Revisão Revisado por pares

Carcinogenic polycyclic aromatic hydrocarbon‐DNA adducts and mechanism of action

2005; Wiley; Volume: 45; Issue: 2-3 Linguagem: Inglês

10.1002/em.20095

ISSN

1098-2280

Autores

William M. Baird, Louisa A. Hooven, Brinda Mahadevan,

Tópico(s)

Effects and risks of endocrine disrupting chemicals

Resumo

Abstract Polycyclic aromatic hydrocarbons (PAHs) are a class of widespread environmental carcinogens. Most of our knowledge of their mechanisms of metabolic activation to DNA‐binding “ultimate carcinogenic” metabolites has come from analysis of the DNA interaction products formed by these highly reactive intermediates. Studies of their role in forming DNA‐binding intermediates identical to those formed in vivo from the PAH itself have also allowed identification of the particular cytochrome P450 enzymes involved in activating various structural classes of carcinogenic PAHs. It has been established that PAHs, after metabolic activation in vivo, are capable of inducing mutations in oncogenes and, by inducing multiple mutations, may result in tumors. PAHs also cause changes in cellular gap‐junction communication similar to those caused by the tumor promoter 12‐ O ‐tetradecanoylphorbol‐13‐acetate. Thus, PAHs may also act through a promotional mechanism in addition to serving as tumor initiators. Previous studies on these mechanisms are described and summarized. Environ. Mol. Mutagen., 2005. © 2005 Wiley‐Liss, Inc.

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