کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5906371 | 1159970 | 2013 | 5 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Single nucleotide polymorphism in hMLH1 promoter and risk of tobacco-related oral carcinoma in high-risk Asian Indians
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کلمات کلیدی
UICCMutS homolog 2human MutL homolog 1NF-IL6BPDEhMLH1MSH2HNPCCMMROSCCDRCUnion for International Cancer Control - اتحادیه بین المللی کنترل سرطانbenzo(a)pyrene diol epoxide - بنزو (الف) پیروئید دیوال اپوکسیmismatch repair - تعمیر ناسازگاریPCR-RFLP - روش PCR-RFLPAsian Indians - سرخپوستان آسیاییOral cancer - سرطان دهانDNA repair capacity - ظرفیت تعمیر DNApolymerase chain reaction-restriction fragment length polymorphism - پلیمورفیسم طول قطعه واکنش زنجیره پلیمرازSingle nucleotide polymorphism - پلیمورفیسم تک نوکلئوتیدیSNP - چندریختی تک-نوکلئوتیدoral squamous cell carcinoma - کارسینوم سلول سنگفرشی دهانی
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
ژنتیک
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چکیده انگلیسی
hMLH1 is a member of mismatch repair genes (MMR) that plays a crucial role in correcting replication errors, cell cycle arrest, apoptosis and oxidative stress. We explored the risk associated with hMLH1 â 93 A>G (rs 1800734) single nucleotide polymorphism (SNP) with the oral squamous cell carcinoma (OSCC) in Asian Indians. We genotyped 242 patients with tobacco-related OSCC and 205 healthy controls by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique. The frequency of AA genotype was found to be significantly (Pc < 0.0006) lower in patients as compared to the controls (21.49% vs. 47.8%) while GG genotype showed significantly higher (Pc < 0.0006) prevalence in patients as compared to the healthy controls (41.32% vs. 13.66%). In logistic regression analysis AG (adjusted OR = 1.95, 95% CI = 0.72-5.26) and GG genotype (adjusted OR = 4.5, 95% CI = 1.54-13.16, P = 0.006) appeared susceptible when compared with the wild-type AA genotype. The allelic distribution showed that variant G allele is significantly higher (Pc < 0.0004) in patients and associated with increased risk (adjusted OR = 2.36, 95% CI = 1.33-4.19, P = 0.003) as compared to the wild-type A allele. Altogether, our results suggest that the hMLH1 â 93 A>G polymorphism is associated with the higher risk of tobacco-related OSCC in Asian Indians and could be useful in screening population at a higher risk.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gene - Volume 526, Issue 2, 10 September 2013, Pages 223-227
Journal: Gene - Volume 526, Issue 2, 10 September 2013, Pages 223-227
نویسندگان
Ritu Jha, Poonam Gaur, Suresh Chandra Sharma, Satya Narayan Das,