Evidence map›Paper›PMID 25790378›Full record

ArticlePloS one2015

Biphasic effects of FGF2 on adipogenesis.

Sooho Kim, Chihoon Ahn, Naeun Bong, Senyon Choe, Dong Kun Lee

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Breast Cancer Progression by the FGF/FGFR Axis: A Metabolic Perspective.Journal of mammary gland biology and neoplasia · 2025
    Review
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  14. FGF-2-dependent signaling activated in aged human skeletal muscle promotes intramuscular adipogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2021
    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

5 authors at 1 institution in 1 country.

Sooho KimLaboratory of Genome to Drug Medicine, joint Center for Biosciences, Incheon, Korea.
Chihoon AhnLaboratory of Synthetic Biology, joint Center for Biosciences, Incheon, Korea.
Naeun BongLaboratory of Genome to Drug Medicine, joint Center for Biosciences, Incheon, Korea.
Senyon ChoeLaboratory of Synthetic Biology, joint Center for Biosciences, Incheon, Korea.
Dong Kun LeeLaboratory of Genome to Drug Medicine, joint Center for Biosciences, Incheon, Korea.
Intelligent Synthetic Biology Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although stem cells from mice deficient of FGF2 have been reported to display enhanced capacity for adipogenesis, the literature using in vitro cell culture system has so far reported conflicting results on the role of FGF2 in adipogenesis. We here demonstrate that FGF2, depending on concentration, can function as either a positive or negative factor of in vitro adipogenesis by regulating activation of the ERK signaling pathway. FGF2 at concentrations lower than 2 ng/ml enhanced in vitro adipogenesis of human adipose-derived stem cells (hASCs). However, FGF2 at concentrations higher than 10 ng/ml was able to suppress adipogenesis by maintaining sustained phosphorylation of ERK and function as a dominant negative adipogenic factor toward BMP ligands. Expression levels of FGF2 in the fat tissues from high fat diet induced obese C57BL/6 mice were lower than those from normal chow diet mice, indicating that expression levels of FGF2 in the fat tissues might be in reverse correlation with the size of fat tissues. Our observation of concentration dependent biphasic effect as well as dominant negative effect of FGF2 on adipogenesis provides a mechanistic basis to understand roles of FGF2 in adipogenesis and development of fat tissues.

Indexed as

AdipogenesisAdipocytesAdipose TissueAnimalsCell DifferentiationCells, CulturedDiet, High-FatDisease Models, AnimalFibroblast Growth Factor 2HumansMaleMAP Kinase Signaling SystemMesenchymal Stem CellsMiceMice, Inbred C57BLObesityFibroblast Growth Factor 2

Identifiers

PMID25790378
PMCPMC4366188
OpenAlexW2088522347

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.