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Transcriptional suppression of cytochrome P450 genes by endogenous and exogenous chemicals.

机译:内源性和外源性化学物质对细胞色素P450基因的转录抑制。

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摘要

This article is an invited report of a symposium sponsored by the Division for Drug Metabolism of the American Society for Pharmacology and Experimental Therapeutics held at Experimental Biology 2003 in San Diego, California, April 11-15, 2003. Several members of the cytochrome P450 (P450) superfamily are induced after exposure to a variety of chemical signals, and we have gained considerable mechanistic insight into these processes over the past four decades. In addition, the expression of many P450s is suppressed in response to various endogenous and exogenous chemicals; however, relatively little is known about the molecular mechanisms involved. The goal of this symposium was to critically examine our current understanding of molecular mechanisms involved in transcriptional suppression of CYP genes by endogenous and exogenous chemicals. Specific examples were drawn from the following chemical categories: polycyclic and halogenated aromatic hydrocarbon environmental toxicants, inflammatory mediators,the endogenous sterol dehydroepiandrosterone and peroxisome proliferators, and bile acids. Multiple molecular mechanisms are involved in transcriptional suppression, and these processes often involve rather complex cascades of transcription factors and other regulatory proteins. Mechanistic studies of CYP gene suppression can enhance our understanding of how organisms respond to xenobiotics as well as to perturbations in endogenous chemicals involved in maintaining homeostasis.
机译:本文是2003年4月11日至15日在加利福尼亚州圣地亚哥举行的2003年实验生物学大会上由美国药理学和实验治疗学协会药物代谢学分会主办的研讨会的邀请报告。细胞色素P450( P450)超家族是在暴露于多种化学信号后诱导而来的,并且在过去的40年中,我们已经对这些过程获得了相当多的机理认识。另外,响应于各种内源性和外源性化学物质,许多P450的表达受到抑制。然而,对所涉及的分子机制知之甚少。本次研讨会的目的是批判性地检查我们目前对内源性和外源性化学物质抑制CYP基因转录的分子机制的理解。具体实例选自以下化学类别:多环和卤代芳烃环境毒物,炎症介质,内源性固醇脱氢表雄酮和过氧化物酶体增生剂以及胆汁酸。转录抑制涉及多种分子机制,并且这些过程通常涉及相当复杂的转录因子和其他调节蛋白的级联反应。 CYP基因抑制的机理研究可以增进我们对生物如何响应异种生物以及维持动态平衡的内源性化学物质的扰动的理解。

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