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咖啡成分对N-乙酰转移酶和谷胱甘肽S-转移酶的修饰:对癌症风险的潜在影响

Modification of N-acetyltransferases and glutathione S-transferases by coffee components: possible relevance for cancer risk.

作者信息

Huber Wolfgang W, Parzefall Wolfram

机构信息

Institut für Krebsforchung, Department of Toxicology, Medical University of Vienna, Austria.

出版信息

Methods Enzymol. 2005;401:307-41. doi: 10.1016/S0076-6879(05)01020-7.

Abstract

Enzymes of xenobiotic metabolism are involved in the activation and detoxification of carcinogens and can play a pivotal role in the susceptibility of individuals toward chemically induced cancer. Differences in such susceptibility are often related to genetically predetermined enzyme polymorphisms but may also be caused by enzyme induction or inhibition through environmental factors or in the frame of chemopreventive intervention. In this context, coffee consumption, as an important lifestyle factor, has been under thorough investigation. Whereas the data on a potential procarcinogenic effect in some organs remained inconclusive, epidemiology has clearly revealed coffee drinkers to be at a lower risk of developing cancers of the colon and the liver and possibly of several other organs. The underlying mechanisms of such chemoprotection, modifications of xenobiotic metabolism in particular, were further investigated in rodent and in vitro models, as a result of which several individual chemoprotectants out of the >1000 constituents of coffee were identified as well as some strongly metabolized individual carcinogens against which they specifically protected. This chapter discusses the chemoprotective effects of several coffee components and whole coffee in association with modifications of the usually protective glutathione-S-transferase (GST) and the more ambivalent N-acetyltransferase (NAT). A key role is played by kahweol and cafestol (K/C), two diterpenic constituents of the unfiltered beverage that were found to reduce mutagenesis/tumorigenesis by strongly metabolized compounds, such as 2-amino-1-methyl-6-phenylimidazo-[4,5-b]pyridine, 7,12-dimethylbenz[a]anthracene, and aflatoxin B(1), and to cause various modifications of xenobiotic metabolism that were overwhelmingly beneficial, including induction of GST and inhibition of NAT. Other coffee components such as polyphenols and K/C-free coffee are also capable of increasing GST and partially of inhibiting NAT, although to a somewhat lesser extent.

摘要

外源性物质代谢酶参与致癌物的激活和解毒过程,在个体对化学诱导癌症的易感性方面起着关键作用。这种易感性的差异通常与基因预先决定的酶多态性有关,但也可能由环境因素或化学预防干预过程中的酶诱导或抑制引起。在这种背景下,咖啡消费作为一个重要的生活方式因素,受到了深入研究。尽管关于某些器官潜在的促癌作用的数据尚无定论,但流行病学研究清楚地表明,咖啡饮用者患结肠癌、肝癌以及可能其他几种器官癌症的风险较低。在啮齿动物和体外模型中进一步研究了这种化学保护的潜在机制,特别是外源性物质代谢的改变,结果从咖啡的1000多种成分中鉴定出了几种单独的化学保护剂,以及一些它们能特异性保护的强代谢个体致癌物。本章讨论了几种咖啡成分和全咖啡的化学保护作用,以及与通常具有保护作用的谷胱甘肽 - S - 转移酶(GST)和更具争议性的N - 乙酰转移酶(NAT)的改变之间的关系。咖啡豆醇和咖啡醇(K/C)起着关键作用,它们是未过滤咖啡饮料中的两种二萜成分,被发现可通过强烈代谢的化合物(如2 - 氨基 - 1 - 甲基 - 6 - 苯基咪唑[4,5 - b]吡啶、7,12 - 二甲基苯并[a]蒽和黄曲霉毒素B1)减少诱变/肿瘤发生,并引起外源性物质代谢的各种改变,这些改变绝大多数是有益的,包括诱导GST和抑制NAT。其他咖啡成分,如多酚和不含K/C的咖啡,也能够增加GST并部分抑制NAT,尽管程度稍小。

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