Campa Daniele, Zienolddiny Shanbeh, Maggini Valentina, Skaug Vidar, Haugen Aage, Canzian Federico
Genome Analysis Group, International Agency for Research on Cancer, 150 Cours Albert Thomas, F-69372 Lyon Cedex 08, France.
Carcinogenesis. 2004 Feb;25(2):229-35. doi: 10.1093/carcin/bgh008. Epub 2003 Nov 6.
Studies have indicated that inflammation, in conjunction with the production of reactive oxygen species, may play a key role in lung cancer development. In this study, 250 lung cancer patients and 214 controls were genotyped for polymorphisms of the inflammation-related genes prostaglandin synthase-2/cyclooxygenase-2 (COX2/PTGS2), interleukin-6 (IL6), interleukin-8 (IL8) and peroxisome proliferator-activated receptor gamma (PPARg). We found that carriers of the C allele of a polymorphism in the 3'-UTR of COX2 had a significantly increased risk of lung cancer, with odds ratios of 4.28 (95% CI, 2.44-7.49) for homozygotes and 2.12 (95% CI, 1.25-3.59) for heterozygotes. Additionally, we found that an IL8 promoter polymorphism had a protective effect for lung cancer in female subjects, whereas an IL6 promoter polymorphism was only associated with risk of squamous cell carcinoma. This is the first study implicating polymorphisms in inflammatory genes in the risk of lung cancer.
研究表明,炎症与活性氧的产生共同作用,可能在肺癌发展中起关键作用。在本研究中,对250名肺癌患者和214名对照者进行了炎症相关基因前列腺素合成酶-2/环氧化酶-2(COX2/PTGS2)、白细胞介素-6(IL6)、白细胞介素-8(IL8)和过氧化物酶体增殖物激活受体γ(PPARg)多态性的基因分型。我们发现,COX2 3'-UTR区一个多态性的C等位基因携带者患肺癌的风险显著增加,纯合子的优势比为4.28(95%可信区间,2.44 - 7.49),杂合子为2.12(95%可信区间,1.25 - 3.59)。此外,我们发现IL8启动子多态性对女性肺癌有保护作用,而IL6启动子多态性仅与鳞状细胞癌风险相关。这是第一项表明炎症基因多态性与肺癌风险有关的研究。