Evidence map›Paper›PMID 32939977›Full record

ArticleJournal of cellular and molecular medicine2020

Maackiain dampens osteoclastogenesis via attenuating RANKL-stimulated NF-κB signalling pathway and NFATc1 activity.

Yuhao Liu, Weizai Zeng, Chao Ma, Ziyi Wang, Chao Wang, Shaobin Li, Wei He, Qingwen Zhang, Jiake Xu, Chi Zhou

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Implications of enolase in the RANKL-mediated osteoclast activity following spinal cord injury.Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2021
    Article
  7. The Pathophysiology of Osteoporosis after Spinal Cord Injury.International journal of molecular sciences · 2021
    Review
  8. Article
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 2 institutions in 2 countries.

Yuhao LiuThe First Affiliated Hospital, Institute of Orthopedics, Guangzhou University of Chinese Medicine, Guangzhou, China.ORCID 0000-0002-0447-6677
Weizai ZengChinese Medicine Hospital of Zengcheng District, Guangzhou, China.
Chao MaThe First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, China.
Ziyi WangSchool of Biomedical Sciences, University of Western Australia, Perth, Australia.
Chao WangSchool of Biomedical Sciences, University of Western Australia, Perth, Australia.
Shaobin LiThe First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, China.
Wei HeThe First Affiliated Hospital, Institute of Orthopedics, Guangzhou University of Chinese Medicine, Guangzhou, China.
Qingwen ZhangThe First Affiliated Hospital, Institute of Orthopedics, Guangzhou University of Chinese Medicine, Guangzhou, China.
Jiake XuThe First Affiliated Hospital, Institute of Orthopedics, Guangzhou University of Chinese Medicine, Guangzhou, China.ORCID 0000-0003-2021-8309
Chi ZhouThe First Affiliated Hospital, Institute of Orthopedics, Guangzhou University of Chinese Medicine, Guangzhou, China.ORCID 0000-0003-1905-9494
Guangzhou University of Chinese Medicine · CNThe University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteolytic diseases are typified by over-enhanced formation and resorbing function of osteoclasts and have a major impact on human health. Inhibition of osteoclastic differentiation and function is a key strategy for clinical therapy of osteolytic conditions. Maackiain is a natural compound extracted from Sophora flavescens, which has been applied to anti-allergic and anti-tumour treatments. The present results showed that Maackiain could restrain receptor activator of nuclear factor-κB ligand (RANKL)-stimulated osteoclast formation and hydroxyapatite resorption dose-dependently, and interrupt the structures of F-actin belts in the mature osteoclasts. It also repressed the expressions of osteoclast-specific genes and proteins. Furthermore, Maackiain could inhibit RANKL-stimulated NF-κB and calcium signalling pathways, and dampen Nuclear factor of activated T cell cytoplasmic 1 activity, protein expression and translocation into the nucleus. These results revealed that Maackiain may have a potential therapeutic effect on osteoclast-related disorders.

Indexed as

Active Transport, Cell NucleusAnimalsBone Marrow CellsBone ResorptionCalciumCell DifferentiationCell SurvivalFemaleGene Expression RegulationMacrophagesMiceNFATC Transcription FactorsNF-kappa BOsteoblastsOsteoclastsOsteogenesisCalciuminerminNfatc1 protein, mouseNFATC Transcription FactorsNF-kappa BPhytoalexinsPterocarpansRANK LigandTnfsf11 protein, mousemaackiainnuclear factor of activated T cells 1nuclear factor-κBosteoclastreceptor activator of nuclear factor-κB ligand

Identifiers

PMID32939977
PMCPMC7686960
OpenAlexW3087523105

What OpenQuestion holds

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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.