Evidence map›Paper›PMID 29264750›Full record

ArticleJournal of bone and mineral metabolism2018

Study of the osteogenesis effect of icariside II and icaritin on canine bone marrow mesenchymal stem cells.

Guangming Luo, Biao Xu, Weihong Wang, Yong Wu, Ming Li

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of bone and mineral metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. A comprehensive narrative review ofJournal of pharmaceutical analysis · 2026
    Review
  2. Involvement of icaritin in the regulation of osteocyte exosomal microRNAs.Journal of orthopaedic surgery and research · 2025
    Article
  3. Article
  4. Review
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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

5 authors at 2 institutions in 1 country.

Guangming LuoDepartment of Oral and Maxillofacial Surgery, Affiliated Stomatology Hospital of Kunming Medical University, Block C No 1088 of Hai Yuan Road, High and New Technology Zone, Kunming, 650031, Yunnan, People's Republic of China. 1719663004@qq.com.
Biao XuDepartment of Oral and Maxillofacial Surgery, Affiliated Stomatology Hospital of Kunming Medical University, Block C No 1088 of Hai Yuan Road, High and New Technology Zone, Kunming, 650031, Yunnan, People's Republic of China.
Weihong WangDepartment of Oral and Maxillofacial Surgery, Affiliated Stomatology Hospital of Kunming Medical University, Block C No 1088 of Hai Yuan Road, High and New Technology Zone, Kunming, 650031, Yunnan, People's Republic of China.
Yong WuDepartment of Oral and Maxillofacial Surgery, Affiliated Stomatology Hospital of Kunming Medical University, Block C No 1088 of Hai Yuan Road, High and New Technology Zone, Kunming, 650031, Yunnan, People's Republic of China.
Ming LiDepartment of Oral and Maxillofacial Surgery, Affiliated Stomatology Hospital of Kunming Medical University, Block C No 1088 of Hai Yuan Road, High and New Technology Zone, Kunming, 650031, Yunnan, People's Republic of China.
Stomatology Hospital · CNKunming Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to identify the osteogenesis effect of icariside II (ICSII) and icaritin (ICT) in vitro. Bone marrow mesenchymal stem cells (BMSCs) were treated with ICSII and ICT in order to detect the proliferation and differentiation of BMSCs, the expression of the osteogenesis-related proteins with or without osteogenic medium (OM) and genes, Runt-related transcription factor 2 (Runx-2), osteocalcin (OCN), osteopontin (OPN), osterix, and basic fibroblast growth factor (bFGF), and the phosphorylation levels of mitogen-activated protein kinase (MAPK). We found that the optical density increased and alkaline phosphatase decreased after the BMSCs were treated with different concentrations of ICSII; however, ICT showed an opposing effect. The formation of calcium nodules was observed after the BMSCs were treated with ICSII and ICT. The expression level of osteogenesis-related proteins was enhanced following treatment with both ICSII or ICT, while the expression level of the osteogenesis-related genes Runx-2, OCN, OPN, osterix, and bFGF significantly increased with ICSII treatment (P < 0.05), and only Runx-2 and bFGF significantly increased (P < 0.01) with ICT. The expression of osteogenic differentiation-related proteins (except OPN) following treatment with ICSII + OM or ICT + OM was not notably increased. Both ICSII and ICT elevated the phosphorylation levels of MAPK/ERK, which was attenuated by GDC-0994 (an inhibitor of MAPK/ERK). Collectively, these data indicate that ICSII and ICT facilitate orientation osteogenic differentiation of BMSCs, which is most likely via the MAPK/ERK pathway. OM did not synergistically enhance the osteogenesis effect of ICSII and ICT.

Indexed as

OsteogenesisAnimalsCalciumCell DifferentiationCell ProliferationCells, CulturedCell ShapeDogsFlavonoidsGene Expression RegulationMAP Kinase Signaling SystemMesenchymal Stem Cellsbaohuoside ICalciumFlavonoidsicaritinBone marrow mesenchymal stem cellsIcariside IIIcaritin

Identifiers

PMID29264750
OpenAlexW2776027271

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.