Evidence map›Paper›PMID 26690415›Full record

ArticleInternational journal of molecular sciences2015

Calycosin Suppresses RANKL-Mediated Osteoclastogenesis through Inhibition of MAPKs and NF-κB.

Gui-Hua Quan, Hongbing Wang, Jinjin Cao, Yuxin Zhang, Donglin Wu, Qisheng Peng, Ning Liu, Wan-Chun Sun

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

39 citing papers in PubMed, 58 citations in OpenAlex.

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  13. AS-605240 Blunts Osteoporosis by Inhibition of Bone Resorption.Drug design, development and therapy · 2023
    Article
  14. Article
  15. Review
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  17. Article
  18. Review
  19. Article
  20. Pharmaceutical Values of Calycosin: One Type of Flavonoid Isolated fromEvidence-based complementary and alternative medicine : eCAM · 2021
    Review
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

8 authors at 3 institutions in 1 country.

Gui-Hua QuanKey Laboratory for Molecular and Chemical Genetics of Critical Human Diseases of Jilin Province, Jilin University Bethune Second Hospital, Changchun 130041, China. qgh0521@jlu.edu.cn.
Hongbing WangSchool of Life Sciences and Technology, Tongji University, Shanghai 200092, China. hbwang@tongji.edu.cn.
Jinjin CaoKey laboratory of Zoonosis, Ministry of Education, Institute of Zoonosis, Jilin University, Changchun 130062, China. jinjincao90@163.com.
Yuxin ZhangKey laboratory of Zoonosis, Ministry of Education, Institute of Zoonosis, Jilin University, Changchun 130062, China. chongfengxing@163.com.
Donglin WuDepartment of Virus Disease Prevention and Control, Jilin Provincial Center for Disease Control and Prevention, Changchun 130062, China. dl_wu@163.com.
Qisheng PengKey laboratory of Zoonosis, Ministry of Education, Institute of Zoonosis, Jilin University, Changchun 130062, China. pengqs@jlu.edu.cn.
Ning LiuKey Laboratory for Molecular and Chemical Genetics of Critical Human Diseases of Jilin Province, Jilin University Bethune Second Hospital, Changchun 130041, China. liu_ning@jlu.edu.cn.
Wan-Chun SunKey laboratory of Zoonosis, Ministry of Education, Institute of Zoonosis, Jilin University, Changchun 130062, China. wanchunsun@jlu.edu.cn.
Jilin University · CNBethune Second Hospital · CNTongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calycosin, an isoflavonoid phytoestrogen, isolated from Radix Astragali, was reported to possess anti-tumor, anti-inflammation, and osteogenic properties, but its impact on osteoclast differentiation remains unclear. In this study, we examined the effects of calycosin on osteoclastogenesis induced by RANKL. The results showed that calycosin significantly inhibited RANKL-induced osteoclast formation from primary bone marrow macrophages (BMMs). Calycosin also dose-dependently suppressed the formation of bone resorption pits by mature osteoclasts. In addition, the expression of osteoclatogenesis-related genes, including cathepsin K (CtsK), tartrate-resistant acid phosphatase (TRAP), and MMP-9, was significantly inhibited by calycosin. Furthermore, the results indicated that calycosin down-regulated the expression levels of NFATc1 and c-Fos through suppressing the activation of NF-κB and MAPKs. Our results indicate that calycosin has an inhibitory role in the bone loss by preventing osteoclast formation, as well as its bone resorptive activity. Therefore, calycosin may be useful as a therapeutic reagent for bone loss-associated diseases.

Indexed as

AnimalsBone ResorptionCell DifferentiationCells, CulturedGene ExpressionIsoflavonesMacrophagesMaleMAP Kinase Signaling SystemMice, Inbred C57BLMitogen-Activated Protein KinasesNFATC Transcription FactorsNF-kappa BOsteoclastsPhosphorylationProtein Processing, Post-Translational7,3'-dihydroxy-4'-methoxyisoflavoneIsoflavonesMitogen-Activated Protein KinasesNfatc1 protein, mouseNFATC Transcription FactorsNF-kappa BProto-Oncogene Proteins c-fosRANK LigandTnfsf11 protein, mousebone resorptioncalycosinc-FosMAPKsNFATc1NF-κBosteoclast

Identifiers

PMID26690415
PMCPMC4691122
OpenAlexW2191914461

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.