Evidence map›Paper›PMID 31331121›Full record

ArticleMolecules (Basel, Switzerland)2019

Betulin Promotes Differentiation of Human Osteoblasts In Vitro and Exerts an Osteoinductive Effect on the hFOB 1.19 Cell Line Through Activation of JNK, ERK1/2, and mTOR Kinases.

Magdalena Mizerska-Kowalska, Adrianna Sławińska-Brych, Katarzyna Kaławaj, Aleksandra Żurek, Beata Pawińska, Wojciech Rzeski, Barbara Zdzisińska

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
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  7. mTOR Signaling Pathway in Bone Diseases Associated with Hyperglycemia.International journal of molecular sciences · 2023
    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

7 authors at 1 institution in 1 country.

Magdalena Mizerska-KowalskaDepartment of Virology and Immunology; Maria Curie-Sklodowska University, Lublin 20-033, Poland. magdalena.mizerska-dudka@poczta.umcs.lublin.pl.ORCID 0000-0003-2364-6181
Adrianna Sławińska-BrychDepartment of Cell Biology, Maria Curie-Sklodowska University, Lublin 20-033, Poland.
Katarzyna KaławajDepartment of Virology and Immunology; Maria Curie-Sklodowska University, Lublin 20-033, Poland.
Aleksandra ŻurekDepartment of Virology and Immunology; Maria Curie-Sklodowska University, Lublin 20-033, Poland.
Beata PawińskaDepartment of Virology and Immunology; Maria Curie-Sklodowska University, Lublin 20-033, Poland.
Wojciech RzeskiDepartment of Virology and Immunology; Maria Curie-Sklodowska University, Lublin 20-033, Poland.
Barbara ZdzisińskaDepartment of Virology and Immunology; Maria Curie-Sklodowska University, Lublin 20-033, Poland. basiaz@poczta.umcs.lublin.pl.ORCID 0000-0002-0920-3192
Maria Curie-Skłodowska University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although betulin (BET), a naturally occurring pentacyclic triterpene, has a variety of biological activities, its osteogenic potential has not been investigated so far. The aim of this study was to assess the effect of BET on differentiation of human osteoblasts (hFOB 1.19 and Saos-2 cells) in vitro in osteogenic (with ascorbic acid as an osteogenic supplement) and osteoinductive (without an additional osteogenic supplement) conditions. Osteoblast differentiation was evaluated based on the mRNA expression (RT-qPCR) of Runt-related transcription factor 2 (RUNX2), alkaline phosphatase (ALP), type I collagen-α1 (COL1A1), and osteopontin (OPN). Additionally, ALP activity and production of COL1A1 (western blot analysis) and OPN (ELISA) were evaluated. The level of mineralization (calcium accumulation) was determined with Alizarin red S staining. BET upregulated the mRNA level of RUNX2 and the expression of other osteoblast differentiation markers in both cell lines (except the influence of BET on ALP expression/activity in the Saos-2 cells). Moreover, it increased mineralization in both cell lines in the osteogenic conditions. BET also increased the mRNA level of osteoblast differentiation markers in both cell lines (except for ALP in the Saos-2 cells) in the osteoinductive conditions, which was accompanied with increased matrix mineralization. The osteoinductive activity of BET in the hFOB 1.19 cells was probably mediated via activation of MAPKs (JNK and ERK1/2) and mTOR, as the specific inhibitors of these kinases abolished the BET-induced osteoblast differentiation. Our results suggest that BET has the potential to enhance osteogenesis.

Indexed as

Betulinic AcidBiomarkersBone MatrixCalcification, PhysiologicCell DifferentiationCell LineCell ProliferationCells, CulturedCell SurvivalHumansMAP Kinase Signaling SystemOsteoblastsOsteogenesisRNA, MessengerTOR Serine-Threonine KinasesTriterpenesbetulinBetulinic AcidBiomarkersMTOR protein, humanRNA, MessengerTOR Serine-Threonine KinasesTriterpenesbetulindifferentiationmineralizationosteoblasts

Identifiers

PMID31331121
PMCPMC6680433
OpenAlexW2964347655

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.