Exon1 and -116 C/G Promoter Polymorphism on the X-Box DNA Binding Protein- 1 Gene is not Associated with Breast Cancer among Jordanian Women

Alsheikh Hussein, Lulu H; Khalil, Ahmad M; Alghadi, Ahmad Y; Abu Alhaija, Abed Alkarem

doi:10.31557/APJCP.2019.20.9.2739

Exon1 and -116 C/G Promoter Polymorphism on the X-Box DNA Binding Protein- 1 Gene is not Associated with Breast Cancer among Jordanian Women

Document Type : Research Articles

Authors

Department of Biological Sciences, Yarmouk University, Irbid, Jordan.

10.31557/APJCP.2019.20.9.2739

Abstract

Background: Human X -box binding protein 1 (XBP1), a critical gene in the endoplasmic reticulum stress response, is
located on chromosome 22q12, which has been linked with the pathogenesis of many diseases, particularly cancers such
as breast cancer (BC). Single nucleotide polymorphisms (SNPs) in the XBP1 gene can alter structure and function of the
gene. In this study, polymorphism in the promoter region and exon1 of the gene XBP1 and its association with BC
in Jordanian women was investigated. Methods: Polymorphism in the promoter and exon1 of XBP1 was analyzed
in 100 subjects (controls: n=40; BC patients=60). −116 C/G SNP was genotyped by Polymerase Chain Reaction
(PCR)-sequence specific primer technique. The odd ratios (ORs) at 95% confidence intervals (CIs) were computed
to assess the strength of this association. Results: The three genotypes of the SNP (GG, GC, CC) and their allelic
frequencies have nonsignificant differences between patients and control group. It was noticed that the frequencies of
the mutant allele (G) were (75.8% versus 24.2%)) in the patients and control groups, respectively, while those of the
normal allele (C) were (67.5% versus 32.5%). XBP1 (-116 G→C) G allele did not show significant association with
BC risk (confidence interval = 0.3534- 1.2395, odds ratio = 0.6619, P= 0.197). Moreover, there were no significant
mutations in the XBP1 exon1 neither in BC subjects nor control subjects. Conclusions: This is the first study to evaluate
the effect of polymorphism in the promoter and exon1 of XBP1 gene in the pathogenesis of BC in Jordanian women.
The results do not support a role for polymorphism in development of BC and further studies with a larger sample size
and detailed data should be performed in other populations.

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