Cases of nasopharyngeal carcinoma (NPC) from North Africa show an unusual bimodal age distribution. As elsewhere, the tumor is closely associated with the presence of Epstein-Barr virus (EBV). The expression of EBV genes and c-onc genes was studied i n biopsy specimens from tumors at different clini
XRCC1 and hOGG1 genes and risk of nasopharyngeal carcinoma in North African countries
✍ Scribed by Nadia Laantri; Majida Jalbout; Meriem Khyatti; Wided Ben Ayoub; Sami Dahmoul; Messaoud Ayad; Wided Bedadra; Meriem Abdoun; Sarah Mesli; Mostafa Kandil; Mokhtar Hamdi-Cherif; Kada Boualga; Noureddine Bouaouina; Lotfi Chouchane; Abdellatif Benider; Farhat Ben-Ayed; David Goldgar; Marilys Corbex
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 74 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0899-1987
- DOI
- 10.1002/mc.20754
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Although genetic susceptibility to nasopharyngeal carcinoma (NPC) has been recognized for a long time, little is known about the responsible genes. X‐Ray repair cross‐complementing protein 1 (XRCC1) and human 8‐oxo‐guanine glycosylase 1 (hOGG1) genes are involved in deoxyribonucleic acid (DNA) repair and were found associated with NPC risk in three Asian case–control studies. The objective of the present study was to test these genes in a sample from North Africa, one of the major NPC endemic regions in the world. Three single nucleotide polymorphisms (SNPs) in the XRCC1 gene and one SNP in the hOGG1 gene were genotyped in 598 NPC cases from Morocco, Algeria, and Tunisia and 545 controls frequency matched by recruitment center, age, sex, and urban/rural household. The genotype and allelic distributions for the hOGG1 ^326^Ser/Cys SNP and for the XRCC1 ^399^Arg/Trp, ^280^Arg/His, and ^194^Arg/Trp SNPs did not differ significantly among NPC cases and controls. The XRCC1 ^194^Trp allele frequency was significantly lower in the North African population than in Asian population (f = 0.04 vs. 0.31 in Cantonese Chinese and 0.21 Han Chinese). The hOGG1 ^326^Ser allele frequency was significantly higher in the North African population (f = 0.73) than in Asian populations (f = 0.39 in Taiwanese). The results of the present study obtained from a large sample indicate that the XRCC1 and hOGG1 genes are unlikely to play a role in the susceptibility to NPC in North Africans. Our results do not corroborate those found in Asian population on smaller samples. Mol. Carcinog. © 2011 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract North Africa is one of the major Nasopharyngeal Carcinoma (NPC) endemic regions. Specific food items unique to this area were implicated to be associated with NPC risk, but results were inconsistent. Here we have performed a large‐scale case‐control study in the Maghrebian population fr
## Abstract ## BACKGROUND. Tobacco smoke contains numerous carcinogens that cause DNA damage, including oxidative lesions that are removed effectively by the base‐excision repair (BER) pathway, in which adenosine diphosphate ribosyl transferase (ADPRT), x‐ray repair cross‐complementing 1 (XRCC1),
## Abstract Two non‐synonymous polymorphisms Arg194Trp and Arg399Gln in the DNA‐base excision repair gene X‐ray repair cross‐complementing group 1 (__XRCC1__) have been implicated in risk for esophageal cancer. However, the results from different studies remain controversial. The present meta‐analy
Ser326Cys polymorphism in the hOGG1 gene, which is involved in the repair of 8-hydroxyguanine in oxidatively damaged DNA, has been identified and the variant genotype appears to be related to susceptibility to certain cancers. We investigated the association between Ser326Cys polymorphism and squamo
## Abstract Esophageal squamous cell carcinoma (ESCC), which is prevalent in China, is believed to be induced by environmental carcinogens. Accumulating evidence has shown that individual variation in DNA repair capacity resulting from genetic polymorphism influences risk of environmental carcinoge