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作品数:2 被引量:5H指数:2
相关作者:朱龙彪袁华张宇陈宁更多>>
相关机构:南京医科大学更多>>
发文基金:国家教育部博士点基金国家自然科学基金江苏省自然科学基金更多>>
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let-7基因多态与中国汉族人群头颈癌易感性的关联研究被引量:3
2014年
目的:探讨 let-7基因多态与中国汉族人群头颈癌易感性的关联。方法:采用病例-对照研究设计,以经确诊的503例头颈部癌患者作为病例组,选取900例健康人群作为对照组。对病例-对照进行流行病学调查,内容包括:一般人口学特征、疾病史、肿瘤家族史、吸烟、饮酒情况,并进行体格检查。收集研究对象血液标本5 mL,提取基因组 DNA。以 let-7 rs10877887和rs13293512为研究位点,应用TaqMan探针方法进行多态性检测,并用logistic 回归计算比值比(odds ratio,OR)及其95%可信区间(confidence interval,CI),比较不同基因型与头颈癌患病风险的关系。结果:rs10877887位点3种基因型 TT、CT及 CC 在病例组分布频率分别为45.7%(227/503)、42.9%(213/503)及11.4%(57/503);在对照组中分别为40.8%(361/900)、47.7%(422/900)及11.5%(101/900)。rsl3293512位点3种基因型 TT、CT 及 CC 在病例组分布频率分别为31.9%(157/503)、52.3%(257/503)及15.8%(78/503),在对照组中分别为30.2%(270/900)、49.2%(439/900)及20.6%(194/900)。多因素 logistic 回归分析显示,携带 rs10877887位点至少1个突变等位基因 C 的个体与携带 TT基因型的个体相比,头颈部肿瘤患病风险差异无统计学意义(CC +CT/TT调整 OR=0.82,95% CI:0.90~1.23,P=0.087);与携带 TT+CT基因型个体相比较,携带 rs13293512位点2个突变等位基因 C 的个体头颈部肿瘤患病风险显著降低(CC/TT+CT 调整 OR=0.73,95% CI:0.55~0.98,P=0.039)。结论:let-7 rs13293512位点多态可影响中国汉族人群的罹患头颈癌的风险。
朱龙彪袁华张宇苗利民陈宁
关键词:LET-7头颈癌遗传易感性LET-7
Association of microRNA polymorphisms with the risk of head and neck squamous cell carcinoma in a Chinese population:a case-control study被引量:2
2016年
Background:MicroRNA(miRNA) polymorphisms may alter miRNA-related processes,and they likely contribute to cancer susceptibility.Various studies have investigated the associations between genetic variants in several key miRNAs and the risk of human cancers;however,few studies have focused on head and neck squamous cell carcinoma(HNSCC) risk.This study aimed to evaluate the associations between several key miRNA polymorphisms and HNSCC risk in a Chinese population.Methods:In this study,we genotyped five common single-nucleotide polymorphisms(SNPs) in several key miRNAs(miR-149 rs2292832,miR-146 a rs2910164,miR-605 rs2043556,miR-608 rs4919510,and miR-196a2 rs11614913) and evaluated the associations between these SNPs and HNSCC risk according to cancer site with a case-control study including 576 cases and 1552 controls,which were matched by age and sex in a Chinese population.Results:The results revealed that miR-605 rs2043556[dominant model:adjusted odds ratio(OR) 0.71,95%confidence interval(CI) 0.58-0.88;additive model:adjusted OR 0.74,95%CI 0.62-0.89]and miR-196a2 rs11614913(dominant model:adjusted OR 1.36,95%C11.08-1.72;additive model:adjusted OR 1.28,95%C11.10-1.48) were significantly associated with the risk of oral squamous cell carcinoma(OSCC).Furthermore,when these two loci were evaluated together based on the number of putative risk alleles(rs2043556 A and rs11614913 G),a significant locus-dosage effect was noted on the risk of OSCC(P_(trend) < 0.001).However,no significant association was detected between the other three SNPs(miR-149 rs2292832,miR- 146 a rs2910164,and miR-608 rs4919510) and HNSCC risk.Conclusion:Our study provided the evidence that miR-605 rs2043556 and miR-196a2 rs11614913 may have an impact on genetic susceptibility to OSCC in Chinese population.
Limin MiaoLihua WangLongbiao ZhuJiangbo DuXun ZhuYuming NiuRuixia WangZhibin HuNing ChenHongbing ShenHongxia Ma
关键词:MICRORNAPOLYMORPHISMSUSCEPTIBILITY
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