Evidence map›Paper›PMID 32290096›Full record

ArticleInternational journal of molecular sciences2020

Underlying Ossification Phenotype in a Murine Model of Metastatic Synovial Sarcoma.

Matthew Kirkham, Austen Kalivas, Kaniz Fatema, Sarah Luelling, Brooke H Dubansky, Benjamin Dubansky, Kevin B Jones, Jared J Barrott

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 3 institutions in 1 country.

Matthew KirkhamDepartment of Biomedical and Pharmaceutical Sciences, Idaho State University, Pocatello, ID 83201, USA.
Austen KalivasDepartment of Biomedical and Pharmaceutical Sciences, Idaho State University, Pocatello, ID 83201, USA.
Kaniz FatemaDepartment of Biomedical and Pharmaceutical Sciences, Idaho State University, Pocatello, ID 83201, USA.
Sarah LuellingDepartment of Biomedical and Pharmaceutical Sciences, Idaho State University, Pocatello, ID 83201, USA.
Brooke H DubanskyDepartment of Medical Laboratory Sciences & Public Health, Tarleton State University, Fort Worth, TX 76104, USA.
Benjamin DubanskyDepartment of Biological Sciences, University of North Texas, Denton, TX 76203, USA.
Kevin B JonesDepartments of Orthopaedics and Oncological Sciences, Huntsman Cancer Institute, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
Jared J BarrottDepartment of Biomedical and Pharmaceutical Sciences, Idaho State University, Pocatello, ID 83201, USA.ORCID 0000-0001-6059-9009
Idaho State University · USUniversity of North Texas · USUniversity of Utah · US

Funding

Women's health: interplay of maternal diet and key demographics on neurological health in the rural frontier and remote WestP20GM103408 · NIGMS · UNIVERSITY OF IDAHO · PI Scott A Minnich · 2012 to 2026
$59.8M
Targeting SS18-SSX biology in synovial sarcomagenesisU54CA231652 · NCI · UNIVERSITY OF UTAH · PI JONES, KEVIN BRUCE · 2018 to 2022
$12.0M
Epigenetic Mechanisms Driving Synovial SarcomagenesisR01CA201396 · NCI · UNIVERSITY OF UTAH · PI CAIRNS, BRADLEY R., JONES, KEVIN BRUCE · 2017 to 2021
$1.7M
CSRD VA 1NCI NIH HHS R01 CA201396NCI NIH HHS R01CA201396NCI NIH HHS U54 CA231652NIGMS NIH HHS P20 GM103408
6 · The paper itself

Abstract

Synovial sarcoma, an uncommon cancer, typically affects young adults. Survival rates range from 36% to 76%, decreasing significantly when metastases are present. Synovial sarcomas form in soft tissues, often near bones, with about 10% demonstrating ossification in the tumor. The literature is inconclusive on whether the presence of ossification portends a worse prognosis. To this end, we analyzed our genetic mouse models of synovial sarcoma to determine the extent of ossification in the tumors and its relationship with morbidity. We noted higher ossification within our metastatic mouse model of synovial sarcoma. Not only did we observe ossification within the tumors at a frequency of 7%, but an even higher frequency, 72%, of bone reactivity was detected by radiography. An enrichment of bone development genes was associated with primary tumors, even in the absence of an ossification phenotype. In spite of the ossification being intricately linked with the metastatic model, the presence of ossification was not associated with a faster or worse morbidity in the mice. Our conclusion is that both metastasis and ossification are dependent on time, but that they are independent of one another.

Indexed as

Ossification, HeterotopicPhenotypeAnimalsBiomarkers, TumorBiopsyBone and BonesDisease Models, AnimalGene Expression ProfilingGene FusionGenotypeHumansImmunohistochemistryKaplan-Meier EstimateMiceNeoplasm MetastasisPrognosisBiomarkers, Tumorbone development genesheterotopic ossificationinflammationintralesional calcificationmetastasisparathyroid hormone-like hormonesynovial sarcoma

Identifiers

PMID32290096
PMCPMC7177647
OpenAlexW3016126665

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.