Evidence map›Paper›PMID 24607847›Full record

ArticleJournal of dentistry2014

Extracts of irradiated mature human tooth crowns contain MMP-20 protein and activity.

J D McGuire, A A Mousa, Bo J Zhang, L S Todoki, N T Huffman, K B Chandrababu, J Moradian-Oldak, A Keightley, Y Wang, M P Walker and 1 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of dentistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Microshear bond strength of conventional and bioactive restorative materials to irradiated and non-irradiated dentin: an in vitro study.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
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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 2 institutions in 1 country.

J D McGuireDepartment of Oral and Craniofacial Science, Center of Excellence in Dental and Musculoskeletal Tissues, School of Dentistry, University of Missouri-Kansas City, Kansas City, MO, United States.
A A MousaDepartment of Oral and Craniofacial Science, Center of Excellence in Dental and Musculoskeletal Tissues, School of Dentistry, University of Missouri-Kansas City, Kansas City, MO, United States.
Bo J ZhangDepartment of Oral and Craniofacial Science, Center of Excellence in Dental and Musculoskeletal Tissues, School of Dentistry, University of Missouri-Kansas City, Kansas City, MO, United States.
L S TodokiDepartment of Oral and Craniofacial Science, Center of Excellence in Dental and Musculoskeletal Tissues, School of Dentistry, University of Missouri-Kansas City, Kansas City, MO, United States.
N T HuffmanDepartment of Oral and Craniofacial Science, Center of Excellence in Dental and Musculoskeletal Tissues, School of Dentistry, University of Missouri-Kansas City, Kansas City, MO, United States.
K B ChandrababuCenter for Craniofacial Molecular Biology, Ostrow School of Dentistry, University of Southern California, Los Angeles, CA, United States.
J Moradian-OldakCenter for Craniofacial Molecular Biology, Ostrow School of Dentistry, University of Southern California, Los Angeles, CA, United States.
A KeightleyBiological Mass Spectrometry and Proteomics Facility, School of Biological Sciences, University of Missouri-Kansas City, MO, United States.
Y WangDepartment of Oral and Craniofacial Science, Center of Excellence in Dental and Musculoskeletal Tissues, School of Dentistry, University of Missouri-Kansas City, Kansas City, MO, United States.
M P WalkerDepartment of Oral and Craniofacial Science, Center of Excellence in Dental and Musculoskeletal Tissues, School of Dentistry, University of Missouri-Kansas City, Kansas City, MO, United States.
J P GorskiDepartment of Oral and Craniofacial Science, Center of Excellence in Dental and Musculoskeletal Tissues, School of Dentistry, University of Missouri-Kansas City, Kansas City, MO, United States. Electronic address: gorskij@umkc.edu.
University of Missouri–Kansas City · USUniversity of Southern California · US

Funding

MATRIX-BASED MINERAL (MBM) ENAMEL BIOMIMETICSR01DE013414 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Janet Oldak · 2001 to 2026
$8.6M
INTRINSICALLY DISORDERED PROTEINS IN BIOMINERALIZATIONR01DE020099 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI OLDAK, JANET · 2009 to 2013
$2.0M
Understanding the mechanism of radiotherapy-induced dentition breakdownR01DE021462 · NIDCR · UNIVERSITY OF MISSOURI KANSAS CITY · PI WALKER, MARY P, WANG, YONG · 2010 to 2014
$1.8M
Zeiss LSM 710 Confocal Microscopy System for Imaging of Mineralized TissuesS10RR027668 · NCRR · UNIVERSITY OF MISSOURI KANSAS CITY · PI DALLAS, SARAH L · 2011 to 2011
$446k
NCRR NIH HHS S10 RR027668NCRR NIH HHS S10RR027668NIDCR NIH HHS R01 DE013414NIDCR NIH HHS R01 DE020099NIDCR NIH HHS R01 DE021462
6 · The paper itself

Abstract

objectivesWe recently demonstrated a significant correlation between enamel delamination and tooth-level radiation dose in oral cancer patients. Since radiation can induce the synthesis and activation of matrix metalloproteinases, we hypothesized that irradiated teeth may contain active matrix metalloproteinases. MATERIALS AND

methodsExtracted teeth from oral cancer patients treated with radiotherapy and from healthy subjects were compared. Extracted mature third molars from healthy subjects were irradiated in vitro and/or incubated for 0-6 months at 37°C. All teeth were then pulverized, extracted, and extracts subjected to proteomic and enzymatic analyses.

resultsScreening of irradiated crown extracts using mass spectrometry identified MMP-20 (enamelysin) which is expressed developmentally in dentine and enamel but believed to be removed prior to tooth eruption. MMP-20 was composed of catalytically active forms at Mr=43, 41, 24 and 22kDa and was immunolocalized predominantly to the morphological dentine enamel junction. The proportion of different sized MMP-20 forms changed with incubation and irradiation. While the pattern was not altered directly by irradiation of healthy teeth with 70Gy, subsequent incubation at 37°C for 3-6 months with or without prior irradiation caused the proportion of Mr=24-22kDa MMP-20 bands to increase dramatically. Extracts of teeth from oral cancer patients who received >70Gy radiation also contained relatively more 24 and 22kDa MMP-20 than those of healthy age-related teeth.

conclusionMMP-20 is a radiation-resistant component of mature tooth crowns enriched in the dentine-enamel. We speculate that MMP-20 catalyzed degradation of organic matrix at this site could lead to enamel delamination associated with oral cancer radiotherapy.

Indexed as

AgedBlotting, WesternDental EnamelDentinElectrophoresisHumansMass SpectrometryMatrix Metalloproteinase 20Microscopy, ConfocalMiddle AgedMolar, ThirdRadiotherapy DosageTandem Mass SpectrometryTooth CrownYoung AdultMatrix Metalloproteinase 20MMP20 protein, humanDentine–enamel junctionHuman tooth crownMatrix metalloproteinase-20Oral cancerRadiotherapy

Identifiers

PMID24607847
PMCPMC4326248
OpenAlexW2002441345

What OpenQuestion holds

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LicenceTDM
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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.