Abstract

In this study, the frequencies of CYP1A1, GSTM1, and GSTT1 gene polymorphisms were determined in 133 healthy individuals from Ouangolodougou, a small rural town situated in the north of the Ivory Coast. As appeared in several published studies, ethnic differences in these frequencies have been found to play an important role in the metabolism of a relevant number of human carcinogens. In the studied sample, the frequencies of Ile/Ile (wild type), Ile/Val (heterozygous variant), and Val/Val (homozygous variant) CYP1A1 genotypes were 0.271, 0.692, and 0.037, respectively. Frequencies of GSTM1 and GSTT1 null genotypes were 0.361 and 0.331, respectively. No significant differences were noted between men and women. In contrast to published data for Africans, CYP1A1 *Val Allele frequency (0.383) was significantly high (p < 0.001) in this specific population. For the GSTT1 null genotype, no differences were found between the studied and other African populations, the contrary to what occurred for the GSTM1 null genotype in relation to Gambia and Egypt.

Highlights

  • Several polymorphic genetic systems have been used to study human genetic variation

  • We report for a sample from the Ivory Coast on the frequencies of three polymorphic metabolic genes that have been found to play an important role in the metabolism of a relevant number of human carcinogens: the Cytochrome P450 1A1 (CYP1A1), the Glutathione S-transferases (GST) T1 and the GSTM1 genes

  • The CYP1A1 gene is a component of the phase I cytochrome P450 superfamily, which plays a primary role in the metabolism of polycyclic aromatic hydrocarbons

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Summary

Introduction

We report for a sample from the Ivory Coast on the frequencies of three polymorphic metabolic genes that have been found to play an important role in the metabolism of a relevant number of human carcinogens: the Cytochrome P450 1A1 (CYP1A1), the Glutathione S-transferases (GST) T1 and the GSTM1 genes. GSTT1 and GSTM1 genes have long been known to be polymorphic in humans by the deletion of a segment of DNA, with the subsequent lack of protein synthesis in homozygous individuals.

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