Evidence map›Paper›PMID 41272063›Full record

ArticleScientific reports2025

Resveratrol delays senescence of human dental pulp stem cells via activating the SIRT1-mitochondrial autophagy.

Zelu Li, Xiaoyang Chu, Jiahao Guo, Yulan Xiang, Yingyi Luan, Hongcheng Xing, Xixi Lv, Yanhong Zhou, Kai Yang, Yang Zeng and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Phenotyping of Human Pulp Cells After Cryopreservation.Journal of cellular and molecular medicine · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
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.

Zelu Li *Department of Orthodontics, Beijing Stomatological Hospital, Capital Medical University School of Stomatology, Capital Medical University, Beijing, China.
Xiaoyang Chu *Department of Stomatology, Fifth Medical Center of Chinese, PLA General Hospital, Beijing, China.
Jiahao Guo *School of Life Science and Technology, Shandong Second Medical University, Weifang, Shandong, China.
Yulan XiangDepartment of Orthodontics, Beijing Stomatological Hospital, Capital Medical University School of Stomatology, Capital Medical University, Beijing, China.
Yingyi LuanPrenatal Diagnosis Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China.
Hongcheng XingDepartment of Orthodontics, Beijing Stomatological Hospital, Capital Medical University School of Stomatology, Capital Medical University, Beijing, China.
Xixi LvDepartment of Orthodontics, Beijing Stomatological Hospital, Capital Medical University School of Stomatology, Capital Medical University, Beijing, China.
Yanhong ZhouDepartment of Orthodontics, Beijing Stomatological Hospital, Capital Medical University School of Stomatology, Capital Medical University, Beijing, China.
Kai YangSchool of Life Science and Technology, Shandong Second Medical University, Weifang, Shandong, China. yk19830919@ccmu.edu.cn.
Yang ZengSenior Department of Hematology, Fifth Medical Center of Chinese, PLA General Hospital, Beijing, China. zengzengyang89@126.com.
Dongliang ZhangDepartment of Orthodontics, Beijing Stomatological Hospital, Capital Medical University School of Stomatology, Capital Medical University, Beijing, China. zhangdongliang@mail.ccmu.edu.cn.

Funding

Beijing Nova Program 20230484404Funds of Beijing Obstetrics and Gynecology Hospital, Capital Medical University no. FCYYJC202403National Key R&D Program of China 2022YFA1106300the Capital's Funds for Health Improvement and Research no. SHOUFA 2024-2-2143the National Natural Science Foundation of China 82370108Young Elite Scientists Sponsorship Program by CAST 2022QNRC001
6 · The paper itself

Abstract

Human dental pulp stem cells (hDPSCs) senescence impairs their proliferation and osteogenic differentiation, critical for dental stem cell therapy. This study evaluated the effects of Resveratrol on the senescence of hDPSCs to explore new therapeutic strategies. Metabolomic analysis identified age-related metabolic differences in dental pulp tissues, with enriched pathways linked to Resveratrol. In vitro, Resveratrol improved proliferation, delayed senescence, promoted osteogenic differentiation, and enhanced mitochondrial autophagy, function, and biogenesis in senescent hDPSCs, reducing mitochondrial damage and oxidative stress. Mechanistically, silencing PINK1 or PGC-1α reversed Resveratrol-mediated promotion of proliferation, osteogenesis, and senescence suppression. Blocking SIRT1 abrogated its effects on mitochondrial quality control. These findings highlight Resveratrol's potential to mitigate hDPSCs senescence via SIRT1-dependent mitochondrial regulation, offering insights for age-related dental regenerative therapies.

Indexed as

AutophagyCellular SenescenceDental PulpMitochondriaResveratrolSirtuin 1Stem CellsCell DifferentiationCell ProliferationCells, CulturedHumansOsteogenesisOxidative StressPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaProtein KinasesPTEN-Induced Putative KinasePeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaProtein KinasesPTEN-Induced Putative KinaseResveratrolSIRT1 protein, humanSirtuin 1hDPSCsPINK1 and PGC-1αResveratrolSenescenceSIRT1

Identifiers

PMID41272063
PMCPMC12639125

What OpenQuestion holds

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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.