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多胺生物合成酶作为癌症化疗的靶点。

Polyamine biosynthetic enzymes as targets in cancer chemotherapy.

作者信息

Heby O, Oredsson S M, Kanje M

出版信息

Adv Enzyme Regul. 1984;22:243-64. doi: 10.1016/0065-2571(84)90017-7.

Abstract

In this chapter we focus attention on recent developments in the biosynthesis of putrescine, spermidine and spermine and their linkage to salvage pathways of methionine and adenine nucleotide synthesis. We describe the use of specific inhibitors of the polyamine biosynthetic enzymes for studying the role of polyamines in cell growth and division as well as in cell differentiation. Some novel findings are presented which suggest that part of the inhibitory action that polyamine synthesis inhibitors exert on DNA synthesis may be due to the accumulation of ADP and ATP. We show that polyamine synthesis inhibitors are capable of inducing terminal differentiation of neoplastic cells to forms with no further proliferative potential, and briefly discuss the potential use of this approach in cancer chemotherapy.

摘要

在本章中,我们重点关注腐胺、亚精胺和精胺生物合成的最新进展,以及它们与蛋氨酸和腺嘌呤核苷酸合成的补救途径的联系。我们描述了使用多胺生物合成酶的特异性抑制剂来研究多胺在细胞生长、分裂以及细胞分化中的作用。文中呈现了一些新发现,这些发现表明多胺合成抑制剂对DNA合成产生的部分抑制作用可能是由于ADP和ATP的积累。我们表明多胺合成抑制剂能够诱导肿瘤细胞终末分化为不再具有增殖潜力的形式,并简要讨论了这种方法在癌症化疗中的潜在应用。

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