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经胎盘致癌作用研究的一些结果与展望。

Some results and prospects of transplacental carcinogenesis studies.

作者信息

Alexandrov V A

出版信息

Neoplasma. 1976;23(3):285-99.

PMID:822360
Abstract

Analysis of literary data and the author's findings have shown that the transplacental action of most of the compounds tested in experiments on rats manifested itself by a neurotropic carcinogenic effect. A marked neurotropism in transplacental carcinogenesis in rats is characteristic even for such drugs (e.g. dimethylbenzathracene) that have never induced neurogenic neoplasms in adult animals. To elucidate the relationship between teratogenesis and carcinogenesis the peculiarities of tumor development in brain against the background of malformations induced by combined transplacental treatment by methylnitrosourea (MNU) and ethylnitrosourea (ENU) in rats have been studied. Tumorigenesis was sharply inhibited by administration of ENU (on the 13th day) prior to MNU treatment (on the 15th day). There is reason to believe that the cytotoxic effect of MNU for microephaly results in the death of a considerable part of the cell population already transformed by ENU. In a special series of experiments characteristics of the permeability of polycyclic aromatic hydrocarbons through the placenta in rats have been specified.

摘要

对文献数据的分析以及作者的研究结果表明,在大鼠实验中所测试的大多数化合物的经胎盘作用表现为一种嗜神经致癌效应。即使对于那些在成年动物中从未诱发过神经源性肿瘤的药物(如二甲基苯并蒽),大鼠经胎盘致癌过程中显著的嗜神经性也是其特征之一。为了阐明致畸作用与致癌作用之间的关系,研究了在大鼠中经胎盘联合给予甲基亚硝基脲(MNU)和乙基亚硝基脲(ENU)所诱发畸形的背景下,脑肿瘤发生的特点。在MNU处理(第15天)之前给予ENU(第13天)可显著抑制肿瘤发生。有理由相信,MNU对小头畸形的细胞毒性作用导致了相当一部分已被ENU转化的细胞群体死亡。在一系列特殊实验中,已经明确了多环芳烃在大鼠胎盘的通透性特征。

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