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通过激素替代对促性腺激素释放素类似物对7,12-二甲基苯并(a)蒽诱导的大鼠乳腺肿瘤的作用进行修饰。

Modification of the effect of a gonadoliberin analog on 7,12-dimethylbenz(a)anthracene-induced rat mammary tumors by hormone replacement.

作者信息

Rose D P, Pruitt B

出版信息

Cancer Res. 1979 Oct;39(10):3968-70.

PMID:113083
Abstract

A gonadoliberin analog, (D-leucyl6, desglycyl-NH2(10), prolyl ethylamide9) gonadoliberin, is known to suppress ovarian function and plasma prolactin levels. Its antitumor activity was evaluated against mammary tumors induced in Sprague-Dawley rats by dimethylbenz(a)anthracene. Observations were made when the analog, referred to as A-43818, was given alone and together with estrogen replacement or perphenazine, A-43818, 10 microgram s.c. twice a day for 6 weeks, was highly effective in producing tumor remissions. All of the 11 animals survived throughout the observation period, complete regressions occurred in 8 of 13 tumors, and 2 were classified as static. None of the 16 tumors in 12 control rats regressed, and there were 4 deaths. When estradiol benzoate, 2 microgram s.c. each day, was administered with the A-43818, antitumor activity was suppressed; only 2 of 17 tumors regressed, 6 were static, and 5 of the 10 rats in this group died. Perphenazine, 1 mg i.m. daily, a dose known to cause hyperprolactinemia, also impaired the efficacy of A-43818. Three of 14 tumors regressed, 6 were static, and the rest continued to grow; 3 of the 12 rats died within 6 weeks of starting treatment.

摘要

一种促性腺激素释放素类似物,即(D-亮氨酰6、去甘氨酰-NH2(10)、脯氨酰乙酰胺9)促性腺激素释放素,已知可抑制卵巢功能和血浆催乳素水平。对其抗二甲苯并(a)蒽诱导的斯普拉格-道利大鼠乳腺肿瘤的抗肿瘤活性进行了评估。观察了该类似物(称为A-43818)单独给药以及与雌激素替代物或奋乃静联合给药时的情况。A-43818,每天皮下注射10微克,共6周,在诱导肿瘤消退方面非常有效。11只动物在整个观察期内全部存活,13个肿瘤中有8个完全消退,2个被归类为静止状态。12只对照大鼠的16个肿瘤无一消退,且有4只死亡。当每天皮下注射2微克苯甲酸雌二醇并与A-43818联合给药时,抗肿瘤活性受到抑制;17个肿瘤中只有2个消退,6个静止,该组10只大鼠中有5只死亡。奋乃静,每天肌肉注射1毫克,已知该剂量会导致高催乳素血症,也会损害A-43818的疗效。14个肿瘤中有3个消退,6个静止,其余继续生长;12只大鼠中有3只在开始治疗的6周内死亡。

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