Evidence map›Paper›PMID 31612613›Full record

ArticleJournal of cellular and molecular medicine2019

Asperpyrone A attenuates RANKL-induced osteoclast formation through inhibiting NFATc1, Ca

Xi Chen, Chao Wang, Heng Qiu, Yu Yuan, Kai Chen, Zhen Cao, Ren Xiang Tan, Jennifer Tickner, Jiake Xu, Jun Zou

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

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  14. MT2 INHIBITS OSTEOCLASTOGENESIS BY SCAVENGING ROS.Acta endocrinologica (Bucharest, Romania : 2005)
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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

10 authors at 3 institutions in 2 countries.

Xi ChenSchool of Sports Science, Wenzhou Medical University, Wenzhou, China.ORCID 0000-0001-8374-8054
Chao WangSchool of Biomedical Sciences, University of Western Australia, Perth, Western Australia, Australia.
Heng QiuSchool of Biomedical Sciences, University of Western Australia, Perth, Western Australia, Australia.
Yu YuanSchool of Biomedical Sciences, University of Western Australia, Perth, Western Australia, Australia.
Kai ChenSchool of Biomedical Sciences, University of Western Australia, Perth, Western Australia, Australia.
Zhen CaoSchool of Biomedical Sciences, University of Western Australia, Perth, Western Australia, Australia.
Ren Xiang TanState Key Laboratory of Pharmaceutical Biotechnology, Institute of Functional Biomolecules, Nanjing University, Nanjing, China.
Jennifer TicknerSchool of Biomedical Sciences, University of Western Australia, Perth, Western Australia, Australia.
Jiake XuSchool of Kinesiology, Shanghai University of Sport, Shanghai, China.ORCID 0000-0003-2021-8309
Jun ZouSchool of Kinesiology, Shanghai University of Sport, Shanghai, China.ORCID 0000-0001-6036-8067
The University of Western Australia · AUNanjing University · CNShanghai University of Sport · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Imbalance of osteoblast and osteoclast in adult leads to a variety of bone-related diseases, including osteoporosis. Thus, suppressing the activity of osteoclastic bone resorption becomes the main therapeutic strategy for osteoporosis. Asperpyrone A is a natural compound isolated from Aspergillus niger with various biological activities of antitumour, antimicrobial and antioxidant. The present study was designed to investigate the effects of Asperpyrone A on osteoclastogenesis and to explore its underlining mechanism. We found that Asperpyrone A inhibited RANKL-induced osteoclastogenesis in a dose-dependent manner when the concentration reached 1 µm, and with no cytotoxicity until the concentration reached to 10 µm. In addition, Asperpyrone A down-regulated the mRNA and protein expression of NFATc1, c-fos and V-ATPase-d2, as well as the mRNA expression of TRAcP and Ctsk. Furthermore, Asperpyrone A strongly attenuated the RNAKL-induced intracellular Ca

Indexed as

AnimalsAspergillus nigerBiological ProductsCalciumCalcium SignalingCells, CulturedGene ExpressionIntracellular SpaceMiceMice, Inbred C57BLMolecular StructureNaphthalenesNFATC Transcription FactorsOsteoclastsOsteogenesisOxidative Stressasperpyrone ABiological ProductsCalciumNaphthalenesNFATC Transcription FactorsPyronesRANK LigandReactive Oxygen SpeciesTartrate-Resistant Acid PhosphataseAsperpyrone ACa2+ signallingosteoclastosteoporosisreactive oxygen species

Identifiers

PMID31612613
PMCPMC6850946
OpenAlexW2980508439

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.