Evidence map›Paper›PMID 23861869›Full record

ArticlePloS one2013

Cytomegalovirus pp71 protein is expressed in human glioblastoma and promotes pro-angiogenic signaling by activation of stem cell factor.

Lisa A Matlaf, Lualhati E Harkins, Vladimir Bezrookove, Charles S Cobbs, Liliana Soroceanu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Cytomegalovirus DNA in non-glioblastoma multiforme brain tumors of infants.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Article
  10. Review
  11. Review
  12. Expanding the Known Functional Repertoire of the Human Cytomegalovirus pp71 Protein.Frontiers in cellular and infection microbiology · 2020
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Novel drugs in pediatric gliomas.Oncology letters · 2017
    Article
  18. Article
  19. Evaluation of JC and Cytomegalo Viruses in Glioblastoma TissueAsian Pacific journal of cancer prevention : APJCP · 2016
    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

5 authors at 1 institution in 1 country.

Lisa A MatlafCalifornia Pacific Medical Center Research Institute, San Francisco, California, USA.
Lualhati E Harkins
Vladimir Bezrookove
Charles S Cobbs
Liliana Soroceanu
California Pacific Medical Center · US

Funding

Cytomegalovirus Gene Expression and Strain Variability in Glioma PathogenesisR01NS070289 · NINDS · SWEDISH MEDICAL CENTER, FIRST HILL · PI COBBS, CHARLES S · 2010 to 2014
$1.9M
Modulation of Glioma Growth and Invasion by HCMV Glycoprotein BR21NS067395 · NINDS · CALIFORNIA PACIFIC MED CTR RES INSTITUTE · PI SOROCEANU, LILIANA · 2009 to 2010
$462k
NINDS NIH HHS 1R21NS067395-01NINDS NIH HHS R01 NS070289NINDS NIH HHS R01NS070289-02NINDS NIH HHS R21 NS067395
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is a highly malignant primary central nervous system neoplasm characterized by tumor cell invasion, robust angiogenesis, and a mean survival of 15 months. Human cytomegalovirus (HCMV) infection is present in >90% of GBMs, although the role the virus plays in GBM pathogenesis is unclear. We report here that HCMV pp71, a viral protein previously shown to promote cell cycle progression, is present in a majority of human GBMs and is preferentially expressed in the CD133+, cancer stem-like cell population. Overexpression of pp71 in adult neural precursor cells resulted in potent induction of stem cell factor (SCF), an important pro-angiogenic factor in GBM. Using double immunofluorescence, we demonstrate in situ co-localization of pp71 and SCF in clinical GBM specimens. pp71 overexpression in both normal and transformed glial cells increased SCF secretion and this effect was specific, since siRNA mediated knockdown of pp71 or treatment with the antiviral drug cidofovir resulted in decreased expression and secretion of SCF by HCMV-infected cells. pp71- induced upregulation of SCF resulted in downstream activation of its putative endothelial cell receptor, c-kit, and angiogenesis as measured by increased capillary tube formation in vitro. We demonstrate that pp71 induces a pro-inflammatory response via activation of NFΚB signaling which drives SCF expression. Furthermore, we show that pp71 levels and NFKB activation are selectively augmented in the mesenchymal subtype of human GBMs, characterized by worst patient outcome, suggesting that HCMV pp71-induced paracrine signaling may contribute to the aggressive phenotype of this human malignancy.

Indexed as

Signal TransductionCell Line, TumorCytomegalovirusGene ExpressionGene Expression ProfilingGlioblastomaHumansHuman Umbilical Vein Endothelial CellsNeovascularization, PathologicNF-kappa BStem Cell FactorViral Proteinscytomegalovirus phosphoprotein 71kDaNF-kappa BStem Cell FactorViral Proteins

Identifiers

PMID23861869
PMCPMC3702580
OpenAlexW2020723426

What OpenQuestion holds

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Registered trials

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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.