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作 者:侯安继[1] 胡艳[1] 赵德民[2] 茅佩娟[3] 高红芳[1] 周莉[1]
机构地区:[1]上海市第七人民医院肿瘤科,上海200137 [2]上海市第七人民医院外科,上海200137 [3]上海市第七人民医院心内科,上海200137
出 处:《武汉大学学报(医学版)》2014年第4期560-564,共5页Medical Journal of Wuhan University
基 金:上海市卫生局资助项目(编号:20114196);上海市中医临床重点学科基金资助项目(编号:ZYXK2012010)
摘 要:目的:探讨血管紧张素转换酶(ACE)基因多态性在结直肠癌(CRC)发病中的作用。方法:入组120例CRC患者,采用聚合酶链反应(PCR)检测患者外周血中ACE基因多态性和等位基因分布频率,研究ACE基因缺失型(DD型)、II型和插入型(ID型)等3种基因型及I/D等位基因在CRC患者外周血中的分布频率,并与120例正常人检测结果进行对比。结果:CRC患者外周血标本中存在ACE基因插入/缺失(I/D)多态性分布,DD型、ID型和II型3种基因型的频率分别为15.00%,50.00%,35.00%,I/D等位基因分布频率分别为60.00%及40.00%;对照组的分布频率分别为16.67%,53.33%,30.00%,I/D等位基因分布频率分别为56.67%及43.33%,两组间3种基因型的分布频率无显著性差异(P>0.05)、I/D等位基因分布频率无显著差异(P>0.05)。分层分析表明,D等位基因变异与CRC低分化和远处转移相关(P<0.01及P<0.05)。结论:ACE基因I/D多态性与CRC存在一定关系,其中D等位基因异常与CRC低分化和易转移可能有关。Objective: To observe the correlation between the insertion/deletion (I/D) polymorphism of angiotensin Ⅰ-converting enzyme gene (ACE) and colorectal cancer (CRC). Methods: 120 CRC patients were enrolled in the study. Polymerase chain reaction (PCR) was served to detect insertion/deletion genotypes and I/D alleles of ACE gene in peripheral blood, and 120 volunteers served as control. Results: In CRC patients, the frequencies of genotypes of DD, ID and II of ACE gene were 15.00%, 50.00%, 35.00% respectively, I/D alleles frequencies were 60.00% and 40.00% respectively;in the control, the frequencies of genotypes of DD, ID and II of ACE gene were 16. 67%, 53. 33%, 30.00%, respectively, I/D alleles frequencies were 56. 67% and 43.33% respectively. The distribution of DD, ID and II genotypes of ACE gene and I/D alleles between the two groups showed no significant difference (P〉0.05). However, by stratification analyses, it was found that the change of D allele was correlated with poor differentiation and metastasis (P〈0.01 and P〈0.05). Conclusion : There was a correlation between ACE gene I/Dpolymorphism and CRC, and D allele might be a factor of poor differentiation and metastasis of CRC patients.
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