Skoči na glavni sadržaj

Arhiv za higijenu rada i toksikologiju, Vol. 60 No. 2, 2009.

Pregledni rad

https://doi.org/10.2478/10004-1254-60-2009-1885

Genetic Polymorphism of Metabolic Enzymes P450 (CYP) as a Susceptibility Factor for Drug Response, Toxicity, and Cancer Risk

Nada Božina orcid id orcid.org/0000-0001-6016-1699 ; Clinical Institute of Laboratory Diagnosis, Zagreb University School of Medicine and University Hospital Centre Zagreb, Zagreb, Croatia
Vlasta Bradamante ; Department of Pharmacology, Zagreb University School of Medicine, Zagreb, Croatia
Mila Lovrić ; Clinical Institute of Laboratory Diagnosis, Zagreb University School of Medicine and University Hospital Centre Zagreb, Zagreb, Croatia

Puni tekst: engleski pdf 168 Kb

str. 217-242

preuzimanja: 10.617

citiraj

Sažetak

The polymorphic P450 (CYP) enzyme superfamily is the most important system involved in the biotransformation of many endogenous and exogenous substances including drugs, toxins, and carcinogens. Genotyping for CYP polymorphisms provides important genetic information that help to understand the effects of xenobiotics on human body. For drug metabolism, the most important polymorphisms are those of the genes coding for CYP2C9, CYP2C19, CYP2D6, and CYP3A4/5, which can result in therapeutic failure or severe adverse reactions. Genes coding for CYP1A1, CYP1A2, CYP1B1, and CYP2E1 are among the most responsible for the biotransformation of chemicals, especially for the metabolic activation of pre-carcinogens. There is evidence of association between gene polymorphism and cancer susceptibility. Pathways of carcinogen metabolism are complex, and are mediated by activities of multiple genes, while single genes have a limited impact on cancer risk. Multigenic approach in addition to environmental determinants in large sample studies is crucial for a reliable evaluation of any moderate gene effect. This article brings a review of current knowledge on the relations between the polymorphisms of some CYPs and drug activity/toxicity and cancer risk.

Ključne riječi

cancer risk; cytochrome P450; drug metabolism; genotyping; pharmacogenomics; polymorphic allele; xenobiotics

Hrčak ID:

38412

URI

https://hrcak.srce.hr/38412

Datum izdavanja:

12.6.2009.

Podaci na drugim jezicima: hrvatski

Posjeta: 13.869 *