Evidence map›Paper›PMID 20681019›Full record

ArticleStem cells (Dayton, Ohio)2010

Fibroblast growth factor type 2 signaling is critical for DNA repair in human keratinocyte stem cells.

Ghida Harfouche, Pierre Vaigot, Walid Rachidi, Odile Rigaud, Sandra Moratille, Mélanie Marie, Gilles Lemaitre, Nicolas O Fortunel, Michèle T Martin

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 36 citations in OpenAlex.

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  7. α6 Integrin (α6International journal of molecular sciences · 2017
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  13. Development and homeostasis of the skin epidermis.Cold Spring Harbor perspectives in biology · 2012
    Article
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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 3 institutions in 1 country.

Ghida HarfoucheCEA, iRCM, Laboratory of Genomics and Radiobiology of Keratinopoiesis, Evry, France.
Pierre Vaigot
Walid Rachidi
Odile Rigaud
Sandra Moratille
Mélanie Marie
Gilles Lemaitre
Nicolas O Fortunel
Michèle T Martin
Institut de Radiobiologie Cellulaire et Moléculaire · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRInstitut Nanosciences et Cryogénie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tissue stem cells must be endowed with superior maintenance and repair systems to ensure genomic stability over multiple generations, which would be less necessary in more differentiated cells. We previously reported that human keratinocyte stem cells were more resistant to ionizing radiation toxicity than their direct progeny, the keratinocyte progenitor cells. In the present study we addressed the mechanisms underlying this difference. Investigations of DNA repair showed that both single and double DNA strand breaks were repaired more rapidly and more efficiently in stem cells than in progenitors. As cell signaling is a key regulatory step in the management of DNA damage, a gene profiling study was performed. Data revealed that several genes of the fibroblast growth factor type 2 (FGF2) signaling pathway were induced by DNA damage in stem cells and not in progenitors. Furthermore, an increased content of the FGF2 protein was found in irradiated stem cells, both for the secreted and the cellular forms of the protein. To examine the role of endogenous FGF2 in DNA repair, stem cells were exposed to FGF2 pathway inhibitors. Blocking the FGF2 receptor (FGF receptor 1) or the kinase (Ras-mitogen-activated protein kinase 1) resulted in a inhibition of single and double DNA strand-break repair in the keratinocyte stem cells. Moreover, supplementing the progenitor cells with exogenous FGF2 activated their DNA repair. We propose that, apart from its well-known role as a strong mitogen and prosurvival factor, FGF2 helps to maintain genomic integrity in stem cells by activating stress-induced DNA repair.

Indexed as

DNA Breaks, Double-StrandedDNA Breaks, Single-StrandedDNA RepairSignal TransductionAntibodies, MonoclonalButadienesCell CycleCells, CulturedChromatin Assembly and DisassemblyComet AssayFibroblast Growth Factor 2Gene Expression ProfilingGene Regulatory NetworksGenomic InstabilityHistonesHumansAntibodies, MonoclonalButadienesFibroblast Growth Factor 2H2AX protein, humanHistonesNitrilesProtein Kinase InhibitorsRecombinant ProteinsSerineU 0126

Identifiers

PMID20681019
PMCPMC2996082
OpenAlexW2095051785

What OpenQuestion holds

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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.