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作 者:曹凤军[1] 万国兴[1] 俞远东[1] 喻雄杰[1] 狄全书[1] 雷金华[1] 邓守恒[1] 陈萍[1]
机构地区:[1]湖北医药学院附属人民医院肿瘤科,十堰442000
出 处:《中华实验外科杂志》2015年第3期621-623,共3页Chinese Journal of Experimental Surgery
摘 要:目的 探讨瘦素(Leptin)基因-2 548 G/A多态性位点与非小细胞肺癌易感性及预后的关系.方法 采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术检测162例非小细胞肺癌和200例正常者的基因型,收集整理病例的临床病理及预后资料,并进行统计学分析.结果 瘦素基因-2 548 G/A位点实验组中AA、GA基因型及A等位基因频率(AA:35.2%;GA:46.3%;A:58.3%)均分别高于对照组(AA:16.5%;GA:40.0%;A:41.7%),差异有统计学意义[比值比(OR)=5.009,95%可信区间(CI):2.758 -9.097,P<0.01;OR=2.719,95% CI:1.615-4.578,P<0.01;OR=2.436,95% CI:1.804 - 3.289,P<0.01].Ⅲ+Ⅳ期的非小细胞肺癌中基因型为GA+AA的频率(58.3%)明显高于GG基因型(33.3%),同样在淋巴结转移患者中基因型为GA+ AA的频率(62.1%)明显高于GG基因型(40.0%),差异均有统计学意义(P<0.05).基因型为GA+ AA患者生存期[(37.7±1.1)个月]明显差于AA型患者[(45.9±2.9)个月],差异有统计学意义(x^2=8.215,P<0.01).结论 瘦素基因-2 548 G/A多态性可能与非小细胞肺癌易感性有关,并且可能是非小细胞肺癌的不良预后因子.Objective To explore the association of Leptin gene-2 548 G/A polymorphism with the susceptibility and prognosis of non-small cell lung cancer (NSCLC).Methods A total of 162 patients with NSCLC and 200 controls were enrolled in the case-control study.The genotypes were detected using reaction-restriction fragment length polymorphism (PCR-RFLP).Relevant clinicopathological data of selected cases were collected and analyzed.Results The frequencies of AA,GA and A allele in cases (AA:35.2 % ; GA:46.3 % ; A:58.3 %) were higher than that in controls (AA:16.5 % ; GA:40.0% ;A:41.7%),and significant differences were revealed [odds ratio (OR) =5.009,95% confidence interval (CI):2.758-9.097,P〈0.01;OR=2.719,95%CI:1.615-4.578,P〈0.01;OR=2.436,95%CI:1.804-3.289,P 〈 0.01],respectively.The frequencies of AA + GA genotype (58.3%) was found higher than GG genotype(33.3%) in NSCLC in Ⅲ + Ⅳ stage,likewise,the frequencies of AA + GA genotype(62.1%) were also found higher than GG genotype(40.0%) in NSCLC with lymph node metastasis,significant differences were also showed (both P 〈 0.05),and the survival of individuals carrying GA + AA (37.7 ± 1.1) genotype was markedly reduced compared to that carrying GG (45.9 ± 2.9) genotype (x2 =8.215,P 〈 0.01).Conclusion The present study suggests that the Leptin gene-2 548 G/A polymorphism may be associated with the susceptibility to NSCLC,and appear to jointly contribute to predicting a poor prognosis.
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