Evidence map›Paper›PMID 30813941›Full record

ArticleJournal of translational medicine2019

Jaw osteosarcoma models in mice: first description.

Hélios Bertin, Romain Guilho, Régis Brion, Jérôme Amiaud, Séverine Battaglia, Anne Moreau, Anne Brouchet-Gomez, Julie Longis, Benoit Piot, Dominique Heymann and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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

12 authors at 5 institutions in 2 countries.

Hélios BertinLaboratoire des sarcomes osseux et remodelage des tissus calcifiés (Phy.OS), UMR 1238, Faculté de médecine, 1 rue Gaston Veil, 44035, Nantes Cedex, France. helios.bertin@chu-nantes.fr.
Romain GuilhoFaculty of Population Health Sciences, UCL Institute of Child Health, 30 Guilford Street, London, England, WC1N 1EH, UK.
Régis BrionLaboratoire des sarcomes osseux et remodelage des tissus calcifiés (Phy.OS), UMR 1238, Faculté de médecine, 1 rue Gaston Veil, 44035, Nantes Cedex, France.
Jérôme AmiaudLaboratoire des sarcomes osseux et remodelage des tissus calcifiés (Phy.OS), UMR 1238, Faculté de médecine, 1 rue Gaston Veil, 44035, Nantes Cedex, France.
Séverine BattagliaLaboratoire des sarcomes osseux et remodelage des tissus calcifiés (Phy.OS), UMR 1238, Faculté de médecine, 1 rue Gaston Veil, 44035, Nantes Cedex, France.
Anne MoreauService d'anatomie et cytologie pathologique, CHU de Nantes, 1 place Alexis Ricordeau, 44093, Nantes Cedex 1, France.
Anne Brouchet-GomezService d'anatomie et cytologie pathologique, Institut Universitaire du Cancer Toulouse Oncopôle, 1 avenue Irène Joliot-Curie, 31059, Toulouse Cedex 9, France.
Julie LongisService de chirurgie Maxillo-faciale et stomatologie, CHU de Nantes, 1 place Alexis Ricordeau, 44093, Nantes Cedex 1, France.
Benoit PiotService de chirurgie Maxillo-faciale et stomatologie, CHU de Nantes, 1 place Alexis Ricordeau, 44093, Nantes Cedex 1, France.
Dominique HeymannLaboratoire Hétérogénéité Tumorale et Médecine de Précision, Institut de Cancérologie de l'Ouest, Boulevard Jacques Monod, 44805, Saint Herblain, France.
Pierre CorreService de chirurgie Maxillo-faciale et stomatologie, CHU de Nantes, 1 place Alexis Ricordeau, 44093, Nantes Cedex 1, France.
Françoise RédiniLaboratoire des sarcomes osseux et remodelage des tissus calcifiés (Phy.OS), UMR 1238, Faculté de médecine, 1 rue Gaston Veil, 44035, Nantes Cedex, France.
Centre Hospitalier Universitaire de Nantes · FRInstitut de Cancérologie de l'Ouest · FRInstitut universitaire du cancer de Toulouse Oncopole · FRLe Laboratoire d'Ingénierie Ostéo-Articulaire et Dentaire · FRUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteosarcoma (OS) is the most common cancer of bone. Jaw osteosarcoma (JOS) is rare and it differs from other OS in terms of the time of occurrence (two decades later) and better survival. The aim of our work was to develop and characterize specific mouse models of JOS.

methodsSyngenic and xenogenic models of JOS were developed in mice using mouse (MOS-J) and human (HOS1544) osteosarcoma cell lines, respectively. An orthotopic patient-derived xenograft model (PDX) was also developed from a mandibular biopsy. These models were characterized at the histological and micro-CT imaging levels, as well as in terms of tumor growth and metastatic spread.

resultsHomogeneous tumor growth was observed in both the HOS1544 and the MOS-J JOS models by injection of 0.25 × 10

conclusionWe describe the first animal model of JOS and its potential use for therapeutic applications. This model needs to be compared with the usual long-bone osteosarcoma models to investigate potential differences in the bone microenvironment.

Indexed as

Xenograft Model Antitumor AssaysAnimalsCell Line, TumorCell ProliferationFemaleHumansJaw NeoplasmsLung NeoplasmsMandibleMice, Inbred C57BLMice, SCIDOsteosarcomaTumor BurdenX-Ray MicrotomographyAnimal experimentationBone resorptionEnvironmentMandibleModelsSarcoma

Identifiers

PMID30813941
PMCPMC6391788
OpenAlexW2931871459

What OpenQuestion holds

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LicenceCC BY
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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.