Evidence map›Paper›PMID 30900017›Full record

ArticleJournal of bone and mineral metabolism2019

miR-142-5p promotes the osteoclast differentiation of bone marrow-derived macrophages via PTEN/PI3K/AKT/FoxO1 pathway.

Zhenkai Lou, Zhi Peng, Bing Wang, Xingguo Li, Xing Li, Xinliang Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of bone and mineral metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 51 citations in OpenAlex.

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  10. Regulation of osteoclast-mediated bone resorption by microRNA.Cellular and molecular life sciences : CMLS · 2022
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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

6 authors at 4 institutions in 1 country.

Zhenkai LouDepartment of Orthopaedics, The First Affiliated Hospital of Kunming Medical University, Kunming, 650032, Yunnan, China.
Zhi PengDepartment of Spine Surgery, The First Affiliated Hospital of Dali University, Dali, 671000, Yunnan, China.
Bing WangDepartment of Orthopaedics, The First Affiliated Hospital of Kunming Medical University, Kunming, 650032, Yunnan, China.
Xingguo LiDepartment of Orthopaedics, The First Affiliated Hospital of Kunming Medical University, Kunming, 650032, Yunnan, China.
Xing LiDepartment of Ultrasonography, The First Affiliated Hospital of Kunming Medical University, Kunming, 650032, Yunnan, China.
Xinliang ZhangDepartment of Spine Surgery, Honghui Hospital, Xi'an Jiaotong University, No.76 Nanguo Rd., Xi'an City, 710054, Shanxi, China. Apoptosis110@163.com.
First Affiliated Hospital of Kunming Medical University · CNDali University · CNKunming Medical University · CNXi'an Honghui Hospital · CN

Funding

PhD scientific research fund of The First Affiliated Hospital of Kunming Medical University No. 2017BS030Scientific and technological innovation team for spine degenerative disease research of Kunming Medical University No. CXTD201805The Health Science and Technology Project of Yunnan province No.2016NS021The Health Science and Technology Project of Yunnan province No.2017NS021The Health Science and Technology Project of Yunnan province No.2017NS022The National Natural Science Foundation of China No.81760029The National Natural Science Foundation of China No.81760030
6 · The paper itself

Abstract

It is increasingly recognized that microRNAs (miRNAs) are a kind of important regulators, which are involved in the pathogenesis and development of various human diseases. However, the underlying effects and mechanism of miR-142-5p on the osteoclast differentiation of bone marrow-derived macrophages (BMMs) have not been elucidated. The aim of the present study is to explore the molecular mechanisms that regulate the osteoclastogenesis of BMMs for providing more efficient methods for treating bone-related diseases. In the present study, BMMs were isolated from rats and cultured. Moreover, receptor activators of NF-kB ligands were used to induce the osteoclast differentiation of BMMs. Furthermore, we analyzed the effects of miR-142-5p mimics/inhibitor on the osteoclastogenesis of BMMs. The results indicated that the downregulation of miR-142-5p inhibited the osteoclastogenesis of BMMs, whereas the overexpression enhanced this process. PTEN was testified to be a direct target of miR-142-5p, and its effects on the osteoclastogenesis were also described. Most importantly, treatment of LY29004 (an inhibitor of the PI3k/Akt pathway) can attenuate miR-142-5p osteoclastogenesis effects, while the inhibition effects of LY29004 on the osteoclastogenesis were abolished by knockdown of FoxO1. Taken together, our findings demonstrated that miR-142-5p promotes the osteoclastogenesis of BMMs through PI3k/Akt/FoxO1 pathway via targeting PTEN.

Indexed as

AnimalsBase SequenceCell DifferentiationDown-RegulationForkhead Box Protein O1HumansMacrophage Colony-Stimulating FactorMacrophagesMicroRNAsOsteoclastsOsteogenesisPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseRANK LigandRats, Sprague-DawleyForkhead Box Protein O1Macrophage Colony-Stimulating FactorMicroRNAsMIRN142 microRNA, ratPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePten protein, ratRANK LigandBone marrow-derived macrophagesFoxO1miR-142-5pOsteoclastPTEN

Identifiers

PMID30900017
OpenAlexW2923553387

What OpenQuestion holds

Textmetadata
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.