Evidence map›Paper›PMID 25794107›Full record

ArticlePloS one2015

Pancreatic endoplasmic reticulum kinase activation promotes medulloblastoma cell migration and invasion through induction of vascular endothelial growth factor A.

Stephanie Jamison, Yifeng Lin, Wensheng Lin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Targeting Angiogenic Factors for the Treatment of Medulloblastoma.Current treatment options in oncology · 2022
    Review
  6. Review
  7. Review
  8. Article
  9. Perillyl alcohol for pediatric TP53- and RAS-mutated SHH-medulloblastoma: an in vitro and in vivo translational pre-clinical study.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Frontiers in microbiology · 2018
    Review
  17. Article
  18. Article
  19. Article
  20. Article
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

3 authors at 1 institution in 1 country.

Stephanie JamisonDepartment of Neuroscience, University of Minnesota, Minneapolis, United States of America; Institute for Translational Neuroscience, University of Minnesota, Minneapolis, United States of America; Masonic Cancer Center, University of Minnesota, Minneapolis, United States of America.
Yifeng LinDepartment of Neuroscience, University of Minnesota, Minneapolis, United States of America; Institute for Translational Neuroscience, University of Minnesota, Minneapolis, United States of America; Masonic Cancer Center, University of Minnesota, Minneapolis, United States of America.
Wensheng LinDepartment of Neuroscience, University of Minnesota, Minneapolis, United States of America; Institute for Translational Neuroscience, University of Minnesota, Minneapolis, United States of America; Masonic Cancer Center, University of Minnesota, Minneapolis, United States of America.
University of Minnesota · US

Funding

The effects of the unfolded protein response on medulloblastomaR01NS073132 · NINDS · UNIVERSITY OF SOUTH ALABAMA · PI LIN, WENSHENG · 2011 to 2015
$1.6M
NINDS NIH HHS NS073132NINDS NIH HHS R01 NS073132
6 · The paper itself

Abstract

Evidence is accumulating that activation of the pancreatic endoplasmic reticulum kinase (PERK) in response to endoplasmic reticulum (ER) stress adapts tumor cells to the tumor microenvironment and enhances tumor angiogenesis by inducing vascular endothelial growth factor A (VEGF-A). Recent studies suggest that VEGF-A can act directly on certain tumor cell types in an autocrine manner, via binding to VEGF receptor 2 (VEGFR2), to promote tumor cell migration and invasion. Although several reports show that PERK activation increases VEGF-A expression in medulloblastoma, the most common solid malignancy of childhood, the role that either PERK or VEGF-A plays in medulloblastoma remains elusive. In this study, we mimicked the moderate enhancement of PERK activity observed in tumor patients using a genetic approach and a pharmacologic approach, and found that moderate activation of PERK signaling facilitated medulloblastoma cell migration and invasion and increased the production of VEGF-A. Moreover, using the VEGFR2 inhibitor SU5416 and the VEGF-A neutralizing antibody to block VEGF-A/VEGFR2 signaling, our results suggested that tumor cell-derived VEGF-A promoted medulloblastoma cell migration and invasion through VEGFR2 signaling, and that both VEGF-A and VEGFR2 were required for the promoting effects of PERK activation on medulloblastoma cell migration and invasion. Thus, these findings suggest that moderate PERK activation promotes medulloblastoma cell migration and invasion through enhancement of VEGF-A/VEGFR2 signaling.

Indexed as

AdenineCell Line, TumorCell MovementCerebellar NeoplasmseIF-2 KinaseEndoplasmic ReticulumEnzyme ActivationHumansIndolesMedulloblastomaProtein Kinase InhibitorsSignal TransductionVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-27-methyl-5-(1-((3-(trifluoromethyl)phenyl)acetyl)-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo(2,3-d)pyrimidin-4-amineAdenineEIF2AK3 protein, humaneIF-2 KinaseIndolesProtein Kinase InhibitorsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID25794107
PMCPMC4368580
OpenAlexW2084517914

What OpenQuestion holds

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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.