Evidence map›Paper›PMID 25254335›Full record

ArticleStem cell reports2014

Enhanced fitness of adult spermatogonial stem cells bearing a paternal age-associated FGFR2 mutation.

Laura A Martin, Nicholas Assif, Moses Gilbert, Dinali Wijewarnasuriya, Marco Seandel

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. Stem cell competition.Current topics in developmental biology · 2026
    Review
  2. Review
  3. Prevalence and genetics of "de novo" MEN2 syndromes.The Journal of clinical endocrinology and metabolism · 2025
    Article
  4. Review
  5. Article
  6. Viral Transduction of Mammalian Spermatogonial Stem Cells.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Spermatogonial stem cells.Biology of reproduction · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Visualizing the origins of selfish de novo mutations in individual seminiferous tubules of human testes.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  20. Genetics of gonadal stem cell renewal.Annual review of cell and developmental biology · 2015
    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

5 authors at 1 institution in 1 country.

Laura A MartinDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
Nicholas AssifDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
Moses GilbertDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
Dinali WijewarnasuriyaDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
Marco SeandelDepartment of Surgery, Weill Cornell Medical College, New York, NY 10065, USA. Electronic address: mseandel@med.cornell.edu.
Cornell University · US

Funding

Clonal competition in stem cells as a driver of paternal age effect diseasesDP2HD080352 · NICHD · WEILL MEDICAL COLL OF CORNELL UNIV · PI SEANDEL, MARCO · 2013 to 2013
$2.5M
NCCDPHP CDC HHS 1DP2HD080352-01NICHD NIH HHS DP2 HD080352
6 · The paper itself

Abstract

Pathogenic de novo mutations increase with fathers' age and could be amplified through competition between genetically distinct subpopulations of spermatogonial stem cells (SSCs). Here, we tested the fitness of SSCs bearing wild-type human FGFR2 or an Apert syndrome mutant, FGFR2 (S252W), to provide experimental evidence for SSC competition. The S252W allele conferred enhanced FGFR2-mediated signaling, particularly at very low concentrations of ligand, and also subtle changes in gene expression. Mutant SSCs exhibited improved competitiveness in vitro and increased stem cell activity in vivo upon transplantation. The fitness advantage in vitro only occurred in low concentrations of fibroblast growth factor (FGF), was independent of FGF-driven proliferation, and was accompanied by increased response to glial cell line-derived neurotrophic factor (GDNF). Our studies provide experimental evidence of enhanced stem cell fitness in SSCs bearing a paternal age-associated mutation. Our model will be useful for interrogating other candidate mutations in the future to reveal mechanisms of disease risk.

Indexed as

AllelesAnimalsCells, CulturedGlial Cell Line-Derived Neurotrophic FactorHumansMaleMiceMice, Inbred C57BLPaternal AgePolymorphism, Single NucleotideReceptor, Fibroblast Growth Factor, Type 2SpermatogoniaStem CellsStem Cell TransplantationTestisGlial Cell Line-Derived Neurotrophic FactorReceptor, Fibroblast Growth Factor, Type 2

Identifiers

PMID25254335
PMCPMC4176532
OpenAlexW2056018961

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.