Evidence map›Paper›PMID 26107959›Full record

ArticlePloS one2015

The identification of proteoglycans and glycosaminoglycans in archaeological human bones and teeth.

Yvette M Coulson-Thomas, Vivien J Coulson-Thomas, Andrew L Norton, Tarsis F Gesteira, Renan P Cavalheiro, Maria Cecília Z Meneghetti, João R Martins, Ronald A Dixon, Helena B Nader

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 45 citations in OpenAlex.

  1. Potential Targeting Mechanisms for Bone-Directed Therapies.International journal of molecular sciences · 2024
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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

9 authors at 4 institutions in 3 countries.

Yvette M Coulson-ThomasDepartment of Biochemistry, Universidade Federal de São Paulo, São Paulo, Brazil; School of Life Sciences, University of Lincoln, Lincoln, Lincs, United Kingdom.
Vivien J Coulson-ThomasDepartment of Biochemistry, Universidade Federal de São Paulo, São Paulo, Brazil; Department of Ophthalmology, College of Medicine, Edith J. Crawley Vision Research Center, University of Cincinnati, Cincinnati, Ohio, United States of America.
Andrew L NortonDurham University, Durham, United Kingdom.
Tarsis F GesteiraDepartment of Biochemistry, Universidade Federal de São Paulo, São Paulo, Brazil; Department of Ophthalmology, College of Medicine, Edith J. Crawley Vision Research Center, University of Cincinnati, Cincinnati, Ohio, United States of America.
Renan P CavalheiroDepartment of Biochemistry, Universidade Federal de São Paulo, São Paulo, Brazil.
Maria Cecília Z MeneghettiDepartment of Biochemistry, Universidade Federal de São Paulo, São Paulo, Brazil.
João R MartinsDepartment of Biochemistry, Universidade Federal de São Paulo, São Paulo, Brazil.
Ronald A DixonSchool of Life Sciences, University of Lincoln, Lincoln, Lincs, United Kingdom.
Helena B NaderDepartment of Biochemistry, Universidade Federal de São Paulo, São Paulo, Brazil.
Universidade Federal de São Paulo · BRUniversity of Lincoln · GBDurham University · GBUniversity of Cincinnati · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone tissue is mineralized dense connective tissue consisting mainly of a mineral component (hydroxyapatite) and an organic matrix comprised of collagens, non-collagenous proteins and proteoglycans (PGs). Extracellular matrix proteins and PGs bind tightly to hydroxyapatite which would protect these molecules from the destructive effects of temperature and chemical agents after death. DNA and proteins have been successfully extracted from archaeological skeletons from which valuable information has been obtained; however, to date neither PGs nor glycosaminoglycan (GAG) chains have been studied in archaeological skeletons. PGs and GAGs play a major role in bone morphogenesis, homeostasis and degenerative bone disease. The ability to isolate and characterize PG and GAG content from archaeological skeletons would unveil valuable paleontological information. We therefore optimized methods for the extraction of both PGs and GAGs from archaeological human skeletons. PGs and GAGs were successfully extracted from both archaeological human bones and teeth, and characterized by their electrophoretic mobility in agarose gel, degradation by specific enzymes and HPLC. The GAG populations isolated were chondroitin sulfate (CS) and hyaluronic acid (HA). In addition, a CSPG was detected. The localization of CS, HA, three small leucine rich PGs (biglycan, decorin and fibromodulin) and glypican was analyzed in archaeological human bone slices. Staining patterns were different for juvenile and adult bones, whilst adolescent bones had a similar staining pattern to adult bones. The finding that significant quantities of PGs and GAGs persist in archaeological bones and teeth opens novel venues for the field of Paleontology.

Indexed as

ArchaeologyBone and BonesGlycosaminoglycansHumansProteoglycansToothGlycosaminoglycansProteoglycans

Identifiers

PMID26107959
PMCPMC4481269
OpenAlexW1880522608

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.