Evidence map›Paper›PMID 33377656›Full record

ArticleClinical and translational medicine2020

A selected small molecule prevents inflammatory osteolysis through restraining osteoclastogenesis by modulating PTEN activity.

Yueqi Chen, Wenhui Hu, Yiran Wang, Yuheng Li, Xiaoming Li, Haibo Li, Yong Tang, Lincheng Zhang, Yutong Dong, Xiaochao Yang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  10. Inflammasomes in Alveolar Bone Loss.Frontiers in immunology · 2021
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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

12 authors at 2 institutions in 1 country.

Yueqi ChenDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, PR China.ORCID https://orcid.org/0000-0001-6975-2874
Wenhui HuDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, PR China.
Yiran WangDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, PR China.
Yuheng LiDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, PR China.
Xiaoming LiDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, PR China.
Haibo LiNational Engineering Research Center of Immunological Products & Department of Microbiology and Biochemical Pharmacy, College of Pharmacy, Third Military Medical University (Army Medical University), Chongqing, PR China.
Yong TangDepartment of Orthopaedics, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, PR China.
Lincheng ZhangDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, PR China.
Yutong DongDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, PR China.
Xiaochao YangDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, PR China.
Ye WeiSchool of Chemistry and Chemical Engineering, Southwest University, Chongqing, PR China.
Shiwu DongDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, PR China.ORCID https://orcid.org/0000-0002-5032-4893
Army Medical University · CNSouthwest University · CN

Funding

Key Program of Natural Science Foundation of China 81930067Medical innovation of graduate students in Chongqing CYS19360Medical Science and Technology Youth Cultivation Project of PLA 20QNPY022Nature Science Foundation of China 31870962
6 · The paper itself

Abstract

backgroundInflammatory osteolysis is a severe infectious bone disorder that occurs during orthopaedic surgery and is caused by disruptions in the dynamic balance of bone matrix homeostasis, which makes this condition a burden on surgical procedures. Developing novel therapeutic drugs about inhibiting excessive osteoclastogenesis acts as an efficient approach to preventing inflammatory bone destruction.

methodsTo study this, we explored the potential effects and mechanisms of compound 17 on inflammatory osteolysis in vitro. Meanwhile, a lipopolysaccharide (LPS)-induced calvarial osteolysis mouse model was used to evaluate the protective effect of compound 17 on inflammatory bone destruction in vivo.

resultsIn our study, we found that compound 17 could inhibit osteoclast (OC) differentiation and bone resorption during RANKL and LPS stimulation in a time- and dose-dependent manner, while compounds 5 and 13 did not have the same effects. Mechanistically, compound 17 promoted phosphatase and tensin homologue (PTEN) activity by reducing PTEN ubiquitination, thereby restraining the RANKL-induced NF-κB pathway, resulting in the inhibition of the expression of osteoclastogenesis-related genes and the formation of the NLRP3 inflammasome. Additionally, we also investigated whether compound 17 could negatively modulate macrophage polarization and repolarization due to its anti-inflammatory effects. Moreover, compound 17 also plays an important role in osteoblast differentiation and mineralization. In vivo experiments showed that compound 17 could effectively protect mice from LPS-induced inflammatory bone destruction by inhibiting osteoclastogenesis and inflammation.

conclusionsTaken together, these results show that compound 17 might play protective role in inflammatory bone destruction through inhibiting osteoclastogenesis and inflammation. These findings imply a possible role of compound 17 in inflammatory osteolysis-related diseases.

Indexed as

inflammatory osteolysisosteoclastogenesisPTENsmall molecule

Identifiers

PMID33377656
PMCPMC7708775
OpenAlexW3106636097

What Socratic 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 Socratic graph.