Evidence map›Paper›PMID 23651067›Full record

ArticleVeterinary and comparative oncology2015

Combined zoledronic acid and meloxicam reduced bone loss and tumour growth in an orthotopic mouse model of bone-invasive oral squamous cell carcinoma.

C K Martin, W P Dirksen, M M Carlton, L G Lanigan, S P Pillai, J L Werbeck, J K Simmons, B E Hildreth, C A London, R E Toribio and 1 more

Open access · greenAbstract read
In one paragraph

Article in Veterinary and comparative oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  8. Cats, Cancer and Comparative Oncology.Veterinary sciences · 2015
    Review
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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 1 institution in 1 country.

C K MartinDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
W P DirksenDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
M M CarltonSmall Animal Imaging Center Shared Resource, Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.
L G LaniganDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
S P PillaiDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
J L WerbeckDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
J K SimmonsDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
B E HildrethDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
C A LondonDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
R E ToribioDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
T J RosolDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
Imaging Center · US

Funding

Mechanisms of bone invasion and tumor growth in models of head and neck cancer.F32CA130458 · NCI · OHIO STATE UNIVERSITY · PI MARTIN, CHELSEA · 2007 to 2009
$191k
NCI NIH HHS F32 CA130458
6 · The paper itself

Abstract

Oral squamous cell carcinoma (OSCC) is common in cats and humans and invades oral bone. We hypothesized that the cyclooxygenase (COX)-2 inhibitor, meloxicam, with the bisphosphonate, zoledronic acid (ZOL), would inhibit tumour growth, osteolysis and invasion in feline OSCC xenografts in mice. Human and feline OSCC cell lines expressed COX-1 and COX-2 and the SCCF2 cells had increased COX-2 mRNA expression with bone conditioned medium. Luciferase-expressing feline SCCF2Luc cells were injected beneath the perimaxillary gingiva and mice were treated with 0.1 mg kg(-1) ZOL twice weekly, 0.3 mg kg(-1) meloxicam daily, combined ZOL and meloxicam, or vehicle. ZOL inhibited osteoclastic bone resorption at the tumour-bone interface. Meloxicam was more effective than ZOL at reducing xenograft growth but did not affect osteoclastic bone resorption. Although a synergistic effect of combined ZOL and meloxicam was not observed, combination therapy was well-tolerated and may be useful in the clinical management of bone-invasive feline OSCC.

Indexed as

Analysis of VarianceAnimalsAntineoplastic Combined Chemotherapy ProtocolsBone Density Conservation AgentsBone NeoplasmsBone ResorptionCat DiseasesCatsCell Line, TumorCyclooxygenase 1Cyclooxygenase 2Cyclooxygenase InhibitorsDiphosphonatesDisease Models, AnimalHeterograftsHumansBone Density Conservation AgentsCyclooxygenase 1Cyclooxygenase 2Cyclooxygenase InhibitorsDiphosphonatesImidazolesMeloxicamPTGS1 protein, humanPTGS2 protein, humanRNA, MessengerThiazinesThiazolesZoledronic Acidbone invasionbone resorptionfelinemeloxicamoral squamous cell carcinomazoledronic acid

Identifiers

PMID23651067
PMCPMC3751980
OpenAlexW1496109623

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.