oncology group, Biodonostia Health Research Institute, San Sebastian, Spain.
Helena CarenDepartment of Pathology, Sahlgrenska Cancer Center, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Steven PollardMRC Centre for Regenerative Medicine, Edinburgh, UK.
Idoia GarciaCellular oncology group, Biodonostia Health Research Institute, San Sebastian, Spain.
Angel-Ayuso SacidoCentro Integral Oncológico Clara Campal (CIOCC) and Instituto de Medicina Molecular Aplicada (IMMA), Madrid, Spain.
Robin Lovell-BadgeThe Francis Crick Institute, London, UK.ORCID http://orcid.org/0000-0001-9364-4179
Cristobal Belda-IniestaCentro Integral Oncológico Clara Campal (CIOCC) and Instituto de Medicina Molecular Aplicada (IMMA), Madrid, Spain.
Nicolas SampronCellular oncology group, Biodonostia Health Research Institute, San Sebastian, Spain.
Rosario PeronaInstituto de Investigaciones Biomédicas CSIC/UAM, 28029, Madrid, Spain. rperona@iib.uam.es.
Ander MatheuCellular oncology group, Biodonostia Health Research Institute, San Sebastian, Spain. ander.matheu@biodonostia.org.
Biogipuzkoa Health Research Institute · ESInstituto de Investigaciones Biomédicas Sols-Morreale · ESHospital La Paz Institute for Health Research · ESIkerbasque · ESThe Francis Crick Institute · GBInstituto de Salud Carlos III · ESMRC Centre for Regenerative Medicine · GBUniversity of Gothenburg · SE

Funding

Medical Research Council MC_U117562207Worldwide Cancer Research 13-1270
6 · The paper itself

Abstract

The elucidation of mechanisms involved in resistance to therapies is essential to improve the survival of patients with malignant gliomas. A major feature possessed by glioma cells that may aid their ability to survive therapy and reconstitute tumors is the capacity for self-renewal. We show here that glioma stem cells (GSCs) express low levels of MKP1, a dual-specificity phosphatase, which acts as a negative inhibitor of JNK, ERK1/2, and p38 MAPK, while induction of high levels of MKP1 expression are associated with differentiation of GSC. Notably, we find that high levels of MKP1 correlate with a subset of glioblastoma patients with better prognosis and overall increased survival. Gain of expression studies demonstrated that elevated MKP1 impairs self-renewal and induces differentiation of GSCs while reducing tumorigenesis in vivo. Moreover, we identified that MKP1 is epigenetically regulated and that it mediates the anti-tumor activity of histone deacetylase inhibitors (HDACIs) alone or in combination with temozolomide. In summary, this study identifies MKP1 as a key modulator of the interplay between GSC self-renewal and differentiation and provides evidence that the activation of MKP1, through epigenetic regulation, might be a novel therapeutic strategy to overcome therapy resistance in glioblastoma.

Identifiers

PMID29284798
PMCPMC5865544
OpenAlexW2773703040

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.