首页> 外文期刊>Drug Metabolism Reviews >The Val158Met polymorphism in COMT gene and cancer risk: role of endogenous and exogenous catechols
【24h】

The Val158Met polymorphism in COMT gene and cancer risk: role of endogenous and exogenous catechols

机译:COMT基因的Val158met多态性和癌症风险:内源性和外源性儿茶酚的作用

获取原文
获取原文并翻译 | 示例
           

摘要

Catechol-O-methyltransferase, COMT, is an important phase II enzyme catalyzing the transfer of a methyl-group from S-adenosylmethionine to a catechol-containing substrate molecule. A genetic variant Val158Met in the COMT gene leads to a several-fold decrease in the enzymatic activity giving rise to the accumulation of potentially carcinogenic endogenous catechol estrogens and their reactive intermediates and increasing thus the risk of tumorigenesis. However, numerous association studies between the COMT genotype and susceptibility to various malignancies have shown inconsistent and controversial findings indicating that additional gene-gene and gene-environment interactions might be crucial in modulating the physiological role of the COMT. In this review article, the important contribution of dietary catechol-containing flavonoids to modification of the relationships between the COMT genotype and cancer risk is discussed. Whereas, the diverse anticancer activities of common phytochemicals, such as green tea polyphenols, quercetin, fisetin or luteolin, can be markedly changed (both decreased or increased) by the COMT-mediated O-methylation of these exogenous substrates, flavonoids can also behave as potent inhibitors of the COMT enzyme slowing detoxification of endogenous catechol estrogens. Such a many-featured functioning of the COMT and its complex regulation by several different genetic and environmental factors, including plant-based food ingredients, emphasizes the necessity to further stratify the association studies between the COMT genotype and tumor risk by consumption of catechol-containing dietary flavonoids. Currently, it can be only speculated that some of the possible associations might be masked by the regular intake of specific food polyphenols, taking effect in certain communities or populations.
机译:CateChol-O-甲基转移酶COMT是催化来自S-亚苯基甲基硫氨酸的甲基 - 基团转移到含儿茶酚的底物分子的重要相二酶。 COMT基因中的遗传变异Val158met导致酶活性的几倍降低,从而产生潜在的致癌内源性儿茶酚雌激素的积累和其反应性中间体,因此增加肿瘤发生的风险。然而,COMT基因型和对各种恶性肿瘤的易感性之间的许多关联研究表明,表明额外的基因 - 基因和基因 - 环境相互作用可能对调节COMT的生理作用可能是至关重要的。在本文中,讨论了含膳食儿茶酚的黄酮对COMT基因型与癌症风险之间关系进行修饰的重要贡献。虽然,通过这些外源性基材的COMT介导的O-甲基化,可以显着改变(绿茶多酚,槲皮素,槲皮素,槲皮素,槲皮素,槲皮素,Fisetin或叶氏菌素等多种植物化学物质,如绿茶多酚,槲皮素,植物素或叶氏菌素),但黄酮类化合物也可以表现为具有内源性儿茶酚雌激素的COMT酶的有效抑制剂。这种多种遗传和环境因素包括植物的食品成分的这种多种功能和其复杂的调节,强调必须进一步分析COMT基因型和肿瘤风险之间的关联研究,通过消费的儿茶酚含量消耗膳食类黄酮。目前,可以推测一些可能的联合可能被特定食物多酚的定期摄入量掩盖,从某些社区或人群中生效。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号