Evidence map›Paper›PMID 20739545›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

Impaired orthotopic glioma growth and vascularization in transgenic mouse models of Alzheimer's disease.

Daniel Paris, Nowel Ganey, Magdalena Banasiak, Vincent Laporte, Nikunj Patel, Myles Mullan, Susan F Murphy, Gi-Taek Yee, Corbin Bachmeier, Christopher Ganey and 4 more

Abstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. 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
–field-weighted citation impact
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.

  1. Accumulation of amyloid beta in human glioblastomas.Clinical and experimental immunology · 2020
    Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Accumulation of Innate Amyloid Beta Peptide in Glioblastoma Tumors.International journal of molecular sciences · 2019
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Human apolipoprotein E ɛ4 expression impairs cerebral vascularization and blood-brain barrier function in mice.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2015
    Article
  16. Article
  17. Article
  18. Brain microvasculature and hypoxia-related proteins in Alzheimer's disease.International journal of clinical and experimental pathology · 2011
    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

14 authors.

Daniel ParisThe Roskamp Institute, Sarasota, Florida 34243, USA. dparis@rfdn.org
Nowel Ganey
Magdalena Banasiak
Vincent Laporte
Nikunj Patel
Myles Mullan
Susan F Murphy
Gi-Taek Yee
Corbin Bachmeier
Christopher Ganey
David Beaulieu-Abdelahad
Venkatarajan S Mathura
Steven Brem
Michael Mullan

Funding

Amyloid peptides and angiogenesisR01AG019250 · NIA · UNIVERSITY OF SOUTH FLORIDA · PI MULLAN, MICHAEL J · 2001 to 2009
$2.3M
NIA NIH HHS R01 AG019250PHS HHS R01A619250
6 · The paper itself

Abstract

Alzheimer's disease (AD) is the most common form of dementia among the aging population and is characterized pathologically by the progressive intracerebral accumulation of beta-amyloid (Abeta) peptides and neurofibrillary tangles. The level of proangiogenic growth factors and inflammatory mediators with proangiogenic activity is known to be elevated in AD brains which has led to the supposition that the cerebrovasculature of AD patients is in a proangiogenic state. However, angiogenesis depends on the balance between proangiogenic and antiangiogenic factors and the brains of AD patients also show an accumulation of endostatin and Abeta peptides which have been shown to be antiangiogenic. To determine whether angiogenesis is compromised in the brains of two transgenic mouse models of AD overproducing Abeta peptides (Tg APPsw and Tg PS1/APPsw mice), we assessed the growth and vascularization of orthotopically implanted murine gliomas since they require a high degree of angiogenesis to sustain their growth. Our data reveal that intracranial tumor growth and angiogenesis is significantly reduced in Tg APPsw and Tg PS1/APPsw mice compared with their wild-type littermates. In addition, we show that Abeta inhibits the angiogenesis stimulated by glioma cells when cocultured with human brain microvascular cells on a Matrigel layer. Altogether our data suggest that the brain of transgenic mouse models of AD does not constitute a favorable environment to support neoangiogenesis and may explain why vascular insults synergistically precipitate the cognitive presentation of AD.

Indexed as

Alzheimer DiseaseAnimalsBrain NeoplasmsCell Line, TumorCells, CulturedCoculture TechniquesCricetinaeDisease Models, AnimalGliomaHumansMiceMice, TransgenicNeoplasm TransplantationNeovascularization, Pathologic

Identifiers

PMID20739545
PMCPMC2935547

What OpenQuestion holds

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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.