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PDCD6基因变异与肺癌易感性

Genetic variation in PDCD6 and susceptibility to lung cancer.

作者信息

He Yan-Qi, Zhou Bin, Shi Shao-Qing, Zhang Lin, Li Wei-Min

机构信息

Department of Respiratory Medicine, West China Hospital of Sichuan University, China.

出版信息

Asian Pac J Cancer Prev. 2012;13(9):4689-93. doi: 10.7314/apjcp.2012.13.9.4689.

Abstract

Lung cancer is the most common type of cancer and one of the leading causes of death in the world. Genetic factors play an important role in its development. PDCD6, the encoding gene for programmed cell death protein 6, may function as a tumor suppressor gene. Non-small cell lung cancer (NSCLC) contributes about 80% to newly histologically diagnosed lung cancer patients. To explore the relationship between PDCD6 and NSCLC, we examined two single nucleotide polymorphisms(rs3756712 G/T andrs4957014 G/T, both in the intron region) of the PDCD6gene.A hospital-based case-control study was carried out including 302 unrelated NSCLC patients and 306 healthy unrelated subjects. Significantly increased NSCLC risk was found to be associated with the T allele of rs4957014 (P=0.027, OR=0.760, 95%CI=0.596-0.970). The genotype and allele frequencies of rs3756712 did not shown any significant difference between NSCLC group and controls (P=0.327, OR=0.879, 95%CI=0.679- 1.137). In conclusion, we firstly demonstrated the association between the PDCD6 gene and risk of NSCLC in a Chinese Han population.

摘要

肺癌是最常见的癌症类型之一,也是全球主要的死亡原因之一。遗传因素在其发展过程中起着重要作用。程序性细胞死亡蛋白6的编码基因PDCD6可能作为一种肿瘤抑制基因发挥作用。非小细胞肺癌(NSCLC)约占新组织学诊断肺癌患者的80%。为了探讨PDCD6与NSCLC之间的关系,我们检测了PDCD6基因的两个单核苷酸多态性(rs3756712 G/T和rs4957014 G/T,均在内含子区域)。开展了一项基于医院的病例对照研究,纳入302例无亲缘关系的NSCLC患者和306名无亲缘关系的健康受试者。发现rs4957014的T等位基因与NSCLC风险显著增加相关(P = 0.027,OR = 0.760,95%CI = 0.596 - 0.970)。rs3756712的基因型和等位基因频率在NSCLC组和对照组之间未显示出任何显著差异(P = 0.327,OR = 0.879,95%CI = 0.679 - 1.137)。总之,我们首次在中国汉族人群中证明了PDCD6基因与NSCLC风险之间的关联。

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