| Literature DB >> 23651067 |
C K Martin1, W P Dirksen1, M M Carlton2, L G Lanigan1, S P Pillai1, J L Werbeck1, J K Simmons1, B E Hildreth1, C A London1, R E Toribio1, T J Rosol1.
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.Entities:
Keywords: bone invasion; bone resorption; feline; meloxicam; oral squamous cell carcinoma; zoledronic acid
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Year: 2013 PMID: 23651067 PMCID: PMC3751980 DOI: 10.1111/vco.12037
Source DB: PubMed Journal: Vet Comp Oncol ISSN: 1476-5810 Impact factor: 2.613