Evidence map›Paper›PMID 30307042›Full record

ArticleVeterinary surgery : VS2018

Assessment of a novel nanoparticle hyperthermia therapy in a murine model of osteosarcoma.

Joanne L Tuohy, Jonathan E Fogle, Kristina Meichner, Luke B Borst, Christopher S Petty, Emily H Griffith, Jason A Osborne, B Duncan X Lascelles

Open access · greenAbstract read
In one paragraph

Article in Veterinary surgery : VS, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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.

Joanne L TuohyDepartment of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina.
Jonathan E FogleDepartment of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina.ORCID http://orcid.org/0000-0003-3837-6719
Kristina MeichnerDepartment of Pathology, College of Veterinary Medicine, University of Georgia, Athens, Georgia.
Luke B BorstDepartment of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina.
Christopher S PettyKaio Therapy, Raleigh, North Carolina.
Emily H GriffithDepartment of Statistics, College of Sciences, North Carolina State University, Raleigh, North Carolina.
Jason A OsborneDepartment of Statistics, College of Sciences, North Carolina State University, Raleigh, North Carolina.
B Duncan X LascellesDepartment of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina.
North Carolina State University · USKaio Therapy (United States) · USUniversity of Georgia · US

Funding

Comparative Medicine and Translational Research Training ProgramT32OD011130 · OD · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Lauren Virginia Schnabel · 2012 to 2026
$7.8M
NIH HHS T32 OD011130
6 · The paper itself

Abstract

objectiveTo evaluate the effects of nanoparticle hyperthermia therapy on monocyte function and tumor-derived factors associated with macrophage polarization in a murine osteosarcoma model. STUDY

designExperimental study. ANIMALS: Female C3H mice.

methodsPeripheral blood monocyte cell surface phenotype, monocyte chemotaxis, tumor messenger RNA expression, and survival were compared among osteosarcoma (OS)-bearing mice treated with nanoparticle hyperthermia therapy, OS-bearing mice with osteomyelitis, OS-bearing mice, vehicle control mice, and normal control mice.

resultsOS-bearing mice with osteomyelitis had a higher proportion of "nonclassical" monocytes (Ly6C

conclusionOS likely induced alterations in monocyte phenotype and function. Nanoparticle hyperthermia therapy increased in vitro monocyte chemotaxis. CLINICAL IMPACT: Enhancing monocyte/macrophage function in dogs with OS may enhance antitumor immunity.

Indexed as

NanoparticlesAnimalsBone NeoplasmsDisease Models, AnimalDog DiseasesDogsFemaleHyperthermia, InducedMiceMice, Inbred C3HMonocytesOsteosarcomaPhenotypeReceptors, CXCR4CXCR4 protein, humanReceptors, CXCR4

Identifiers

PMID30307042
PMCPMC7362588
OpenAlexW2895992052

What OpenQuestion holds

Textmetadata
LicenceTDM
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.