Evidence map›Paper›PMID 40001240›Full record

ArticleStem cell research & therapy2025

Reducing PDK4 level constitutes a pivotal mechanism for glucocorticoids to impede osteoblastic differentiation through the enhancement of ferroptosis in mesenchymal stem cells.

Yue Jiang, Ai-Hua Ye, Wen-Ge He, Lu Liu, Xiang Gao, Hang Liu, Wen-Ting Liu, Fang-Lin Ye, Dong-Mei He, Jun-Yi Liao and 2 more

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Glucose metabolism in osteoporosis: A potential therapeutic target (Review).International journal of molecular medicine · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Impact of aging on CD146Frontiers in bioengineering and biotechnology · 2026
    Article
  10. Review
  11. Article
  12. Article
  13. Vitamin KDrug design, development and therapy · 2025
    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

12 authors.

Yue Jiang *Department of Pharmacology, School of Pharmacy, Chongqing Medical University, No. 1 Yixueyuan Road, Yuzhong District, Chongqing, 400016, People's Republic of China.
Ai-Hua Ye *Department of Pharmacology, School of Pharmacy, Chongqing Medical University, No. 1 Yixueyuan Road, Yuzhong District, Chongqing, 400016, People's Republic of China.
Wen-Ge He *Key Laboratory of Biochemistry and Molecular Pharmacology of Chongqing, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Lu LiuDepartment of Pharmacology, School of Pharmacy, Chongqing Medical University, No. 1 Yixueyuan Road, Yuzhong District, Chongqing, 400016, People's Republic of China.
Xiang GaoKey Laboratory of Biochemistry and Molecular Pharmacology of Chongqing, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Hang LiuKey Laboratory of Biochemistry and Molecular Pharmacology of Chongqing, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Wen-Ting LiuDepartment of Pharmacology, School of Pharmacy, Chongqing Medical University, No. 1 Yixueyuan Road, Yuzhong District, Chongqing, 400016, People's Republic of China.
Fang-Lin YeDepartment of Pharmacology, School of Pharmacy, Chongqing Medical University, No. 1 Yixueyuan Road, Yuzhong District, Chongqing, 400016, People's Republic of China.
Dong-Mei HeDepartment of Pharmacology, School of Pharmacy, Chongqing Medical University, No. 1 Yixueyuan Road, Yuzhong District, Chongqing, 400016, People's Republic of China.
Jun-Yi LiaoDepartment of Bone and Soft Tissue Oncology, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Jing WangDepartment of Blood Transfusion, the First Affiliated Hospital of Chongqing Medical University, No. 1 Youyi Road, Yuzhong District, Chongqing, 400016, People's Republic of China. wjsy86@hospital.cqmu.edu.cn.
Bai-Cheng HeDepartment of Pharmacology, School of Pharmacy, Chongqing Medical University, No. 1 Yixueyuan Road, Yuzhong District, Chongqing, 400016, People's Republic of China. bche@cqmu.edu.cn.

Funding

Chongqing Science and Technology Commission Project CSTB2023NSCQ-MSX0151the National Natural Science Foundation of China 81572226
6 · The paper itself

Abstract

backgroundThis study mainly explores the possible role and mechanism of pyruvate dehydrogenase kinase 4 (PDK4) in the onset and development of Glucocorticoid-induced osteoporosis (GIOP), and seeks potential targets for the treatment of GIOP.

methodsMesenchymal stem cells (MSCs) were treated with osteogenic induction medium. An in vitro osteogenic damage model was established by exposing MSCs to a high concentration (10

resultsHigh concentrations (10

conclusionPDK4 can enhance the osteogenic differentiation ability of MSCs and bone mass of GIOP rats. DEX may promote the degradation of PDK4 via lysosome pathway, through which to weaken the osteogenic ability of MSCs by increasing ferroptosis. PDK4 may become a potential target for improving GIOP.

Indexed as

Cell DifferentiationFerroptosisGlucocorticoidsMesenchymal Stem CellsOsteoblastsPyruvate Dehydrogenase Acetyl-Transferring KinaseAnimalsCell LineDexamethasoneMaleMiceOsteogenesisOsteoporosisProtein KinasesRatsRats, Sprague-DawleyDexamethasoneGlucocorticoidsPdk4 protein, ratProtein KinasesPyruvate Dehydrogenase Acetyl-Transferring Kinasepyruvate dehydrogenase kinase 4Reactive Oxygen SpeciesDexamethasoneFerroptosisGlucocorticoid-induced osteoporosis (GIOP)Osteogenic differentiationPyruvate dehydrogenase kinase 4

Identifiers

PMID40001240
PMCPMC11863902

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.