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Cancer Activation and Polymorphisms of Human Cytochrome P450 1B1

Authors
Chun, Young-JinKim, Donghak
Issue Date
Apr-2016
Publisher
KOREAN SOC TOXICOLOGY
Keywords
Cytochrome P450 1B1; Cancer activation; Polymorphism
Citation
TOXICOLOGICAL RESEARCH, v.32, no.2, pp 89 - 93
Pages
5
Journal Title
TOXICOLOGICAL RESEARCH
Volume
32
Number
2
Start Page
89
End Page
93
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/7058
DOI
10.5487/TR.2016.32.2.089
ISSN
1976-8257
2234-2753
Abstract
Human cytochrome P450 enzymes (P450s, CYPs) are major oxidative catalysts that metabolize various xenobiotic and endogenous compounds. Many carcinogens induce cancer only after metabolic activation and P450 enzymes play an important role in this phenomenon. P450 1B1 mediates bioactivation of many procarcinogenic chemicals and carcinogenic estrogen. It catalyzes the oxidation reaction of polycyclic aromatic carbons, heterocyclic and aromatic amines, and the 4-hydroxylation reaction of 17 beta-estradiol. Enhanced expression of P450 1B1 promotes cancer cell proliferation and metastasis. There are at least 25 polymorphic variants of P450 1B1 and some of these have been reported to be associated with eye diseases. In addition, P450 1B1 polymorphisms can greatly affect the metabolic activation of many procarcinogenic compounds. It is necessary to understand the relationship between metabolic activation of such substances and P450 1B1 polymorphisms in order to develop rational strategies for the prevention of its toxic effect on human health.
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