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炔诺酮分散了石川细胞中经银染的核仁组织区。

Norethindrone scatters silver-stained nucleolar organizer regions of Ishikawa cells.

作者信息

Yokoyama Y, Niwa K, Tamaya T

机构信息

Department of Obstetrics and Gynecology, Gifu University School of Medicine, Japan.

出版信息

Cancer Res. 1991 Nov 1;51(21):5987-92.

PMID:1718592
Abstract

We investigated the effects of sex steroids on silver-stained nucleolar organizer regions (Ag-NORs) and DNA/RNA kinetics in Ishikawa cells. Norethindrone and its isomer norethynodrel exclusively caused Ag-NORs to scatter in the nuclear matrix, from the nucleolus. No such effect occurred with the other sex steroids tested, including progestational, androgenic, and estrogenic compounds. Nuclear argyrophilic substances induced by norethindrone, as well as nucleolar ones, were neither DNA nor RNA but protein. Electron microscopy showed that norethindrone caused nucleolar segregation, in which the fibrillar components disappeared, and it produced islets, consisting of dense fibrillar materials, in the nucleoplasm. Ag-NORs observed on the fibrillar components in control nucleoli were translocated onto the dense fibrillar materials in the nucleoplasm. Although scattering was preferentially found in the cells synthesizing DNA, the scintillation assay of DNA/RNA kinetics suggested that scattering was related to the inhibition of RNA synthesis. These results imply that norethindrone preferentially interacts with intranucleolar DNA when its duplication is occurring and then interferes with rRNA synthesis. Scattering of Ag-NORs might not be caused by the hormonal activity of these agents but by a pharmacological effect derived from their molecular structures.

摘要

我们研究了性类固醇对石川细胞中银染核仁组织区(Ag-NORs)和DNA/RNA动力学的影响。炔诺酮及其异构体异炔诺酮专门导致Ag-NORs从核仁分散到核基质中。在所测试的其他性类固醇中,包括孕激素、雄激素和雌激素化合物,未出现这种效应。炔诺酮诱导的核嗜银物质以及核仁嗜银物质既不是DNA也不是RNA,而是蛋白质。电子显微镜显示炔诺酮导致核仁分离,其中纤维成分消失,并在核质中产生由致密纤维物质组成的小岛。在对照核仁的纤维成分上观察到的Ag-NORs转移到了核质中的致密纤维物质上。尽管在合成DNA的细胞中优先发现分散现象,但DNA/RNA动力学的闪烁测定表明,分散与RNA合成的抑制有关。这些结果表明,炔诺酮在其复制发生时优先与核仁内的DNA相互作用,然后干扰rRNA合成。Ag-NORs的分散可能不是由这些药物的激素活性引起的,而是由其分子结构产生的药理作用引起的。

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