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多胺代谢在癌变中的作用:化疗和化学预防的潜在靶点。

Polyamine catabolism in carcinogenesis: potential targets for chemotherapy and chemoprevention.

机构信息

The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Bunting Blaustein Bldg., Room 551, 1650 Orleans Street, Baltimore, MD, 21287, USA.

出版信息

Amino Acids. 2014 Mar;46(3):511-9. doi: 10.1007/s00726-013-1529-6. Epub 2013 Jun 15.

Abstract

Polyamines, including spermine, spermidine, and the precursor diamine, putrescine, are naturally occurring polycationic alkylamines that are required for eukaryotic cell growth, differentiation, and survival. This absolute requirement for polyamines and the need to maintain intracellular levels within specific ranges require a highly regulated metabolic pathway primed for rapid changes in response to cellular growth signals, environmental changes, and stress. Although the polyamine metabolic pathway is strictly regulated in normal cells, dysregulation of polyamine metabolism is a frequent event in cancer. Recent studies suggest that the polyamine catabolic pathway may be involved in the etiology of some epithelial cancers. The catabolism of spermine to spermidine utilizes either the one-step enzymatic reaction of spermine oxidase (SMO) or the two-step process of spermidine/spermine N (1)-acetyltransferase (SSAT) coupled with the peroxisomal enzyme N (1)-acetylpolyamine oxidase. Both catabolic pathways produce hydrogen peroxide and a reactive aldehyde that are capable of damaging DNA and other critical cellular components. The catabolic pathway also depletes the intracellular concentrations of spermidine and spermine, which are free radical scavengers. Consequently, the polyamine catabolic pathway in general and specifically SMO and SSAT provide exciting new targets for chemoprevention and/or chemotherapy.

摘要

多胺包括精脒、精胺和前体二胺腐胺,是天然存在的阳离子碱性多胺,对真核细胞的生长、分化和存活是必需的。多胺的这种绝对需求以及需要将细胞内水平维持在特定范围内,要求代谢途径具有高度的调控性,以便能够快速响应细胞生长信号、环境变化和应激。虽然多胺代谢途径在正常细胞中受到严格调控,但癌症中多胺代谢的失调是常见的事件。最近的研究表明,多胺分解代谢途径可能参与某些上皮癌的病因。精脒分解为精胺可以通过精脒氧化酶 (SMO) 的一步酶促反应或精脒/精胺 N (1)-乙酰基转移酶 (SSAT) 与过氧化物酶体酶 N (1)-乙酰多胺氧化酶偶联的两步过程进行。这两种分解代谢途径都会产生过氧化氢和一种反应性醛,能够损伤 DNA 和其他关键细胞成分。分解代谢途径还会耗尽细胞内精脒和精胺的浓度,而精脒和精胺是自由基清除剂。因此,多胺分解代谢途径一般和 SMO 和 SSAT 特别为化学预防和/或化疗提供了令人兴奋的新靶点。

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