Evidence map›Paper›PMID 26496036›Full record

ArticleOncotarget2015

c-Maf regulates pluripotency genes, proliferation/self-renewal, and lineage commitment in ROS-mediated senescence of human mesenchymal stem cells.

Pei-Min Chen, Chia-Hua Lin, Nan-Ting Li, Yao-Ming Wu, Ming-Tsan Lin, Shih-Chieh Hung, Men-Luh Yen

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 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
2.2field-weighted citation impact, top 12% 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, 36 citations in OpenAlex.

  1. Cellular senescence and aging: molecular mechanisms and convergent pathways.Cellular and molecular life sciences : CMLS · 2026
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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

7 authors at 2 institutions in 1 country.

Pei-Min ChenDepartment of Obstetrics/Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Chia-Hua LinDepartment of Obstetrics/Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Nan-Ting LiDepartment of Obstetrics/Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Yao-Ming WuResearch Center for Developmental Biology and Regenerative Medicine, National Taiwan University, Taipei, Taiwan.
Ming-Tsan LinDepartment of Surgery, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Shih-Chieh HungInstitute of Clinical Medicine, National Yang-Ming University, Taipei, Taiwan.
Men-Luh YenDepartment of Obstetrics/Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan.
National Taiwan University · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) are therapeutically relevant multilineage and immunomodulatory progenitors. Ex vivo expansion of these rare cells is necessary for clinical application and can result in detrimental senescent effects, with mechanisms still largely unknown. We found that vigorous ex vivo expansion of human adipose tissue-derived MSCs (hAMSCs) results in proliferative decline, cell cycle arrest, and altered differentiation capacity. This senescent phenotype was associated with reactive oxygen species (ROS) accumulation, and with increased expression of G1 cell -cycle inhibitors- p15INK4b and p16INK4a - but decreased expression of pluripotency genes-Oct-4, Sox-2, Nanog, and c-Myc-as well as c-Maf a co-factor of MSC lineage-specific transcription factor and sensitive to oxidative stress. These global changes in the transcriptional and functional programs of proliferation, differentiation, and self-renewal were all mediated by ROS-induced suppression of c-Maf, as evidenced by binding of c-Maf to promoter regions of multiple relevant genes in hAMSCs which could be reduced by exogenous ROS. Our findings implicate the strong effects of ROS on multiple stem cell functions with a central role for c-Maf in stem cell senescence.

Indexed as

Cell ProliferationCellular SenescenceGene Expression RegulationHumansMesenchymal Stem CellsPluripotent Stem CellsProto-Oncogene Proteins c-mafReactive Oxygen SpeciesMAF protein, humanProto-Oncogene Proteins c-mafReactive Oxygen Speciesc-MafGerotargethuman adipose tissue-derived MSCs (hAMSCs)lineage commitmentROS-mediated senescenceself-renewal

Identifiers

PMID26496036
PMCPMC4742114
OpenAlexW1865518201

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.