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2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP)对大鼠前列腺的致癌性以及随后用丙酸睾酮治疗诱导浸润性癌

Carcinogenicity of 2-amino-1-methyl-6-phenylimidazo [4,5-b]pyridine (PhIP) in the rat prostate and induction of invasive carcinomas by subsequent treatment with testosterone propionate.

作者信息

Shirai T, Cui L, Takahashi S, Futakuchi M, Asamoto M, Kato K, Ito N

机构信息

First Department of Pathology, Nagoya City University Medical School, Nagoya, Japan.

出版信息

Cancer Lett. 1999 Sep 1;143(2):217-21. doi: 10.1016/s0304-3835(99)00128-7.

Abstract

2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) at 400 ppm in the diet for 52 weeks was found to induce non-invasive microscopic carcinomas in the ventral prostate of the treated rats, in addition to colon and mammary carcinomas. The current experimental data demonstrate that only a 20-week period of PhIP treatment is sufficient for induction of ventral carcinomas and that long-term pharmacological dosing with testosterone propionate which applied through a Silastic tube embedded in the subcutis after PhIP treatment can induce invasive carcinomas in the anterior prostate and seminal vesicles. Thus, PhIP may provide the basis for a good two stage carcinogenesis model for investigation of prostate carcinogenesis.

摘要

在饮食中添加400 ppm的2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP)持续52周,结果发现,除了诱发结肠癌和乳腺癌外,还会在接受治疗的大鼠腹侧前列腺中诱发非侵袭性微小癌。目前的实验数据表明,仅20周的PhIP治疗期就足以诱发腹侧癌,并且在PhIP治疗后通过皮下植入的硅橡胶管长期给予丙酸睾酮进行药物给药,可诱发前列腺前部和精囊的侵袭性癌。因此,PhIP可能为研究前列腺癌发生提供一个良好的两阶段致癌模型的基础。

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