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鸟氨酸脱羧酶作为化疗靶点。

Ornithine decarboxylase as target of chemotherapy.

作者信息

Heby O

出版信息

Adv Enzyme Regul. 1985;24:103-24. doi: 10.1016/0065-2571(85)90072-x.

Abstract

Ornithine decarboxylase is a key enzyme in polyamine synthesis and growth of mammalian cells. In this chapter I review recent reports on the purification and properties of the pure enzyme, and on the localization, synthesis and regulation of the enzyme in the cell. The use of monospecific antibodies, radiolabeled irreversible inhibitors and cDNA clones for studying enzyme localization, turnover and regulation, is briefly described. This first part is meant to serve as a basis for the analysis of ornithine decarboxylase as a target of chemotherapy. A selection of the most potent inhibitors of ornithine decarboxylase is presented and the effects of some of these in cell culture, in animals and in the clinical setting are reviewed.

摘要

鸟氨酸脱羧酶是哺乳动物细胞多胺合成和生长中的关键酶。在本章中,我将综述有关该纯酶的纯化和性质,以及该酶在细胞中的定位、合成和调节的最新报道。简要描述了使用单特异性抗体、放射性标记的不可逆抑制剂和cDNA克隆来研究酶的定位、周转和调节。第一部分旨在作为分析鸟氨酸脱羧酶作为化疗靶点的基础。列出了一些最有效的鸟氨酸脱羧酶抑制剂,并综述了其中一些在细胞培养、动物和临床环境中的作用。

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Ornithine decarboxylase as target of chemotherapy.鸟氨酸脱羧酶作为化疗靶点。
Adv Enzyme Regul. 1985;24:103-24. doi: 10.1016/0065-2571(85)90072-x.

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