Evidence map›Paper›PMID 27310018›Full record

ArticlePloS one2016

BarTeL, a Genetically Versatile, Bioluminescent and Granule Neuron Precursor-Targeted Mouse Model for Medulloblastoma.

Gregory M Shackleford, Xiang-He Shi, Kimberly S Swanson, Min Y Mahdi, Ignacio Gonzalez-Gomez, Shahab Asgharzadeh, Massimo D'Apuzzo, Anat Erdreich-Epstein, Rex A Moats

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Developmental stage-specific proliferation and retinoblastoma genesis in RB-deficient human but not mouse cone precursors.Proceedings of the National Academy of Sciences of the United States of America · 2018
    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

9 authors at 2 institutions in 1 country.

Gregory M ShacklefordDivision of Hematology, Oncology and Blood & Marrow Transplantation, Department of Pediatrics, The Saban Research Institute, Children's Hospital Los Angeles, and Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.ORCID http://orcid.org/0000-0003-4831-575X
Xiang-He ShiDivision of Hematology, Oncology and Blood & Marrow Transplantation, Department of Pediatrics, The Saban Research Institute, Children's Hospital Los Angeles, and Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
Kimberly S SwansonDivision of Hematology, Oncology and Blood & Marrow Transplantation, Department of Pediatrics, The Saban Research Institute, Children's Hospital Los Angeles, and Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
Min Y MahdiDepartment of Radiology, The Saban Research Institute, Children's Hospital Los Angeles, and Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
Ignacio Gonzalez-GomezDepartment of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
Shahab AsgharzadehDivision of Hematology, Oncology and Blood & Marrow Transplantation, Department of Pediatrics, The Saban Research Institute, Children's Hospital Los Angeles, and Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
Massimo D'ApuzzoDepartment of Pathology, City of Hope National Medical Center, Duarte, California, United States of America.
Anat Erdreich-EpsteinDivision of Hematology, Oncology and Blood & Marrow Transplantation, Department of Pediatrics, The Saban Research Institute, Children's Hospital Los Angeles, and Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
Rex A MoatsDepartment of Radiology, The Saban Research Institute, Children's Hospital Los Angeles, and Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
University of Southern California · USCity Of Hope National Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medulloblastomas are the most common malignant pediatric brain tumor and have been divided into four major molecular subgroups. Animal models that mimic the principal molecular aberrations of these subgroups will be important tools for preclinical studies and allow greater understanding of medulloblastoma biology. We report a new transgenic model of medulloblastoma that possesses a unique combination of desirable characteristics including, among others, the ability to incorporate multiple and variable genes of choice and to produce bioluminescent tumors from a limited number of somatic cells within a normal cellular environment. This model, termed BarTeL, utilizes a Barhl1 homeobox gene promoter to target expression of a bicistronic transgene encoding both the avian retroviral receptor TVA and an eGFP-Luciferase fusion protein to neonatal cerebellar granule neuron precursor (cGNP) cells, which are cells of origin for the sonic hedgehog (SHH) subgroup of human medulloblastomas. The Barhl1 promoter-driven transgene is expressed strongly in mammalian cGNPs and weakly or not at all in mature granule neurons. We efficiently induced bioluminescent medulloblastomas expressing eGFP-luciferase in BarTeL mice by infection of a limited number of somatic cGNPs with avian retroviral vectors encoding the active N-terminal fragment of SHH and a stabilized MYCN mutant. Detection and quantification of the increasing bioluminescence of growing tumors in young BarTeL mice was facilitated by the declining bioluminescence of their uninfected maturing cGNPs. Inclusion of eGFP in the transgene allowed enriched sorting of cGNPs from neonatal cerebella. Use of a single bicistronic avian vector simultaneously expressing both Shh and Mycn oncogenes increased the medulloblastoma incidence and aggressiveness compared to mixed virus infections. Bioluminescent tumors could also be produced by ex vivo transduction of neonatal BarTeL cerebellar cells by avian retroviruses and subsequent implantation into nontransgenic cerebella. Thus, BarTeL mice provide a versatile model with opportunities for use in medulloblastoma biology and therapeutics.

Indexed as

Founder EffectAnimalsAnimals, NewbornAvian ProteinsCell DifferentiationCerebellar NeoplasmsCerebellumDisease Models, AnimalGene Expression Regulation, DevelopmentalGenes, ReporterGenetic VectorsGreen Fluorescent ProteinsHedgehog ProteinsHumansLuciferasesLuminescent MeasurementsAvian ProteinsBarhl1 protein, mouseenhanced green fluorescent proteinGreen Fluorescent ProteinsHedgehog ProteinsLuciferasesMYCN protein, mouseNerve Tissue ProteinsN-Myc Proto-Oncogene ProteinReceptors, VirusRepressor ProteinsShh protein, mouseTva receptor

Identifiers

PMID27310018
PMCPMC4911170
OpenAlexW2440869444

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.