Evidence map›Paper›PMID 37350025›Full record

ArticleJournal of dental research2023

Inhibition of Mertk Signaling Enhances Bone Healing after Tooth Extraction.

A M Decker, M Matsumoto, J T Decker, A Roh, N Inohara, J Sugai, K Martin, R Taichman, D Kaigler, L D Shea and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of dental research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. The Role of TAM Receptors in Bone.International journal of molecular sciences · 2023
    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

11 authors at 2 institutions in 1 country.

A M DeckerDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.
M MatsumotoDepartment of Pathology, School of Medicine, University of Michigan, Ann Arbor, MI, USA.
J T DeckerDepartment of Cariology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.
A RohDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.
N InoharaDepartment of Pathology, School of Medicine, University of Michigan, Ann Arbor, MI, USA.
J SugaiDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.
K MartinDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.
R TaichmanSchool of Dentistry, University of Alabama-Birmingham, Birmingham, AL, USA.
D KaiglerDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.
L D SheaDepartment of Biomedical Engineering, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.
G NúñezDepartment of Pathology, School of Medicine, University of Michigan, Ann Arbor, MI, USA.
University of Michigan–Ann Arbor · USUniversity of Alabama at Birmingham · US

Funding

Tumor microvesicle-mediated modulation of the bone microenvironmentP01CA093900 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KELLER, EVAN T · 2004 to 2024
$29.6M
Structure, Composition, & Histology Core - Core BP30AR069620 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KARL J JEPSEN · 2016 to 2026
$8.4M
Redefining mesenchymal stem cells: using their cellular and molecular phenotypes to determine their regenerative and therapeutic propertiesR01DE028657 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KAIGLER, DARNELL · 2019 to 2023
$2.1M
GAS6-mediated alveolar bone regeneration - Admin SupplementR00DE029756 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DECKER, ANN MARIE · 2022 to 2024
$842k
GAS6-Mediated Regulation of Oral Tissue RegenerationK99DE029756 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DECKER, ANN MARIE · 2020 to 2021
$279k
NCI NIH HHS P01 CA093900NIAMS NIH HHS P30 AR069620NIDCR NIH HHS K99 DE029756NIDCR NIH HHS L30 DE029054NIDCR NIH HHS R00 DE029756NIDCR NIH HHS R01 DE028657
6 · The paper itself

Abstract

Regeneration of alveolar bone is an essential step in restoring healthy function following tooth extraction. Growth of new bone in the healing extraction socket can be variable and often unpredictable when systemic comorbidities are present, leading to the need for additional therapeutic targets to accelerate the regenerative process. One such target is the TAM family (Tyro3, Axl, Mertk) of receptor tyrosine kinases. These proteins have been shown to help resolve inflammation and maintain bone homeostasis and thus may have therapeutic benefits in bone regeneration following extraction. Treatment of mice with a pan-TAM inhibitor (RXDX-106) led to accelerated alveolar bone fill following first molar extraction in a mouse model without changing immune infiltrate. Treatment of human alveolar bone mesenchymal stem cells with RXDX-106 upregulated Wnt signaling and primed the cells for osteogenic differentiation. Differentiation of human alveolar bone mesenchymal stem cells with osteogenic media and TAM-targeted inhibitor RXDX-106 (pan-TAM), ASP-2215 (Axl specific), or MRX-2843 (Mertk specific) showed enhanced mineralization with pan-TAM or Mertk-specific inhibitors and no change with Axl-specific inhibitor. First molar extractions in Mertk

Indexed as

Axl Receptor Tyrosine KinaseProto-Oncogene ProteinsAnimalsc-Mer Tyrosine KinaseHumansMiceOsteogenesisTooth ExtractionTooth SocketAxl Receptor Tyrosine Kinasec-Mer Tyrosine KinaseMertk protein, mouseProto-Oncogene ProteinsinflammationosteoblastsosteogenesisRXDX-106wound healing

Identifiers

PMID37350025
PMCPMC10552464
OpenAlexW4381714952

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.