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7,12-二甲基苯并[a]蒽与大鼠乳腺DNA结合的年龄相关性改变。

Age-related modification of 7,12-dimethylbenz[a]anthracene binding to rat mammary gland DNA.

作者信息

Janss D H, Ben T L

出版信息

J Natl Cancer Inst. 1978 Jan;60(1):173-7. doi: 10.1093/jnci/60.1.173.

Abstract

The binding of 7,12-dimethylbenz[a]anthracene (DMBA) to mammary gland and liver DNA of female Sprague-Dawley rats either 35, 50, or 120 days of age at the time of carcinogen administration was studied. Following a single oral feeding of tritium-labeled DMBA, the level of binding to liver DNA of rats in all 3 age groups was significantly lower, at all times during a 6-week period, than that of binding to mammary DNA. The amount of DMBA bound to liver DNA was a function of the amount of carcinogen administered and not the age of the animal. In contrast, DMBA binding to mammary DNA was dependent on the age of the animal at the time of carcinogen feeding. Furthermore, in the age group with 100% tumor induction (50 days old), DMBA binding increased directly with the amount of carcinogen fed; this was not the case for the other 2 age groups. These results indicated that a significant correlation existed between the age of the rat, the amount of DMBA bound to DNA, and the incidence of mammary tumors following carcinogen feeding.

摘要

研究了在给予致癌物时,7,12 - 二甲基苯并[a]蒽(DMBA)与35日龄、50日龄或120日龄雌性斯普拉格 - 道利大鼠乳腺和肝脏DNA的结合情况。在单次口服给予氚标记的DMBA后,在6周期间的所有时间,所有3个年龄组大鼠肝脏DNA的结合水平均显著低于乳腺DNA的结合水平。与肝脏DNA结合的DMBA量是给予致癌物量的函数,而不是动物年龄的函数。相比之下,DMBA与乳腺DNA的结合取决于给予致癌物时动物的年龄。此外,在肿瘤诱导率为100%的年龄组(50日龄)中,DMBA结合量随给予的致癌物量直接增加;其他2个年龄组则并非如此。这些结果表明,大鼠年龄、与DNA结合的DMBA量以及给予致癌物后乳腺肿瘤的发生率之间存在显著相关性。

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