Evidence map›Paper›PMID 27567012›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2017

IL-36 Induces Bisphosphonate-Related Osteonecrosis of the Jaw-Like Lesions in Mice by Inhibiting TGF-β-Mediated Collagen Expression.

Sol Kim, Drake W Williams, Cindy Lee, Terresa Kim, Atsushi Arai, Songtao Shi, Xinmin Li, Ki-Hyuk Shin, Mo K Kang, No-Hee Park and 1 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04584840 (Conservative Versus Surgical Treatment for Medication Related Osteonecrosis of the Jaws), which is not on this map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 15% 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.

NCT04584840 naunknown statusnot on this mapstarted 2020, after this paper: background citation

Conservative Versus Surgical Treatment for Medication Related Osteonecrosis of the Jaws (MRONJ) Stages I and II, a Quasi-experimental Clinical Trial With Discovery of Salivary Biomarkers

TypeinterventionalSponsorFundació d'investigació Sanitària de les Illes BalearsRan2020 to 2024Enrolled50ConditionsOsteonecrosis of the Jaw, Bisphosphonate Induced, Osteonecrosis of the Jaw, Bisphosphonate RelatedArmsSurgical treatment
3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
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  10. Epithelial cells release IL-36α in extracellular vesicles following mechanical damage.Biochemical and biophysical research communications · 2022
    Article
  11. Review
  12. Article
  13. Frontiers in cellular and infection microbiology · 2022
    Article
  14. Review
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  16. Article
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  18. Review
  19. 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

11 authors at 5 institutions in 2 countries.

Sol KimThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA, USA.
Drake W WilliamsThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA, USA.
Cindy LeeThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA, USA.
Terresa KimThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA, USA.
Atsushi AraiThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA, USA.
Songtao ShiDepartment of Anatomy and Cell Biology, University of Pennsylvania, School of Medicine, Philadelphia, PA, USA.
Xinmin LiDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Ki-Hyuk ShinThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA, USA.
Mo K KangThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA, USA.
No-Hee ParkThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA, USA.
Reuben H KimThe Shapiro Family Laboratory of Viral Oncology and Aging Research, UCLA School of Dentistry, Los Angeles, CA, USA.
Institute of Aging · CAUCLA Jonsson Comprehensive Cancer CenterComprehensive Blood & Cancer Center · USUniversity of California, Los Angeles · USUniversity of Pennsylvania · US

Funding

Molecular mechanisms of drug-induced ONJ and osteomucosal chronic woundsR01DE023348 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KIM, REUBEN HAN-KYU · 2013 to 2017
$1.9M
Role of oral mucosa in bisphosphonate related osteonecrosis of the jawR03DE021114 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KIM, REUBEN HAN-KYU · 2010 to 2011
$231k
Role of pro-inflammatory cytokines in drug induced osteonecrosis of the jawF30DE025172 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WILLIAMS, DRAKE WINSLOW · 2015 to 2019
$220k
NIDCR NIH HHS F30 DE025172NIDCR NIH HHS R01 DE023348NIDCR NIH HHS R03 DE021114
6 · The paper itself

Abstract

Long-term administration of nitrogen-containing bisphosphonates can induce detrimental side effects such as bisphosphonate-related osteonecrosis of the jaw (BRONJ) in human. Although inflammation is known to be associated with BRONJ development, the detailed underlying mechanism remains unknown. Here, we report that the pro-inflammatory cytokine IL-36α is, in part, responsible for the BRONJ development. We found a notably higher level of IL-36α and lower level of collagen in the BRONJ lesions in mice. We also found that IL-36α remarkably suppressed TGF-β-mediated expression of Collα1 and α-Sma via the activation of Erk signaling pathway in mouse gingival mesenchymal stem cells. When IL-36 signaling was abrogated in vivo, development of BRONJ lesions was ameliorated in mice. Taken together, we showed the pathologic role of IL-36α in BRONJ development by inhibiting collagen expression and demonstrated that IL-36α could be a potential marker and a therapeutic target for the prevention and treatment of BRONJ. © 2016 American Society for Bone and Mineral Research.

Indexed as

AnimalsAntibodies, NeutralizingBisphosphonate-Associated Osteonecrosis of the JawCell NucleusCollagenExtracellular Signal-Regulated MAP KinasesFemaleGene Expression ProfilingInterleukin-1MAP Kinase Signaling SystemMice, Inbred C57BLModels, BiologicalPhosphorylationProtein TransportSmad ProteinsTransforming Growth Factor betaAntibodies, NeutralizingCollagenExtracellular Signal-Regulated MAP KinasesInterleukin-1Smad ProteinsTransforming Growth Factor betaBISPHOSPHONATECOLLAGENErkIL-36OSTEONECROSIS OF THE JAWTGF-β

Identifiers

PMID27567012
PMCPMC5642919
OpenAlexW2517857384

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.