Evidence map›Paper›PMID 28860594›Full record

ArticleScientific reports2017

SIRT6 promotes osteogenic differentiation of mesenchymal stem cells through BMP signaling.

Ping Zhang, Yunsong Liu, Yuejun Wang, Min Zhang, Longwei Lv, Xiao Zhang, Yongsheng Zhou

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Research advances on silence information regulator 6 as a potential therapeutic target for bone regeneration and repair.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2024
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  16. Inhibitory Effect of Sirtuin6 (SIRT6) on Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells.Medical science monitor : international medical journal of experimental and clinical research · 2019
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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.

Ping ZhangDepartment of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing, 100081, China.
Yunsong LiuDepartment of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing, 100081, China.
Yuejun WangDepartment of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing, 100081, China.
Min ZhangDepartment of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing, 100081, China.
Longwei LvDepartment of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing, 100081, China.
Xiao ZhangDepartment of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing, 100081, China.
Yongsheng ZhouDepartment of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing, 100081, China. kqzhouysh@hsc.pku.edu.cn.
Peking University · CNStomatology Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SIRT6 has been identified as an H3K9 deacetylase and a critical regulator of genome stability, telomere integrity, and metabolic homeostasis. Sirt6-deficient mice displayed dramatic phenotypes including profound lymphopenia, loss of subcutaneous fat, lordokyphosis and low bone marrow density. Here, we report that SIRT6 regulates osteogenic differentiation independent of its deacetylase activity in vitro. Further mechanistic studies showed that SIRT6 involves the cell fate determination by modulating bone morphogenetic protein (BMP) signaling. Unexpectedly, this modulation depends upon P300/CBP-associated factor (PCAF). In addition, we observed impaired SIRT6 expression in bone marrow mesenchymal stem cells and in bone sections of ovariectomized mice. Taken together, our present study provide new insights into mechanisms of SIRT6-regulated MSC function beyond its H3K9 deacetylase activity.

Indexed as

OsteogenesisAnimalsBone Morphogenetic ProteinsCell DifferentiationCells, CulturedFemaleGene Expression RegulationHistone DeacetylasesMesenchymal Stem CellsMiceOvariectomyp300-CBP-Associated Factorp300-CBP Transcription FactorsSignal TransductionSirtuinsBone Morphogenetic ProteinsHistone Deacetylasesp300-CBP-Associated Factorp300-CBP Transcription FactorsSirt6 protein, mouseSirtuins

Identifiers

PMID28860594
PMCPMC5578964
OpenAlexW2745886617

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.