Department of Molecular Medicine, Institute of Experimental Medicine Research, Istanbul University, and Department of Thoracic Surgery, Yedikule Teaching Hospital for Chest Diseases and Thoracic Surgery, Vakif Gureba cad, Capa, 34093, Istanbul, Turkey.
Med Oncol. 2011 Dec;28(4):1436-40. doi: 10.1007/s12032-010-9627-8. Epub 2010 Jul 20.
In this study, we aimed to investigate a possible association of the COX-2 polymorphisms with the risk of developing lung carcinoma. COX-2 (-765G→C; -1195A→G) gene polymorphisms were performed by polymerase chain reaction (PCR) and restriction fragment length polymorphism in 118 healthy individuals and 231 patients with lung carcinoma. The present study was the first that addressed the role of the COX-2-765G→C and -1195A→G polymorphisms in lung carcinoma in Turkish population. In the present study, we found that the frequencies of GG, CC, and CG genotypes of COX-2-765G→C and AA, GG, and AG genotypes of -1195A→G in our control group were 0.22, 0.22, 0.55 and 0.59, 0.0, 0.40, respectively. These frequencies in patient group were 0.34, 0.07, 0.58 and 0.74, 0.04, 0.24, respectively. There were statistically significant differences in COX-2-765G→C (P=0.0002) and -1195A→G genotypes (P=0.007) between the controls and patients. We found that individuals carrying -765 GG genotype and -765 G allele of COX-2 or 1195 AA genotype of COX-2 and -765G: -1195A haplotype had an increased risk for the development of lung carcinoma. In contrast, individuals with -765 CC, -1195 AG genotypes and -1195 G allele of COX-2 seem to be protective from lung carcinoma. We suggest that the COX-2-765G→C and -1195A→G genotypes may be a risk factor for lung carcinoma.
在这项研究中,我们旨在探讨 COX-2 多态性与肺癌发生风险的可能关联。通过聚合酶链反应(PCR)和限制性片段长度多态性,在 118 名健康个体和 231 名肺癌患者中检测 COX-2(-765G→C;-1195A→G)基因多态性。本研究首次在土耳其人群中探讨了 COX-2-765G→C 和-1195A→G 多态性在肺癌中的作用。在本研究中,我们发现 COX-2-765G→C 中 GG、CC 和 CG 基因型和-1195A→G 中 AA、GG 和 AG 基因型在对照组中的频率分别为 0.22、0.22、0.55 和 0.59、0.0、0.40,而在患者组中的频率分别为 0.34、0.07、0.58 和 0.74、0.04、0.24。COX-2-765G→C(P=0.0002)和-1195A→G 基因型(P=0.007)在对照组和患者组之间存在统计学显著差异。我们发现,携带 COX-2-765G 等位基因 GG 基因型和-765G 等位基因、COX-2-1195A 等位基因 AA 基因型和-765G:-1195A 单倍型的个体患肺癌的风险增加。相比之下,携带 COX-2-765G 等位基因 CC、-1195A 等位基因 AG 基因型和-1195G 等位基因的个体似乎对肺癌具有保护作用。我们认为 COX-2-765G→C 和-1195A→G 基因型可能是肺癌的危险因素。