Polymorphisms of NF B1 and i B α and Their Synergistic Effect on Nasopharyngeal Carcinoma Susceptibility

Abstract

Nasopharyngeal carcinoma (NPC) is a multifactoral and polygenic disease with high prevalence in Southeast Asia and Southern China. Environmental factors and genetic susceptibility play important roles in NPC pathogenesis. In the present study, we tested the hypothesis that single nucleotide polymorphisms (SNPs) in nuclear factor-kappa B (NFB) and its inhibitor (IBα) conferred consistent risks for NPC. Four putatively functional SNPs (NFB1: rs28362491del> A; IBα: rs2233406C>T and rs696G>A) were analyzed to evaluate their associations with NPC risk in total 1590 NPC cases and 1979 cancer-free controls. We found that the rs28362491 insATTG variants (ins/del + ins/ins) in NFB1 conferred an increased risk of NPC (odds ratio [ OR ] = 1.30, 95% confidence interval [ CI ] = 1.09 -1.55, and P = 2.80 × 10 - 3) compared with the del/del homozygous genotype. The rs696AA variant in IBα had an increased risk of NPC (OR = 1. 41, 95% CI = 1.20 -1.66, and P = 2.28 × 10 - 5) by decreasing IBα expression due to the modulation of microRNA hsa-miR-449a. Furthermore, both adverse genotypes of NFB/IBα and their interaction also exerted an increased risk on NPC. Taken together, Our findings indicated that genetic variants in NFB1 (rs28362491del> A) and their synergistic effect might contribute to NPC predisposition.