Abstract
The sodium iodide symporter (NIS) (solute carrier family 5; SLC5A), mediates the active transport of iodine anion (I-) into thyroid follicular cells to facilitate thyroid hormone biosynthesis. Considering its fundamental role in thyroid function, our objective in this study is to explore its potential involvement in the pathogenesis of differentiated thyroid cancer (DTC). Following a preliminary sequencing of the gene in a representative sample of the general population, five variants, (1) rs45602038, (2) rs4808708, (3) rs4808709, (4) rs7250346 and (5) rs12327843, were selected for a larger population-based association study consisting of 507 cases and 597 controls, of which only the rs45602038_TT [Odds ratio (95% confidence interval) = 1.90 (1.26-2.88); p = 0.0021 was associated with disease following adjustment for other confounders using the multivariate analysis. Furthermore, a 5-mer haplotype CGAGT constructed from the five studied SNPs conferred a significant risk (chi(2) = 10.98; p = 0.0009) for DTC. This association trickled down through shorter derivatives, with the 4-mer haplotype CGAG (chi(2) = 13.25; p = 0.0003) displaying the most significant association and the 3-mer GAG (chi(2) = 11.80; p = 0.0006) being equally strongly linked to the disease. Comparison of the flanking derivatives of the primary 5-mer haplotype also indicated that the 3-mer CGA (chi(2) = 4.04; p = 0.045) constructed from SNP block 1-3 was a lot weaker than that of the AGT (chi(2) = 6.73; p = 0.0095) constructed from the blocks 3-5 from the other end of the gene. Put together, these data implicate the three nucleotide changes at the rs4808708, rs4808709 and rs7250346 loci (blocks 2-4) as the core for this relationship. (C) 2015 Elsevier B.V. All rights reserved.