کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2815526 1159876 2015 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The potential role of the sodium iodide symporter gene polymorphism in the development of differentiated thyroid cancer
ترجمه فارسی عنوان
نقش بالقوه پلی مورفیسم ژن سیندرتر سدیم یتید سدیم در توسعه سرطان تیروئید متمایز
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی ژنتیک
چکیده انگلیسی


• We explore the role the NIS in differentiated thyroid cancer (DTC) in 507 cases and 597 controls.
• The rs45602038_C > T (p = 0.002) and haplotype CGAGT (χ2 = 10.98; p = 0.0009) conferred risk for DTC.
• Our data implicate changes at the rs4808708, rs4808709 and rs7250346 as the core for this relationship.

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 = 0.002] 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 (χ2 = 10.98; p = 0.0009) for DTC. This association trickled down through shorter derivatives, with the 4-mer haplotype CGAG (χ2 = 13.25; p = 0.0003) displaying the most significant association and the 3-mer GAG (χ2 = 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 (χ2 = 4.04; p = 0.045) constructed from SNP block 1–3 was a lot weaker than that of the AGT (χ2 = 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.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gene - Volume 572, Issue 2, 10 November 2015, Pages 163–168
نویسندگان
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