Evidence map›Paper›PMID 25146643›Full record

ArticleJournal of visualized experiments : JoVE2014

Modeling astrocytoma pathogenesis in vitro and in vivo using cortical astrocytes or neural stem cells from conditional, genetically engineered mice.

Robert S McNeill, Ralf S Schmid, Ryan E Bash, Mark Vitucci, Kristen K White, Andrea M Werneke, Brian H Constance, Byron Huff, C Ryan Miller

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

9 authors at 4 institutions in 1 country.

Robert S McNeillDepartment of Pathology and Laboratory Medicine, University of North Carolina School of Medicine.
Ralf S SchmidLineberger Comprehensive Cancer Center, University of North Carolina School of Medicine.
Ryan E BashDivision of Neuropathology, Department of Pathology and Laboratory Medicine, University of North Carolina School of Medicine.
Mark VitucciCurriculum in Genetics and Molecular Biology, University of North Carolina School of Medicine.
Kristen K WhiteDepartment of Pathology and Laboratory Medicine, University of North Carolina School of Medicine.
Andrea M WernekeDivision of Neuropathology, Department of Pathology and Laboratory Medicine, University of North Carolina School of Medicine.
Brian H ConstanceBiological and Biomedical Sciences Program, University of North Carolina School of Medicine.
Byron HuffDepartment of Radiation Oncology, Emory University School of Medicine.
C Ryan MillerLineberger Comprehensive Cancer Center, University of North Carolina School of Medicine; Division of Neuropathology, Department of Pathology and Laboratory Medicine, University of North Carolina School of Medicine; Department of Neurology, Neurosciences Center, University of North Carolina School of Medicine; rmiller@med.unc.edu.
University of North Carolina at Chapel Hill · USCenter for Neurosciences · USEmory University · USUNC Lineberger Comprehensive Cancer Center

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current astrocytoma models are limited in their ability to define the roles of oncogenic mutations in specific brain cell types during disease pathogenesis and their utility for preclinical drug development. In order to design a better model system for these applications, phenotypically wild-type cortical astrocytes and neural stem cells (NSC) from conditional, genetically engineered mice (GEM) that harbor various combinations of floxed oncogenic alleles were harvested and grown in culture. Genetic recombination was induced in vitro using adenoviral Cre-mediated recombination, resulting in expression of mutated oncogenes and deletion of tumor suppressor genes. The phenotypic consequences of these mutations were defined by measuring proliferation, transformation, and drug response in vitro. Orthotopic allograft models, whereby transformed cells are stereotactically injected into the brains of immune-competent, syngeneic littermates, were developed to define the role of oncogenic mutations and cell type on tumorigenesis in vivo. Unlike most established human glioblastoma cell line xenografts, injection of transformed GEM-derived cortical astrocytes into the brains of immune-competent littermates produced astrocytomas, including the most aggressive subtype, glioblastoma, that recapitulated the histopathological hallmarks of human astrocytomas, including diffuse invasion of normal brain parenchyma. Bioluminescence imaging of orthotopic allografts from transformed astrocytes engineered to express luciferase was utilized to monitor in vivo tumor growth over time. Thus, astrocytoma models using astrocytes and NSC harvested from GEM with conditional oncogenic alleles provide an integrated system to study the genetics and cell biology of astrocytoma pathogenesis in vitro and in vivo and may be useful in preclinical drug development for these devastating diseases.

Indexed as

AllelesAnimalsAstrocytesAstrocytomaCell Line, TransformedGenetic EngineeringGlioblastomaHumansMiceMice, Inbred C57BLNeural Stem CellsOncogenes

Identifiers

PMID25146643
PMCPMC4827968
OpenAlexW2059102588

What OpenQuestion holds

Textmetadata
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.