Suzuki Takeshi, Matsuo Keitaro, Hasegawa Yasuhisa, Hiraki Akio, Wakai Kenji, Hirose Kaoru, Saito Toshiko, Sato Shigeki, Ueda Ryuzo, Tajima Kazuo
Division of Epidemiology and Prevention, Aichi Cancer Center Research Institute, 1-1 Kanokoden, Chikusa-ku, Nagoya 464-8681, Japan.
Cancer Sci. 2007 Sep;98(9):1439-46. doi: 10.1111/j.1349-7006.2007.00533.x. Epub 2007 Jun 26.
Low consumption of vegetables and fruits, which leads to insufficient folate intake, is associated with increased risk of several types of cancer, including head and neck squamous cell carcinoma (HNSCC). Functional polymorphisms in genes encoding one-carbon metabolism enzymes, such as methylenetetrahydrofolate reductase (MTHFR C677T and A1298C), methionine synthase (MTR A2756G), methionine synthase reductase (MTRR A66G) and thymidylate synthase (TS), influence folate metabolism and thus might impact on HNSCC risk. We conducted a case-control study with 237 HNSCC cases newly and histologically diagnosed and 711 age- and sex-matched non-cancer controls to clarify associations with these five polymorphisms. Gene-environment interactions between polymorphisms and smoking and drinking habit and folate consumption were also evaluated by logistic regression analysis. Dietary folate intake was inversely associated with HNSCC risk. None of the polymorphisms showed any significant impact on HNSCC risk by genotype alone, but we found interactions between drinking habit and MTHFR C667T (P = 0.04), MTR A2756G (P = 0.04) and MTRR A66G (P = 0.03) polymorphisms. The results suggest that there may be interactions between one-carbon metabolism-related polymorphisms and alcohol drinking for HNSCC risk.
蔬菜和水果摄入量低会导致叶酸摄入不足,这与包括头颈部鳞状细胞癌(HNSCC)在内的几种癌症风险增加有关。编码一碳代谢酶的基因中的功能多态性,如亚甲基四氢叶酸还原酶(MTHFR C677T和A1298C)、甲硫氨酸合成酶(MTR A2756G)、甲硫氨酸合成酶还原酶(MTRR A66G)和胸苷酸合成酶(TS),会影响叶酸代谢,因此可能会影响HNSCC风险。我们进行了一项病例对照研究,纳入237例新确诊且经组织学诊断的HNSCC病例以及711例年龄和性别匹配的非癌症对照,以阐明与这五种多态性的关联。还通过逻辑回归分析评估了多态性与吸烟、饮酒习惯以及叶酸摄入之间的基因-环境相互作用。膳食叶酸摄入量与HNSCC风险呈负相关。单独来看,这些多态性中没有一种对HNSCC风险有任何显著影响,但我们发现饮酒习惯与MTHFR C667T(P = 0.04)、MTR A2756G(P = 0.04)和MTRR A66G(P = 0.03)多态性之间存在相互作用。结果表明,一碳代谢相关多态性与饮酒之间可能存在相互作用,影响HNSCC风险。