Evidence map›Paper›PMID 21881602›Full record

ArticleCell death & disease2011

Distribution of CD133 reveals glioma stem cells self-renew through symmetric and asymmetric cell divisions.

J D Lathia, M Hitomi, J Gallagher, S P Gadani, J Adkins, A Vasanji, L Liu, C E Eyler, J M Heddleston, Q Wu and 11 more

Abstract read
In one paragraph

Article in Cell death & disease, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers.

0numbers the graph read from it
0cells of the map it votes in
110citing 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

110 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Frontiers in cell and developmental biology · 2026
    Review
  6. Frontiers in cell and developmental biology · 2026
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Glioma Stem Cells: Novel Data Obtained by Single-Cell Sequencing.International journal of molecular sciences · 2022
    Review
  17. Review
  18. Review
  19. Article
  20. Article

50 more citing papers are in PubMed but not listed here.

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

21 authors.

J D LathiaDepartment of Stem Cell Biology and Regenerative Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA. lathiaj@ccf.org
M Hitomi
J Gallagher
S P Gadani
J Adkins
A Vasanji
L Liu
C E Eyler
J M Heddleston
Q Wu
S Minhas
A Soeda
D J Hoeppner
R Ravin
R D G McKay
R E McLendon
D Corbeil
A Chenn
A B Hjelmeland
D M Park
J N Rich

Funding

Stem Cell Biology And Brain DiseaseZIANS002981 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI MCKAY, RONALD · 2009 to 2011
$6.6M
Targeting Brain Tumor Stem Cells Through Novel Therapeutic CombinationsR01CA154130 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI RICH, JEREMY N · 2010 to 2014
$1.9M
Stem Cell-Like Glioma Cells in AngiogenesisR01CA129958 · NCI · DUKE UNIVERSITY · PI RICH, JEREMY N · 2008 to 2012
$1.6M
TGFbeta-PTEN Interactions in Glioma Biology & TherapyR01CA116659 · NCI · DUKE UNIVERSITY · PI RICH, JEREMY N · 2006 to 2010
$1.4M
A20 Promotes Glioma Stem Cell Mediated TumorigenesisR01CA151522 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HJELMELAND, ANITA BORTON · 2010 to 2014
$1.2M
Molecular Mechanisms of SPARC Mediated Glioma InvasionR01NS054276 · NINDS · DUKE UNIVERSITY · PI RICH, JEREMY N · 2006 to 2010
$1.2M
ATM (Ataxia Telangiectasia Mutated) signaling through cyclin D1R21NS063057 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI HITOMI, MASAHIRO · 2010 to 2011
$428k
Integrin regulation of brain tumor initiating cellsF32CA142159 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI LATHIA, JUSTIN D. · 2009 to 2011
$98k
Targeting Brain Tumor Stem CellsF30NS063496 · NINDS · DUKE UNIVERSITY · PI EYLER, CHRISTINE ELISSA · 2009 to 2010
$61k
NCI NIH HHS CA116659NCI NIH HHS CA129958NCI NIH HHS CA151522NCI NIH HHS CA154130NCI NIH HHS F32 CA142159NCI NIH HHS R01 CA116659NCI NIH HHS R01 CA129958NCI NIH HHS R01 CA151522NCI NIH HHS R01 CA154130NINDS NIH HHS F30 NS063496NINDS NIH HHS NS054276NINDS NIH HHS R01 NS054276NINDS NIH HHS R21 NS063057
6 · The paper itself

Abstract

Malignant gliomas contain a population of self-renewing tumorigenic stem-like cells; however, it remains unclear how these glioma stem cells (GSCs) self-renew or generate cellular diversity at the single-cell level. Asymmetric cell division is a proposed mechanism to maintain cancer stem cells, yet the modes of cell division that GSCs utilize remain undetermined. Here, we used single-cell analyses to evaluate the cell division behavior of GSCs. Lineage-tracing analysis revealed that the majority of GSCs were generated through expansive symmetric cell division and not through asymmetric cell division. The majority of differentiated progeny was generated through symmetric pro-commitment divisions under expansion conditions and in the absence of growth factors, occurred mainly through asymmetric cell divisions. Mitotic pair analysis detected asymmetric CD133 segregation and not any other GSC marker in a fraction of mitoses, some of which were associated with Numb asymmetry. Under growth factor withdrawal conditions, the proportion of asymmetric CD133 divisions increased, congruent with the increase in asymmetric cell divisions observed in the lineage-tracing studies. Using single-cell-based observation, we provide definitive evidence that GSCs are capable of different modes of cell division and that the generation of cellular diversity occurs mainly through symmetric cell division, not through asymmetric cell division.

Indexed as

AC133 AntigenAntigens, CDCell DivisionCell LineageEpidermal Growth FactorFibroblast Growth Factor 2GliomaGlycoproteinsHumansLamininMitosisNeoplastic Stem CellsPeptidesAC133 AntigenAntigens, CDEpidermal Growth FactorFibroblast Growth Factor 2GlycoproteinsLamininPeptidesPROM1 protein, human

Identifiers

PMID21881602
PMCPMC3186899

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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.