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丝裂原活化蛋白激酶在芳烃受体信号传导中的作用。

Role of mitogen-activated protein kinases in aryl hydrocarbon receptor signaling.

作者信息

Henklová Pavla, Vrzal Radim, Ulrichová Jitka, Dvorák Zdenek

机构信息

Department of Medical Chemistry and Biochemistry, Faculty of Medicine and Dentistry, Palacky University, Hnevotínská 3, 775 15 Olomouc, Czech Republic.

出版信息

Chem Biol Interact. 2008 Mar 27;172(2):93-104. doi: 10.1016/j.cbi.2007.12.005. Epub 2007 Dec 31.

Abstract

Human populations are increasingly exposed to a number of environmental pollutants such as polycyclic aromatic hydrocarbons, polychlorinated biphenyls and dioxins. These compounds are activators of the aryl hydrocarbon receptor (AhR) that controls the expression of many genes including those for detoxification enzymes. The regulatory mechanisms of AhR are multi-factorial and include phosphorylation by various protein kinases. Significant progress in the research of mitogen-activated protein kinases (MAPKs) has been achieved in the last decade. Isolated reports have been published on the role of MAPKs in AhR functions and vice versa, with activation of MAPKs by AhR ligands. This mini-review summarizes current knowledge on the mutual interactions between MAPKs and AhR. The majority of studies has been done on cancer-derived cell lines that have impaired cell cycle regulation and lacks the complete detoxification apparatus. We emphasize the importance of the future studies that should be done on non-transformed cells to distinguish the role of MAPKs in cancer and normal cells. Primary cultures of human or rodent hepatocytes that are equipped with a fully functional biotransformation battery or xenobiotics-metabolizing extra-hepatic tissues should be the models of choice, as the results in our experiments confirm.

摘要

人类越来越多地暴露于多种环境污染物中,如多环芳烃、多氯联苯和二恶英。这些化合物是芳烃受体(AhR)的激活剂,AhR可控制包括解毒酶基因在内的许多基因的表达。AhR的调控机制是多因素的,包括各种蛋白激酶的磷酸化作用。在过去十年中,丝裂原活化蛋白激酶(MAPK)的研究取得了重大进展。关于MAPK在AhR功能中的作用以及反之亦然,即AhR配体对MAPK的激活作用,已有单独的报道发表。这篇小型综述总结了目前关于MAPK与AhR之间相互作用的知识。大多数研究是在癌症衍生的细胞系上进行的,这些细胞系的细胞周期调控受损且缺乏完整的解毒机制。我们强调未来应在未转化细胞上进行研究的重要性,以区分MAPK在癌细胞和正常细胞中的作用。配备有功能齐全的生物转化系统或可代谢外源性物质的肝外组织的人或啮齿动物肝细胞原代培养物应是首选模型,正如我们实验中的结果所证实的那样。

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