Cyp2E1激活导致肝癌的不良后果途径

Francina Webster, I. Lambert, C. Yauk
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引用次数: 4

摘要

目前的AOP描述了导致肝癌的Cyp2E1的延长激活。Cyp2E1是一种细胞色素P450单加氧酶,生物激活超过85种底物,从而产生亲电代谢物和氧化应激。这些底物对其活性代谢物的单氧作用,以及在代谢过程中产生的伴随氧化应激,会造成健康风险,因为它们会导致肝毒性,并经常导致肝癌。当Cyp2E1结合底物时发生MIE。Cyp2E1催化循环容易解耦,产生氧化应激(KE1),底物单氧化产生反应性代谢物。活性氧和代谢物都会引起细胞毒性(KE2)。然而,在损伤后,肝脏能够通过细胞增殖的增加来自我再生(KE3)。在Cyp2E1慢性激活的条件下,活性氧水平的过度慢性增加和细胞死亡,以及随后的细胞增殖失调,导致肿瘤形成(AO)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adverse Outcome Pathway on Cyp2E1 activation leading to liver cancer
The present AOP describes the prolonged activation of Cyp2E1 resulting in liver cancer. Cyp2E1 is a cytochrome P450 mono-oxygenase that bioactivates over 85 substrates, thereby creating electrophilic metabolites and oxidative stress. Mono-oxygenation of these substrates to their reactive metabolites, and the accompanying oxidative stress produced during metabolism, pose health risks because they lead to hepatotoxicity and, often, to liver cancer. The MIE occurs when Cyp2E1 binds a substrate. The Cyp2E1 catalytic cycle is prone to decoupling, which produces oxidative stress (KE1), and mono-oxidation of substrates produces reactive metabolites. Both reactive oxygen species and metabolites cause cytotoxicity (KE2). However, following injury, the liver is able to regenerate itself through an increase in cellular proliferation (KE3). Under conditions of chronic activation of Cyp2E1, excessive chronic increases in levels of reactive oxygen species and cell death, and subsequent dysregulated cellular proliferation, leads to tumour formation (AO).
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