Lan Qing, Shen Min, Berndt Sonja I, Bonner Matthew R, He Xingzhou, Yeager Meredith, Welch Robert, Keohavong Phouthone, Donahue Mark, Hainaut Pierre, Chanock Stephen
Occupational and Environmental Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, MSC 7240, 6120 Executive Blvd., EPS 8109, Bethesda, MD 20892-7240, USA.
Lung Cancer. 2005 Sep;49(3):317-23. doi: 10.1016/j.lungcan.2005.04.004.
Lung cancer rates in Xuan Wei County are among the highest in China and have been associated with exposure to indoor smoky coal emissions that contain high levels of polycyclic aromatic hydrocarbons (PAHs). The NBS1 gene product participates in DNA double-strand break repair and DNA damage-induced checkpoint activation, which are critical for maintaining genomic integrity. The p53 tumor suppressor gene is known to play key roles both in the maintenance of genomic stability in mammalian cells and in DNA damage surveillance. We examined the association between two common NBS1 polymorphisms (Leu34Leu, Gln185Glu) and lung cancer risk in a population-based case-control study in Xuan Wei, China. Individuals homozygous for the NBS1 34Leu or NBS1 185Glu variants were found to have an increased risk of lung cancer (odds ratio [OR] 2.15, 95% confidence interval [CI]: 0.91-5.10 and OR 2.53, 95% CI: 1.05-6.08, respectively). A haplotype containing the variant alleles from both NBS1 SNPs was associated with increased risk of lung cancer compared with the most common haplotype. Further, the associations were particularly pronounced among cases with over expression of p53 protein. These results suggest that NBS1 could be important in the pathogenesis of lung cancer in this population. However, additional studies in other populations with substantial environmental exposures to PAHs are needed to confirm our findings.
宣威县的肺癌发病率位居中国前列,这与接触含有高浓度多环芳烃(PAHs)的室内燃煤烟雾有关。NBS1基因产物参与DNA双链断裂修复和DNA损伤诱导的检查点激活,这对于维持基因组完整性至关重要。已知p53肿瘤抑制基因在维持哺乳动物细胞基因组稳定性和DNA损伤监测中均发挥关键作用。我们在中国宣威进行了一项基于人群的病例对照研究,检测了两种常见的NBS1基因多态性(Leu34Leu、Gln185Glu)与肺癌风险之间的关联。结果发现,NBS1 34Leu或NBS1 185Glu变体的纯合个体患肺癌的风险增加(优势比[OR]分别为2.15,95%置信区间[CI]:0.91 - 5.10;以及OR 2.53,95% CI:1.05 - 6.08)。与最常见的单倍型相比,包含来自两个NBS1单核苷酸多态性的变异等位基因的单倍型与肺癌风险增加相关。此外,这些关联在p53蛋白过度表达的病例中尤为明显。这些结果表明,NBS1可能在该人群肺癌的发病机制中起重要作用。然而,需要在其他大量接触PAHs的人群中进行更多研究以证实我们的发现。