Evidence map›Paper›PMID 18988710›Full record

ArticleStem cells (Dayton, Ohio)2009

Gliotypic neural stem cells transiently adopt tumorigenic properties during normal differentiation.

Noah M Walton, Gregory E Snyder, Donghyun Park, Firas Kobeissy, Bjorn Scheffler, Dennis A Steindler

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
  6. Review
  7. Article
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  9. Article
  10. Stem cell pathologies and neurological disease.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2012
    Review
  11. Article
  12. Article
  13. 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

6 authors at 3 institutions in 2 countries.

Noah M WaltonDepartment of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, Florida 32610, USA.
Gregory E Snyder
Donghyun Park
Firas Kobeissy
Bjorn Scheffler
Dennis A Steindler
University of Florida · USUniversity of Chicago · USLife & Brain (Germany) · DE

Funding

Training In Rehabilitation and Neuromuscular PlasticityT32HD043730 · NICHD · UNIVERSITY OF FLORIDA · PI DAVID D FULLER · 2003 to 2026
$5.3M
STUDIES OF ADULT BRAIN NEUROPOIESISR01NS037556 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI STEINDLER, DENNIS A. · 1999 to 2006
$2.6M
STEM/PROGENITOR CELL PROTECTION FOR PARKINSON'S DISEASER01NS055165 · NINDS · UNIVERSITY OF FLORIDA · PI STEINDLER, DENNIS A. · 2007 to 2011
$1.6M
Altering Fate of Hematopoietic and Neural Stem CellsR01HL070143 · NHLBI · UNIVERSITY OF FLORIDA · PI STEINDLER, DENNIS A. · 2003 to 2006
$1.3M
Stem Cell Integration in the Injured HippocampusR21NS046384 · NINDS · UNIVERSITY OF FLORIDA · PI SCHEFFLER, BJORN · 2004 to 2005
$336k
NHLBI NIH HHS HL70143NHLBI NIH HHS R01 HL070143NICHD NIH HHS T32 HD043730NICHD NIH HHS T32HD043730NINDS NIH HHS NS055165NINDS NIH HHS NS37556NINDS NIH HHS NS46384NINDS NIH HHS R01 NS037556NINDS NIH HHS R01 NS055165NINDS NIH HHS R21 NS046384
6 · The paper itself

Abstract

An increasing body of evidence suggests that astrocytic gliomas of the central nervous system may be derived from gliotypic neural stem cells. To date, the study of these tumors, particularly the identification of originating cellular population(s), has been frustrated by technical difficulties in accessing the native niche of stem cells. To identify any hallmark signs of cancer in neural stem cells or their progeny, we cultured subventricular zone-derived tissue in a unique in vitro model that temporally and phenotypically recapitulates adult neurogenesis. Contrary to some reports, we found undifferentiated neural stem cells possess few characteristics, suggesting prototumorigenic potential. However, when induced to differentiate, neural stem cells give rise to intermediate progenitors that transiently exhibit multiple glioma characteristics, including aneuploidy, loss of growth-contact inhibition, alterations in cell cycle, and growth factor insensitivity. Further examination of progenitor populations revealed a subset of cells defined by the aberrant expression of (the pathological glioma marker) class III beta-tubulin that exhibit intrinsic parental properties of gliomas, including multilineage differentiation and continued proliferation in the absence of a complex cellular regulatory environment. As tumorigenic characteristics in progenitor cells normally disappear with the generation of mature progeny, this suggests that developmentally intermediate progenitor cells, rather than neural stem cells, may be the origin of so-called "stem cell-derived" tumors.

Indexed as

AnimalsAstrocytesBiomarkers, TumorBlotting, WesternCell DifferentiationCells, CulturedFlow CytometryGliomaImmunohistochemistryMiceMice, Inbred C57BLMicroscopy, Electron, TransmissionNeuronsPolymerase Chain ReactionStem CellsTubulinBiomarkers, TumorTubulin

Identifiers

PMID18988710
PMCPMC4425277
OpenAlexW2036709952

What OpenQuestion holds

Textmetadata
LicenceTDM
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.