Study of feline oral squamous cell carcinoma:: Potential target for cyclooxygenase inhibitor treatment

被引:34
作者
DiBernardi, Lisa
Dore, Monique
Davis, John A.
Owens, Jane G.
Mohammed, Sulma I.
Guptill, Carolyn F.
Knapp, Deborah W. [1 ]
机构
[1] Purdue Univ, Sch Vet Med, Dept Vet Clin Sci, W Lafayette, IN 47907 USA
[2] Univ Montreal, Dept Pathol & Microbiol, Montreal, PQ, Canada
[3] Amgen Inc, Seattle, WA USA
[4] Elanco Anim Hlth, Greenfield, IN USA
[5] Purdue Univ, Dept Vet Pathobiol, W Lafayette, IN USA
[6] Purdue Univ, Purdue Canc Ctr, W Lafayette, IN USA
[7] Purdue Univ, Purdue Oncol Sci Ctr, W Lafayette, IN USA
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 2007年 / 76卷 / 04期
关键词
D O I
10.1016/j.plefa.2007.01.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oral squamous cell carcinoma (OSCC) is associated with high morbidity and mortality. A potential target for OSCC treatment is cyclooxygenase-2 (cox-2). Pet cats with naturally occurring OSCC may offer the opportunity to study anticancer activity of cox inhibitors. Cox-2 expression in feline OSCC was determined by immunohistochemistry. High intensity cox-2 immunoreactivity was detected in 6 of 34 (18%) feline OSCC samples. Weak immunoreactivity was noted in 22 OSCCs and in epithelial cells from oral mucosa of clinically normal cats. Pharmacokinetics of a cox inhibitor (piroxicam, 0.3 mg/kg) were studied in carcinoma-bearing cats to confirm a dose for follow-up trials. The average peak serum piroxicam concentration (948 ng/ml, which inhibited cox-2 activity) and serum half-life (15.9 h) were similar to that in normal cats. These results provide information (cox-2 expression as an inclusion criteria, 0.3 mg/kg daily piroxicam) for the design of follow-up trials of cox inhibitor treatment in pet cats with OSCC. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:245 / 250
页数:6
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