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选择性环氧化酶-2抑制剂尼美舒利和依托度酸对4-硝基喹啉1-氧化物诱发的大鼠舌鳞状细胞发育异常和癌的抑制作用。

Inhibitory effects of selective cyclooxygenase-2 inhibitors, nimesulide and etodolac, on the development of squamous cell dysplasias and carcinomas of the tongue in rats initiated with 4-nitroquinoline 1-oxide.

作者信息

Yamamoto Kazuhiko, Kitayama Wakashi, Denda Ayumi, Morisaki Ayumu, Kuniyasu Hiroki, Kirita Tadaaki

机构信息

Department of Oral and Maxillofacial Surgery, Nara Medical University, 840 Shijo-cho, Kashihara, Nara 634-8522, Japan.

出版信息

Cancer Lett. 2003 Sep 25;199(2):121-9. doi: 10.1016/s0304-3835(03)00382-3.

Abstract

The present study was conducted to examine the effects of selective cyclooxygenase (COX)-2 inhibitors, nimesulide and etodolac, on early stages of tongue carcinogenesis due to 4-nitroquinoline 1-oxide(4-NQO). Fischer 344 rats, 6 weeks old, were given 15 ppm of 4-NQO in their drinking water for 8 weeks followed by diet containing either nimesulide or etodolac at the doses of 150 and 300 ppm for 16 weeks. Rats were sacrificed at 24 weeks and tongue lesions were histologically examined. Nimesulide dose-dependently reduced the incidence and multiplicity of squamous cell dysplasias and carcinomas (SCCs), with significance at the 300 ppm dose. This suppression was associated with an increased incidence and multiplicity of hyperplasias. Etodolac exhibited similar but less extensive suppressive effects. The results suggest that COX-2 is involved in the progression of hyperplasia to dysplasia and from dysplasia to SCCs.

摘要

本研究旨在探讨选择性环氧化酶(COX)-2抑制剂尼美舒利和依托度酸对4-硝基喹啉1-氧化物(4-NQO)诱导的舌癌发生早期阶段的影响。6周龄的Fischer 344大鼠饮用含15 ppm 4-NQO的水8周,随后分别给予含150 ppm和300 ppm尼美舒利或依托度酸的饲料16周。在24周时处死大鼠,对舌部病变进行组织学检查。尼美舒利剂量依赖性地降低了鳞状细胞发育异常和癌(SCC)的发生率和多发性,在300 ppm剂量时具有显著性。这种抑制作用与增生的发生率和多发性增加有关。依托度酸表现出类似但程度较轻的抑制作用。结果表明,COX-2参与了从增生到发育异常以及从发育异常到SCC的进展过程。

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