| کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن | 
|---|---|---|---|---|
| 9110806 | 1568752 | 2005 | 4 صفحه PDF | دانلود رایگان | 
عنوان انگلیسی مقاله ISI
												Association of interleukin-1B (IL-1B) gene polymorphisms with risk of gastric cancer in Chinese population
												
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																																												موضوعات مرتبط
												
													علوم زیستی و بیوفناوری
													بیوشیمی، ژنتیک و زیست شناسی مولکولی
													علوم غدد
												
											پیش نمایش صفحه اول مقاله
												 
												چکیده انگلیسی
												The incidence of gastric cancer (GC) in China is among the highest in the world. In present work, 154 patients with GC and 166 healthy controls in population of north-western China were investigated to evaluate the genetic associations of IL-1B gene single nucleotide polymorphisms (SNP) and variable number tandem repeat (VNTR) polymorphisms of IL-1RN gene with increased risk of GC. The frequency of IL-1B+3954C/T was significantly higher in GC cases group (25.97%) than that in controls (4.82%) with odds ratio (OR) = 6.93 (95% confidence interval [CI] 3.13-15.36); the frequencies of IL-1B-31C/T, IL-1B-31C/C and IL-1B-511C/T genotypes were also higher in GC cases group (51.95%, 23.38% and 50.65%) than those in controls (46.99%, 19.88% and 42.77%) with OR = 1.48 (95% CI 0.88-2.49), OR = 1.58 (95% CI 0.84-2.95) and OR = 1.39 (95% CI 0.80-2.41), respectively. The results show that these SNPs of IL-1B gene are associated with significantly increased risk of GC. This is the first report that IL-1B+3954C/T heterozygote is associated with greatly increased risk of GC. The results of this study did not support the report that IL-1RN*2+ genotypes were associated with increased risk of GC in Chinese population.
											ناشر
												Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Cytokine - Volume 30, Issue 6, 21 June 2005, Pages 378-381
											Journal: Cytokine - Volume 30, Issue 6, 21 June 2005, Pages 378-381
نویسندگان
												Wei-Hua Zhang, Xun-Ling Wang, Jun Zhou, Li-Zhe An, Xiao-Dong Xie,