Evidence map›Paper›PMID 35578312›Full record

ReviewStem cell research & therapy2022

Epigenetic therapy targeting bone marrow mesenchymal stem cells for age-related bone diseases.

Yi Zhao, Jiawei He, Tao Qiu, Haoyu Zhang, Li Liao, Xiaoxia Su

Abstract readReview
In one paragraph

Review in Stem cell research & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
–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

27 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  19. Metformin and bone metabolism: unraveling their direct and indirect effects.Therapeutic advances in endocrinology and metabolism · 2025
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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

6 authors.

Yi ZhaoState Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Pediatrics & National Engineering Laboratory for Oral Regenerative Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Jiawei HeState Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Pediatrics & National Engineering Laboratory for Oral Regenerative Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Tao QiuState Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Pediatrics & National Engineering Laboratory for Oral Regenerative Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Haoyu ZhangState Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Pediatrics & National Engineering Laboratory for Oral Regenerative Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Li LiaoState Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Pediatrics & National Engineering Laboratory for Oral Regenerative Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Xiaoxia SuState Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Pediatrics & National Engineering Laboratory for Oral Regenerative Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu, China. orthodontist_su@163.com.ORCID 0000-0003-3612-0218

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As global aging accelerates, the prevention and treatment of age-related bone diseases are becoming a critical issue. In the process of senescence, bone marrow mesenchymal stem cells (BMSCs) gradually lose the capability of self-renewal and functional differentiation, resulting in impairment of bone tissue regeneration and disorder of bone tissue homeostasis. Alteration in epigenetic modification is an essential factor of BMSC dysfunction during aging. Its transferability and reversibility provide the possibility to combat BMSC aging by reversing age-related modifications. Emerging evidence demonstrates that epigenetic therapy based on aberrant epigenetic modifications could alleviate the senescence and dysfunction of stem cells. This review summarizes potential therapeutic targets for BMSC aging, introduces some potential approaches to alleviating BMSC aging, and analyzes its prospect in the clinical application of age-related bone diseases.

Indexed as

Bone DiseasesMesenchymal Stem CellsBone Marrow CellsBone RegenerationCell DifferentiationEpigenesis, GeneticHumansOsteogenesisAge-related bone diseasesAgingEpigeneticsMesenchymal stem cell (MSC)Therapy

Identifiers

PMID35578312
PMCPMC9109405

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.