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

CYP2E1 GSTM1 GSTT1 Nasopharyngeal Carcinoma North Africa metabolizing enzymes

Journal

Annals of human genetics
ISSN: 1469-1809
Titre abrégé: Ann Hum Genet
Pays: England
ID NLM: 0416661

Informations de publication

Date de publication:
15 Apr 2024
Historique:
revised: 08 03 2024
received: 02 08 2023
accepted: 02 04 2024
medline: 16 4 2024
pubmed: 16 4 2024
entrez: 16 4 2024
Statut: aheadofprint

Résumé

Nasopharyngeal 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. A 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. The 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. In this large studied North African population, our findings suggest that the functional CYP2E1, CYP2A6, GSTM1 and GSTT1 variations did not influence NPC susceptibility.

Sections du résumé

BACKGROUND BACKGROUND
Nasopharyngeal 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.
METHODS METHODS
A 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.
RESULTS RESULTS
The 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.
CONCLUSION CONCLUSIONS
In this large studied North African population, our findings suggest that the functional CYP2E1, CYP2A6, GSTM1 and GSTT1 variations did not influence NPC susceptibility.

Identifiants

pubmed: 38622954
doi: 10.1111/ahg.12562
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Institut de Recherche sur le Cancer
ID : 201932
Organisme : Institut Pasteur
Organisme : International Agency for Research on Cancer
Organisme : National Scientific and Technical Research Centre

Informations de copyright

© 2024 University College London (UCL) and John Wiley & Sons Ltd.

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Auteurs

Imane El Alami (IE)

Laboratory of Viral Oncology, Institut Pasteur du Maroc, Casablanca, Morocco.
Laboratory of Immunology and Biodiversity, Faculty of Sciences Ain Chock, Hassan II University, Casablanca, Morocco.

Wafa Khaali (W)

Laboratory of Viral Oncology, Institut Pasteur du Maroc, Casablanca, Morocco.
Departement of Biology, Faculty of Sciences, Abdelmalek Essaadi University, Tetouan, Morocco.

Majida Jalbout (M)

Anti-Tumor Therapeutic Targeting Laboratory, Faculty of Sciences, Lebanese University, Hadath, Lebanon.
Immunogenetic Pathology Laboratory, Faculty of Sciences, Lebanese University, Fanar, Lebanon.

Amina Gihbid (A)

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

Wided Ben Ayoub (WB)

Association Tunisienne de Lutte Contre le Cancer, Tunis, Tunisia.

Abdellatif Benider (A)

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

Selma Mohamed Brahim (SM)

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

Mokhtar Hamdi Cherif (MH)

Service d'épidémiologie, CHU de Sétif, Sétif, Algeria.

Nadia Benchakroun (N)

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

Mohammed El Mzibri (ME)

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

El Khalil Ben Driss (EKB)

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

Khalid Belghmi (K)

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

Marilys Corbex (M)

WHO Regional Office for Europe, Copenhagen, Denmark.

Meriem Khyatti (M)

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

Classifications MeSH