Genetic variations in CYP2A6, CYP2E1, GSTM1, GSTT1 genes and the risk of Nasopharyngeal carcinoma in North African population

Author:

Alami Imane EL12ORCID,Khaali Wafa13,Jalbout Majida45,Gihbid Amina1,Ayoub Wided Ben6,Benider Abdellatif7,Brahim Selma Mohamed1,Cherif Mokhtar Hamdi8,Benchakroun Nadia7,Mzibri Mohammed El9,Driss El Khalil Ben3,Belghmi Khalid2,Corbex Marilys10,Khyatti Meriem1

Affiliation:

1. Laboratory of Viral Oncology Institut Pasteur du Maroc Casablanca Morocco

2. Laboratory of Immunology and Biodiversity, Faculty of Sciences Ain Chock Hassan II University Casablanca Morocco

3. Departement of Biology, Faculty of Sciences Abdelmalek Essaadi University Tetouan Morocco

4. Anti‐Tumor Therapeutic Targeting Laboratory Faculty of Sciences Lebanese University Hadath Lebanon

5. Immunogenetic Pathology Laboratory, Faculty of Sciences Lebanese University Fanar Lebanon

6. Association Tunisienne de Lutte Contre le Cancer Tunis Tunisia

7. Mohammed VI Center for Cancer Treatment Ibn Rochd University Hospital Casablanca Morocco

8. Service d'épidémiologie CHU de Sétif Sétif Algeria

9. Biology and Medical Research Unit, National Center of Energy Nuclear Sciences and Techniques Rabat Rabat Morocco

10. WHO Regional Office for Europe Copenhagen Denmark

Abstract

AbstractBackgroundNasopharyngeal carcinoma (NPC) is a multifactorial malignancy associated with both genetic and environmental factors. Polymorphic deletions of the phase I and phase II genes involved in the detoxification of potential carcinogens may be a risk factor for nasopharyngeal carcinoma. In this study, we investigated the relationship between CYP2E1 (rs3813867), CYP2A6, GSTM1(rs1183423000) and GSTT1(rs1601993659) gene variations and NPC risk in North African countries with the highest incidence of NPC (Morocco, Algeria and Tunisia). and the evaluation of the potential use of these variants as potential biomarkers for NPC management.MethodsA total of 600 NPC cases and 545 controls frequency‐matched on ethnicity, sex, age and childhood household type, were recruited from three North African countries (Morocco, Algeria and Tunisia) and analysed. Genotyping of CYP2A6 and CYP2E1(rs3813867) was performed by polymerase chain reaction restriction (PCR)‐fragment length polymorphism (RFLP) analysis and the GSTM1 (rs1183423000) and GSTT1(rs1601993659) genetic variations were evaluated using the PCR technique.ResultsThe genotype distributions of CYP2E1(rs3813867), CYP2A6, GSTM1(rs1183423000) and GSTT1(rs1601993659) genotypes did not differ significantly among NPC cases and controls (p > 0.05). Furthermore, our data did not reveal any association with smoking and the studied variants, even when the samples were stratified by the duration period of smoking.ConclusionIn this large studied North African population, our findings suggest that the functional CYP2E1, CYP2A6, GSTM1 and GSTT1 variations did not influence NPC susceptibility.

Funder

Institut Pasteur

Centre International de Recherche sur le Cancer

Publisher

Wiley

Reference35 articles.

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3. No association between genetic polymorphisms of CYP1A1, GSTM1, GSTT1, GSTP1, NAT2, and nasopharyngeal carcinoma in Taiwan;Cheng Y.‐J.;Cancer Epidemiology, Biomarkers & Prevention,2003

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