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人芳香胺 N-乙酰基转移酶 1:一种药物代谢酶和药物靶点?

Human arylamine N-acetyltransferase 1: a drug-metabolizing enzyme and a drug target?

机构信息

Univ Paris Diderot-Paris 7, Unité de Biologie Fonctionnelle et Adaptative, CNRS EAC 4413, 75013, Paris, France.

出版信息

Curr Drug Targets. 2010 Jun;11(6):759-66. doi: 10.2174/138945010791170905.

Abstract

Human arylamine N-acetyltransferase 1 (NAT1) is a phase II xenobiotic-metabolizing enzyme (XME) involved in the biotransformation of many aromatic and heterocyclic amines. This XME plays key roles in both the detoxification and/or bioactivation of numerous drugs and carcinogens. NAT1 is polymorphic and displays a large tissue distribution. NAT1 activity have been extensively studied because of its potential role in the biotransformation of important carcinogens. Several recent studies suggest that NAT1 may have a role in breast cancer progression. Indeed, this XME has been shown to affect the growth and drug resistance of breast cancer cells and appears as a marker in human estrogen receptor positive breast cancer. In addition, it has been shown that this enzyme is inhibited in vivo by cancer drugs such as cisplatin or tamoxifen. Recent published data suggest that NAT1 could be of therapeutic interest for cancer. We provide here an overview on the putative involvement of NAT1 in cancer and its possible role as a drug target.

摘要

人类芳香族胺 N-乙酰基转移酶 1(NAT1)是一种 II 相异生物代谢酶(XME),参与许多芳香族和杂环胺的生物转化。这种 XME 在许多药物和致癌物的解毒和/或生物活化中起着关键作用。NAT1 是多态的,具有广泛的组织分布。由于其在重要致癌物生物转化中的潜在作用,NAT1 活性已得到广泛研究。最近的几项研究表明,NAT1 可能在乳腺癌的进展中起作用。事实上,已经表明这种 XME 会影响乳腺癌细胞的生长和耐药性,并作为人类雌激素受体阳性乳腺癌的标志物出现。此外,已经表明该酶在体内被顺铂或他莫昔芬等癌症药物抑制。最近发表的数据表明,NAT1 可能对癌症具有治疗意义。我们在这里概述了 NAT1 在癌症中的潜在作用及其作为药物靶点的可能作用。

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