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单次给予N-甲基-N-亚硝基脲诱导乳腺肿瘤的终生剂量-反应关系。

Lifetime dose-response relationships for mammary tumor induction by a single administration of N-methyl-N-nitrosourea.

作者信息

McCormick D L, Adamowski C B, Fiks A, Moon R C

出版信息

Cancer Res. 1981 May;41(5):1690-4.

PMID:7214338
Abstract

Dose-response relationships for the induction of mammary tumors by a single i.v. injection of N-methyl-N-nitrosourea (MNU) were studied. At 50 days of age, groups of 20 virgin female Sprague-Dawley rats received single doses of 50, 45, 40, 35, 30, 25, 20, 15, or 10 mg MNU per kg body weight; a group of 10 control rats received 0.85% NaCl solution only. Animals were observed for the appearance of mammary tumors over their life span or until 600 days after carcinogen administration. Both malignant and benign mammary tumors appeared in all groups; however, malignant tumors appeared earlier and at a faster rate than did benign tumors. Incidence of cancer and number of cancers per animal increased with increasing MNU dose; the latent period for cancer increased with decreasing dose. The number of benign tumors induced as a percentage of total tumors increased with decreasing dose, ranging from approximately 10% in groups receiving more than 30 mg MNU per kg to 58% in the group receiving 10 mg/kg. Foci of metastatic mammary carcinoma were found in lungs of animals in several MNU dose groups. Data from the present study indicate that a single i.v. administration of MNU induces mammary cancer in a dose-related fashion, with little toxicity and a short latent period; induced cancers metastasize to distant sites. The single-dose MNU model thus appears to be superior to both the 7,12-dimethylbenz(a)anthracene and multiple-dose MNU models, particularly for use in studies of modification of mammary carcinogenesis.

摘要

研究了单次静脉注射N-甲基-N-亚硝基脲(MNU)诱发乳腺肿瘤的剂量反应关系。50日龄时,将20只处女雌性斯普拉格-道利大鼠分为若干组,每组分别接受每千克体重50、45、40、35、30、25、20、15或10毫克MNU的单次剂量;一组10只对照大鼠仅接受0.85%氯化钠溶液。观察动物在其寿命期间或致癌剂给药后600天内乳腺肿瘤的出现情况。所有组均出现了恶性和良性乳腺肿瘤;然而,恶性肿瘤出现得更早,且比良性肿瘤的出现速度更快。癌症发病率和每只动物的癌症数量随MNU剂量增加而增加;癌症的潜伏期随剂量降低而增加。作为总肿瘤百分比诱导的良性肿瘤数量随剂量降低而增加,从每千克接受超过30毫克MNU的组中的约10%到接受10毫克/千克的组中的58%不等。在几个MNU剂量组动物的肺中发现了转移性乳腺癌灶。本研究数据表明,单次静脉注射MNU以剂量相关方式诱发乳腺癌,毒性小且潜伏期短;诱发的癌症转移至远处部位。因此,单剂量MNU模型似乎优于7,12-二甲基苯并(a)蒽和多剂量MNU模型,尤其适用于乳腺致癌作用修饰研究。

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