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Association between single nucleotide polymorphisms on chromosome 17q and the risk of prostate cancer in a Chinese population

机译:中国人口17q染色体单核苷酸多态性与前列腺癌风险的关系

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摘要

In European populations,7 single nucleotide polymorphisms(SNPs) on chromosome 17q,3 SNPs on 17812,and 4 SNPs on 17824.3 were recently identified to be closely related to the risk of prostate cancer by a genome-wide association study.In Japanese populations,the correlation between 2 SNPs on 17q and the risk of prostate cancer and tumor aggressiveness was also confirmed by a large-scale experiment.However,whether 17q is associated with prostate cancer and its clinical manifestations in Chinese populations is still unknown.Therefore,we conducted a case-control study in a northern Chinese population and tested 2 SNPs,rs4430796 and rs1859962,on 17q in 124 prostate cancer patients and 111 controls using polymerase chain reaction-high resolution melting curve (PCR-HRM) combined with sequencing.We analyzed the association of the 2 SNPs with the risk of prostate cancer as well as patients'lifestyles,onset ages,Gleason scores,PSA levels,and pathologic stages.We found a significant difference in the G allele of SNP rs1859962(P=0.035,OR=1.51,95% CI=1.03-2.21) but not in the rs4430796 genotype frequency or allele frequency distribution between prostate cancer patients and the controls(P>0.05).Neither of the SNPs was significantly associated with the onset age,Gleason score,PSA level,pathologic stage,or other clinical indicators of patients with prostate cancer(P>0.05).Our results show that polymorphism of the G allele of SNP rs1859962 is associated with the risk of prostate cancer in a Chinese population.
机译:在欧洲群体中,在17812年的染色体17Q,3个SNP的7个单核苷酸多态性(SNP)和17824.3的4个SNPS在4824.3上鉴定到通过基因组的协会研究与前列腺癌的风险密切相关。在日本人口,通过大规模的实验,还证实了2季度2时SNP与前列腺癌和肿瘤侵略性的风险。然而,如果17Q与前列腺癌有关,中国人群的临床表现还是未知。因此,我们进行了北方北方人口和24例测试中的案例对照研究,在124例前列腺癌患者17 Q中进行了2个SNP,RS4430796和RS1859962,使用聚合酶链反应 - 高分辨率熔化曲线(PCR-HRM)与测序相结合的111例。我们分析了2个SNP与前列腺癌的风险以及患者的患者,发病年龄,GLEASON分数,PSA水平和病理阶段的风险。我们发现了显着差异SNP RS1859962的G等位基因(P = 0.035,或= 1.51,95%CI = 1.03-2.21),但不在Rs4430796基因型频率或前列腺癌患者和对照之间的等位基因分布(P> 0.05)。 SNP与前列腺癌患者的发病年龄,Gleason评分,PSA水平,病理阶段或其他临床指标有显着相关(P> 0.05)。SNP RS1859962的G等位基因的多态性与风险有关中国人口中的前列腺癌。

著录项

  • 来源
    《癌症(英文版)》 |2011年第010期|721-730|共10页
  • 作者单位

    The Fifth School of Clinical Medicine,Peking University,Beijing 100730,P.R.China;

    Department of Urology,Beijing Hospital,Ministry of Health,Beijing 100730,P.R.China;

    Beijing Institute of Geriatrics,Beijing Hospital,Ministry of Health,Beijing 100730,P.R.China;

    Department of Urology,Beijing Hospital,Ministry of Health,Beijing 100730,P.R.China;

    The Fifth School of Clinical Medicine,Peking University,Beijing 100730,P.R.China;

    Beijing Institute of Geriatrics,Beijing Hospital,Ministry of Health,Beijing 100730,P.R.China;

    Department of Urology,Beijing Hospital,Ministry of Health,Beijing 100730,P.R.China;

    Beijing Institute of Geriatrics,Beijing Hospital,Ministry of Health,Beijing 100730,P.R.China;

    Department of Urology,Beijing Hospital,Ministry of Health,Beijing 100730,P.R.China;

    Beijing Institute of Geriatrics,Beijing Hospital,Ministry of Health,Beijing 100730,P.R.China;

    Beijing Institute of Geriatrics,Beijing Hospital,Ministry of Health,Beijing 100730,P.R.China;

  • 收录信息 北京大学中文核心期刊目录(北大核心);中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类
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