Evidence map›Paper›PMID 28765584›Full record

ArticleScientific reports2017

Oleanolic Acid Enhances Mesenchymal Stromal Cell Osteogenic Potential by Inhibition of Notch Signaling.

Bing Shu, Yongjian Zhao, Yongjun Wang, Guangxi Wang, Xifu Shang, Michael Britt, Margaret Olmedo, Marjorie Chelly, Massimo Max Morandi, Shane Barton and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 29 citations in OpenAlex.

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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

11 authors at 4 institutions in 2 countries.

Bing ShuLonghua Hospital and Key Laboratory of Ministry of Education of China, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Yongjian ZhaoLonghua Hospital and Key Laboratory of Ministry of Education of China, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Yongjun WangLonghua Hospital and Key Laboratory of Ministry of Education of China, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Guangxi WangDepartment of Orthopedic Surgery, LSU Health Sciences Center, Shreveport, LA, USA.
Xifu ShangDepartment of Orthopedic Surgery, Anhui Provincial Hospital, Hefei, Anhui, China.
Michael BrittDepartment of Orthopedic Surgery, LSU Health Sciences Center, Shreveport, LA, USA.
Margaret OlmedoDepartment of Orthopedic Surgery, LSU Health Sciences Center, Shreveport, LA, USA.
Marjorie ChellyDepartment of Orthopedic Surgery, LSU Health Sciences Center, Shreveport, LA, USA.
Massimo Max MorandiDepartment of Orthopedic Surgery, LSU Health Sciences Center, Shreveport, LA, USA.
Shane BartonDepartment of Orthopedic Surgery, LSU Health Sciences Center, Shreveport, LA, USA.
Yufeng DongLonghua Hospital and Key Laboratory of Ministry of Education of China, Shanghai University of Traditional Chinese Medicine, Shanghai, China. ydong@lsuhsc.edu.
Louisiana State University Health Sciences Center Shreveport · USLonghua Hospital Shanghai University of Traditional Chinese Medicine · CNAnhui Provincial Hospital · CNShanghai University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oleanolic acid (OA), a pentacyclic triterpenoid, has been shown to modulate multiple signaling pathways in a variety of cell linages. But the mechanisms underlying OA-mediated mesenchymal stromal cell (MSC) osteogenic differentiation are not known. In this study, we examined effects of OA on cell viability, osteogenic differentiation in MSCs, and the involvement of Notch and BMP signaling. OA induced bone marrow derived MSC differentiation towards osteoprogenitor cells and inhibited Notch signaling in a dose dependent manner. Constitutive activation of Notch signaling fully blocked OA induced MSC osteogenic differentiation. The expression level of early osteogenic marker genes, ALP, Runx2, and type I collagen, which play a critical role in MSC to osteoblast transition and servers as a downstream target of BMP signaling, was significantly induced by OA. Furthermore, BMP2 mediated MSC osteogenic differentiation was significantly enhance by OA treatment, indicating a synergistic effect between BMP2 and OA. Our results suggest that OA is a promising bioactive agent for bone tissue regeneration, and inhibition of Notch signaling is required for its osteogenic effects on MSCs.

Indexed as

Cell DifferentiationCells, CulturedCell SurvivalGene Expression ProfilingHumansMesenchymal Stem CellsOleanolic AcidOsteogenesisReceptors, NotchSignal TransductionOleanolic AcidReceptors, Notch

Identifiers

PMID28765584
PMCPMC5539294
OpenAlexW2737644167

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.