Evidence map›Paper›PMID 25867119›Full record

ArticleCell proliferation2015

Icariin induces osteogenic differentiation of bone mesenchymal stem cells in a MAPK-dependent manner.

Yuqiong Wu, Lunguo Xia, Yuning Zhou, Yuanjin Xu, Xinquan Jiang

Abstract read
In one paragraph

Article in Cell proliferation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
13.2field-weighted citation impact, top 1% 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

69 citing papers in PubMed, 119 citations in OpenAlex.

  1. Review
  2. Review
  3. The Mechanism of Icariin in Regulating BMSCs for Treating Osteoporosis: A Review.Endocrine, metabolic & immune disorders drug targets · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. American journal of translational research · 2025
    Article
  9. Frontiers in pharmacology · 2025
    Article
  10. Article
  11. Article
  12. The Role of Herbal Medicine in Modulating Bone Homeostasis.Current topics in medicinal chemistry · 2024
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. The potential of plant extracts in cell therapy.Stem cell research & therapy · 2022
    Review
  20. Review

9 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Yuqiong WuDepartment of Prosthodontics, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200011, China; Oral Bioengineering and Regenerative Medicine Lab, Shanghai Research Institute of Stomatology, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology, Shanghai, 200011, China.
Lunguo Xia
Yuning Zhou
Yuanjin Xu
Xinquan Jiang
Shanghai Ninth People's Hospital · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIcariin, a flavonoid isolated from Epimedium pubescens, has previously been identified to exert beneficial effects on preventing bone loss and promoting bone regeneration. However, molecular mechanisms for its anabolic action have, up to now, remained largely unknown. MATERIALS AND

methodsEffects of icariin on cell proliferation and osteogenic differentiation of rat bone mesenchymal stem cells (BMSCs) were systematically evaluated. To characterize underlying mechanisms, its effects on mitogen-activated protein kinase (MAPK) signalling pathways were determined.

resultsResults showed that icariin might not have enhanced effects on cell proliferation. However, it seemed to significantly enhance osteogenic differentiation of BMSCs, demonstrated by increasing alkaline phosphatase (ALP) activity and gene expression of collagen type I (Col I), osteocalcin (OCN) and osteopotin (OPN). It was demonstrated that icariin rapidly phosphorylated extracellular signal-regulated kinase (ERK), p38 kinase and c-Jun N terminal kinase (JNK). Furthermore, icariin-stimulated osteogenic effects on BMSCs were dramatically attenuated by treatment with either specific ERK inhibitor of PD98059, p38 inhibitor of SB202190 or JNK inhibitor SP600125.

conclusionsThese results provide a potential mechanism of anabolic activity of icariin on BMSCs involving ERK, p38 and JNK MAPK pathways.

Indexed as

Alkaline PhosphataseAnimalsAnthracenesBone Density Conservation AgentsCell DifferentiationCell ProliferationCollagen Type IDrugs, Chinese HerbalExtracellular Signal-Regulated MAP KinasesFlavonoidsGene Expression Regulation, DevelopmentalImidazolesJNK Mitogen-Activated Protein KinasesMaleMesenchymal Stem CellsOsteoblasts2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazoleAlkaline PhosphataseAnthracenesBone Density Conservation AgentsCollagen Type IDrugs, Chinese HerbalExtracellular Signal-Regulated MAP KinasesFlavonoidsicariinImidazolesJNK Mitogen-Activated Protein KinasesOsteocalcinOsteopontinp38 Mitogen-Activated Protein KinasesProtein Kinase InhibitorspyrazolanthronePyridinesSpp1 protein, rat

Identifiers

PMID25867119
PMCPMC6496185
OpenAlexW2150026598

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.