Evidence map›Paper›PMID 23505541›Full record

ArticlePloS one2013

MUC1* ligand, NM23-H1, is a novel growth factor that maintains human stem cells in a more naïve state.

Benoit J Smagghe, Andrew K Stewart, Mark G Carter, Laura M Shelton, Kyle J Bernier, Eric J Hartman, Amy K Calhoun, Vasilios M Hatziioannou, Gabriele Lillacci, Brian A Kirk and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Effective CAR T-cell targeting of an MUC1 cleavage product.Journal for immunotherapy of cancer · 2025
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. The primitive growth factor NME7Biochemistry and biophysics reports · 2019
    Article
  8. Review
  9. The 'known-knowns', and 'known-unknowns' of extracellular Nm23-H1/NDPK proteins.Laboratory investigation; a journal of technical methods and pathology · 2018
    Review
  10. Extracellular NME proteins: a player or a bystander?Laboratory investigation; a journal of technical methods and pathology · 2018
    Review
  11. Review
  12. Induced pluripotent stem cells as a cellular model for studying Down Syndrome.Journal of stem cells & regenerative medicine · 2016
    Review
  13. Review
  14. Review
  15. Review
  16. 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

13 authors at 2 institutions in 1 country.

Benoit J SmaggheMinerva Biotechnologies, Waltham, Massachusetts, United States of America.
Andrew K Stewart
Mark G Carter
Laura M Shelton
Kyle J Bernier
Eric J Hartman
Amy K Calhoun
Vasilios M Hatziioannou
Gabriele Lillacci
Brian A Kirk
Brian A DiNardo
Kenneth S Kosik
Cynthia Bamdad
Minerva Biotechnologies (United States) · USUniversity of California, Santa Barbara · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report that a single growth factor, NM23-H1, enables serial passaging of both human ES and iPS cells in the absence of feeder cells, their conditioned media or bFGF in a fully defined xeno-free media on a novel defined, xeno-free surface. Stem cells cultured in this system show a gene expression pattern indicative of a more "naïve" state than stem cells grown in bFGF-based media. NM23-H1 and MUC1* growth factor receptor cooperate to control stem cell self-replication. By manipulating the multimerization state of NM23-H1, we override the stem cell's inherent programming that turns off pluripotency and trick the cells into continuously replicating as pluripotent stem cells. Dimeric NM23-H1 binds to and dimerizes the extra cellular domain of the MUC1* transmembrane receptor which stimulates growth and promotes pluripotency. Inhibition of the NM23-H1/MUC1* interaction accelerates differentiation and causes a spike in miR-145 expression which signals a cell's exit from pluripotency.

Indexed as

Antibodies, MonoclonalBinding, CompetitiveBiomarkersCell DifferentiationCells, CulturedCulture Media, ConditionedEmbryonic Stem CellsFibroblast Growth Factor 2FibroblastsHumansInduced Pluripotent Stem CellsLigandsMicroRNAsMucin-1NM23 Nucleoside Diphosphate KinasesProtein BindingAntibodies, MonoclonalBiomarkersCulture Media, ConditionedFibroblast Growth Factor 2LigandsMicroRNAsMIRN145 microRNA, humanMucin-1NM23 Nucleoside Diphosphate Kinases

Identifiers

PMID23505541
PMCPMC3591366
OpenAlexW2091817098

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.