Evidence map›Paper›PMID 27530621›Full record

ArticleIn vitro cellular & developmental biology. Animal2016

SIRT1 was involved in TNF-α-promoted osteogenic differentiation of human DPSCs through Wnt/β-catenin signal.

Guijuan Feng, Ke Zheng, Donghui Song, Ke Xu, Dan Huang, Ye Zhang, Peipei Cao, Shuling Shen, Jinlong Zhang, Xingmei Feng and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 49 citations in OpenAlex.

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  13. SIRT1 Gene SNP rs932658 Is Associated With Medication-Related Osteonecrosis of the Jaw.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2021
    Article
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  15. Review
  16. Polyphenols in Dental Applications.Bioengineering (Basel, Switzerland) · 2020
    Review
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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

11 authors at 3 institutions in 1 country.

Guijuan FengDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Ke ZhengDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Donghui SongDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Ke XuDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Dan HuangDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Ye ZhangDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Peipei CaoDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Shuling ShenDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Jinlong ZhangDepartment of Spine Surgery, The Second Affiliated Hospital of Nantong University, Nantong, 226001, China.
Xingmei FengDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China. fengxingmeint@126.com.
Dongmei ZhangDepartment of Pathogen Biology, Medical College, Nantong University, Nantong, 226001, China. zdm060808@aliyun.com.
Nantong University · CNAffiliated Hospital of Nantong University · CNSecond Affiliated Hospital of Nantong University

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dental pulp stem cells (DPSCs), as one type of mesenchymal stem cells (MSCs), have the capability of self-renewal and differentiating along the various directions, including osteogenic, chondrogenic, neurogenic, and adipogenic. We previously study and found that tumor necrosis factor-α (TNF-α) promoted osteogenic differentiation of human DPSCs via the Wnt/β-catenin signaling pathway in low concentration while inhibited that in high concentration. In the abovementioned process, we found that sirtuin-1 (SIRT1) had the same change compared with the characteristic protein of bone formation, such as bone morphogenetic protein 2 (BMP2), runt-related transcription factor 2 (Runx2), and collagen I (COL1). We asked whether SIRT1 could regulate osteogenesis of DPSCs. In inflammation microenvironment constructed by TNF-α, we tested the expression changing of SIRT1 and analyzed the function of SIRT1 on osteogenic differentiation of DPSCs. SIRT1 deacetylated β-catenin, and then promote its accumulation in the nucleus. Accumulated β-catenin can lead to transcription of osteogenic characteristic genes. Using the activator of SIRT1, resveratrol, could promote the above-mentioned process of osteogenic differentiation. SIRT1 could regulate osteogenesis of DPSCs through Wnt/β-catenin signal. SIRT1, as a regulator of differentiation of DPSCs, may be a new target for cell-based therapy in oral diseases and other regenerative medicine.

Indexed as

AcetylationAdolescentAdultbeta CateninCell DifferentiationDental PulpHumansOsteogenesisSirtuin 1Stem CellsTumor Necrosis Factor-alphaWnt Signaling PathwayYoung Adultbeta CateninSirtuin 1Tumor Necrosis Factor-alphaDPSCsOsteogenic differentiationSIRT1Wnt/β-catenin

Identifiers

PMID27530621
OpenAlexW2513208783

What OpenQuestion holds

Textmetadata
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.