首页> 外文期刊>Prostaglandins, Leukotrienes, and Essential Fatty Acids >Pretreatment tumor prostaglandin E2 concentration and cyclooxygenase-2 expression are not associated with the response of canine naturally occurring invasive urinary bladder cancer to cyclooxygenase inhibitor therapy.
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Pretreatment tumor prostaglandin E2 concentration and cyclooxygenase-2 expression are not associated with the response of canine naturally occurring invasive urinary bladder cancer to cyclooxygenase inhibitor therapy.

机译:预处理肿瘤前列腺素E2浓度和环氧合酶2表达与犬自然发生的浸润性膀胱癌对环氧合酶抑制剂治疗的反应无关。

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摘要

The purpose of this study was to determine the extent to which pretreatment prostaglandin E2 (PGE2) concentration and cyclooxygenase-2 (cox-2) expression could be used to predict the antitumor activity of cox inhibitor treatment in naturally occurring canine transitional cell carcinoma of the urinary bladder (TCC). Snap frozen tissues (to measure PGE2) and formalin-fixed TCC samples (for cox-2 immunohistochemistry) were obtained by cystoscopy or surgery. Complete tumor staging was performed before and after one month of treatment with the cox inhibitor, piroxicam (0.3 mg/kg q24 h po). The pretreatment PGE2 concentration ranged from 57 to 1624 ng/g of TCC tissue; n=18 dogs). Cox-2 immunoreactivity was observed in all TCC samples. There was no association between PGE2 concentration, cox-2 expression, and change in tumor volume with piroxicam treatment. In conclusion, cox-2 expression or PGE2 concentration alone, or the combination of the two was not useful in predicting response to piroxicam treatment incanine TCC.
机译:本研究的目的是确定预处理前列腺素E2(PGE2)的浓度和环氧合酶2(cox-2)的表达可用于预测Cox抑制剂治疗天然存在的犬转化性肝癌的抗肿瘤活性的程度。膀胱(TCC)。通过膀胱镜或手术获得速冻组织(用于测量PGE2)和福尔马林固定的TCC样品(用于cox-2免疫组织化学)。在用cox抑制剂吡罗昔康(0.3 mg / kg,每24小时口服一次)治疗一个月之前和之后,进行了完整的肿瘤分期。预处理PGE2的TCC组织浓度为57至1624 ng / g。 n = 18条狗)。在所有TCC样品中均观察到Cox-2免疫反应性。在吡罗昔康治疗下,PGE2浓度,cox-2表达和肿瘤体积变化之间没有关联。总之,单独的cox-2表达或PGE2浓度,或两者的组合在预测吡罗昔康治疗犬TCC的反应中无用。

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