Evidence map›Paper›PMID 36187229›Full record

ReviewStem cells international2022

Epigenetic Regulation of Methylation in Determining the Fate of Dental Mesenchymal Stem Cells.

Hui Zhang, Hong Fu, Hongzhi Fang, Qing Deng, Hao Huang, Dingyu Hou, Miaomiao Wang, Quanzhou Yao, Qiqi Si, Rui Chen and 4 more

Abstract readReview
In one paragraph

Review in Stem cells international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
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

14 authors.

Hui ZhangCollege of Medicine, Southwest Jiaotong University, Chengdu, Sichuan, China 610031.ORCID https://orcid.org/0000-0002-6905-3181
Hong FuCollege of Medicine, Southwest Jiaotong University, Chengdu, Sichuan, China 610031.ORCID https://orcid.org/0000-0002-7337-4658
Hongzhi FangDepartment of stomatology, The Third People's Hospital of Chengdu, The Affiliated Hospital of Southwest Jiaotong University, Chengdu, Sichuan, China 610000.ORCID https://orcid.org/0000-0002-1270-756X
Qing DengCollege of Medicine, Southwest Jiaotong University, Chengdu, Sichuan, China 610031.ORCID https://orcid.org/0000-0002-7531-9142
Hao HuangCollege of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, Sichuan, China 610031.
Dingyu HouCollege of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, Sichuan, China 610031.
Miaomiao WangCollege of Analysis and Testing Center, Southwest Jiaotong University, Chengdu, Sichuan, China 610031.
Quanzhou YaoCollege of Medicine, Southwest Jiaotong University, Chengdu, Sichuan, China 610031.
Qiqi SiCollege of Life Science, Southwest Jiaotong University, Chengdu, Sichuan, China 610031.ORCID https://orcid.org/0000-0001-8125-0666
Rui ChenCollege of Medicine, Southwest Jiaotong University, Chengdu, Sichuan, China 610031.ORCID https://orcid.org/0000-0003-0257-4385
Linke LiCollege of Medicine, Southwest Jiaotong University, Chengdu, Sichuan, China 610031.ORCID https://orcid.org/0000-0001-7591-7495
Jie WengCollege of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, Sichuan, China 610031.ORCID https://orcid.org/0000-0002-7034-3215
Tailin GuoCollege of Medicine, Southwest Jiaotong University, Chengdu, Sichuan, China 610031.ORCID https://orcid.org/0000-0001-8127-6719
Mengyuan WangDepartment of stomatology, The Third People's Hospital of Chengdu, The Affiliated Hospital of Southwest Jiaotong University, Chengdu, Sichuan, China 610000.ORCID https://orcid.org/0000-0001-9869-6883

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dental mesenchymal stem cells (DMSCs) are crucial in tooth development and periodontal health, and their multipotential differentiation and self-renewal ability play a critical role in tissue engineering and regenerative medicine. Methylation modifications could promote the appropriate biological behavior by postsynthetic modification of DNA or protein and make the organism adapt to developmental and environmental prompts by regulating gene expression without changing the DNA sequence. Methylation modifications involved in DMSC fate include DNA methylation, RNA methylation, and histone modifications, which have been proven to exert a significant effect on the regulation of the fate of DMSCs, such as proliferation, self-renewal, and differentiation potential. Understanding the regulation of methylation modifications on the behavior and the immunoinflammatory responses involved in DMSCs contributes to further study of the mechanism of methylation on tissue regeneration and inflammation. In this review, we briefly summarize the key functions of histone methylation, RNA methylation, and DNA methylation in the differentiation potential and self-renewal of DMSCs as well as the opportunities and challenges for their application in tissue regeneration and disease therapy.

Identifiers

PMID36187229
PMCPMC9522499

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Registered trials

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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.