Evidence map›Paper›PMID 30291236›Full record

ArticleNature communications2018

Bone protection by inhibition of microRNA-182.

Kazuki Inoue, Zhonghao Deng, Yufan Chen, Eugenia Giannopoulou, Ren Xu, Shiaoching Gong, Matthew B Greenblatt, Lingegowda S Mangala, Gabriel Lopez-Berestein, David G Kirsch and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 2 pooled it
4.8field-weighted citation impact, top 4% 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

53 citing papers in PubMed, 2 syntheses or guidelines pooled it, 95 citations in OpenAlex.

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  10. Roles of naïve CD4Journal of translational medicine · 2024
    Article
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  12. [Research Progress in the Regulatory Role of circRNA-miRNA Network in Bone Remodeling].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2024
    Review
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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

13 authors at 6 institutions in 2 countries.

Kazuki InoueArthritis and Tissue Degeneration Program, The David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, 10021, NY, USA.
Zhonghao DengArthritis and Tissue Degeneration Program, The David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, 10021, NY, USA.
Yufan ChenDepartment of Orthopedic Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Eugenia GiannopoulouArthritis and Tissue Degeneration Program, The David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, 10021, NY, USA.
Ren XuDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, 10065, NY, USA.ORCID http://orcid.org/0000-0001-6578-4553
Shiaoching GongDepartment of Molecular Biology, The Rockefeller University, New York, 10065, NY, USA.
Matthew B GreenblattDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, 10065, NY, USA.
Lingegowda S MangalaDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, 77030, TX, USA.
Gabriel Lopez-BeresteinCenter for RNA Interference and Noncoding RNA, The University of Texas MD Anderson Cancer Center, Houston, 77030, TX, USA.
David G KirschDepartment of Radiation Oncology and Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, 27710, NC, USA.
Anil K SoodDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, 77030, TX, USA.
Liang ZhaoDepartment of Orthopedic Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Baohong ZhaoArthritis and Tissue Degeneration Program, The David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, 10021, NY, USA. zhaob@hss.edu.ORCID http://orcid.org/0000-0002-1286-0919
Hospital for Special Surgery · USThe University of Texas MD Anderson Cancer Center · USCornell University · USNanfang Hospital · CNDuke Medical Center · USRockefeller University · US

Funding

Harnessing the power of exosomes for non-coding RNA deliveryR35CA209904 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SOOD, ANIL K · 2017 to 2023
$5.0M
Regulation of Osteoclastogenesis and Arthritic Bone Resorption by RBP-JR01AR071463 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI Kyung-Hyun Park-Min · 2017 to 2026
$4.0M
Modulation of Bone Formation by SHN3DP5OD021351 · OD · WEILL MEDICAL COLL OF CORNELL UNIV · PI GREENBLATT, MATTHEW BLAKE · 2015 to 2019
$2.1M
Mechanisms of inflammatory bone remodelingR01AR068970 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI ZHAO, BAOHONG · 2016 to 2021
$1.9M
"Establishing Pathways for Endothelial Support of Bone Formation with SLIT3"R01AR075585 · NIAMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI GREENBLATT, MATTHEW BLAKE · 2020 to 2024
$1.8M
Regulation of Osteoclastogenesis and Arthritic Bone Resorption by RBP-JR00AR062047 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI ZHAO, BAOHONG · 2014 to 2016
$747k
NCI NIH HHS R35 CA209904NIAMS NIH HHS R00 AR062047NIAMS NIH HHS R01 AR068970NIAMS NIH HHS R01 AR071463NIAMS NIH HHS R01 AR075585NIH HHS DP5 OD021351U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) R00 AR062047, R01 AR068970 and R01 AR071463
6 · The paper itself

Abstract

Targeting microRNAs recently shows significant therapeutic promise; however, such progress is underdeveloped in treatment of skeletal diseases with osteolysis, such as osteoporosis and rheumatoid arthritis (RA). Here, we identified miR-182 as a key osteoclastogenic regulator in bone homeostasis and diseases. Myeloid-specific deletion of miR-182 protects mice against excessive osteoclastogenesis and bone resorption in disease models of ovariectomy-induced osteoporosis and inflammatory arthritis. Pharmacological treatment of these diseases with miR-182 inhibitors completely suppresses pathologic bone erosion. Mechanistically, we identify protein kinase double-stranded RNA-dependent (PKR) as a new and essential miR-182 target that is a novel inhibitor of osteoclastogenesis via regulation of the endogenous interferon (IFN)-β-mediated autocrine feedback loop. The expression levels of miR-182, PKR, and IFN-β are altered in RA and are significantly correlated with the osteoclastogenic capacity of RA monocytes. Our findings reveal a previously unrecognized regulatory network mediated by miR-182-PKR-IFN-β axis in osteoclastogenesis, and highlight the therapeutic implications of miR-182 inhibition in osteoprotection.

Indexed as

OsteogenesisAnimalsArthritis, RheumatoidAutocrine CommunicationBone ResorptioneIF-2 KinaseFemaleHomeostasisInterferon-betaMaleMice, Inbred C57BLMice, TransgenicMicroRNAsMonocyteseIF-2 KinaseInterferon-betaMicroRNAsMirn182 microRNA, mouse

Identifiers

PMID30291236
PMCPMC6173760
OpenAlexW2894989321

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.