Yamashita Tomomi, Kato Keizo, Long Nguyen Khanh, Makita Hiroki, Yonemoto Kazuhiro, Iida Kazuki, Tamaoki Naritaka, Hatakeyama Daijiro, Shibata Toshiyuki
Department of Dentistry and Oral Surgery, Kouseiren Takaoka Hospital, Takaoka, Toyama 933-8555; ; Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Gifu University, Gifu, Gifu 501-1194, Japan.
Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Gifu University, Gifu, Gifu 501-1194, Japan.
Mol Clin Oncol. 2014 May;2(3):429-434. doi: 10.3892/mco.2014.267. Epub 2014 Mar 7.
Lifestyle, particularly smoking and alcohol consumption, may induce and/or inhibit drug metabolism. In order to reveal the effects of smoking and alcohol consumption on the 5-fluorouracil (5-FU)-related metabolic enzymes, namely thymidylate synthase, dihydropyrimidine dehydrogenase (DPD; a sole catabolic enzyme of 5-FU), orotate phosphoribosyl transferase (OPRT) and thymidine phosphorylase, in oral squamous cell carcinomas, the mRNA expression of these enzymes was investigated in 29 surgical specimens and compared by the Brinkman index and drinking years. The surgical specimens were divided into normal and tumor regions and were independently analyzed using quantitative reverse transcription-polymerase chain reaction. There was a significantly positive correlation between DPD mRNA expression in these tissues and Brinkman index/drinking years, with OPRT mRNA expression being significantly correlated to the Brinkman index in tumor tissues. These results revealed that lifestyle habits, including smoking and alcohol consumption, may vary the activity of the 5-FU-related metabolic enzymes. DPD is the initial and rate-limiting enzyme in the catabolic pathway of 5-FU. Therefore, smoking and alcohol consumption may reduce the anticancer activity of 5-FU, possibly through the induction of DPD activity.
生活方式,尤其是吸烟和饮酒,可能会诱导和/或抑制药物代谢。为了揭示吸烟和饮酒对口腔鳞状细胞癌中与5-氟尿嘧啶(5-FU)相关的代谢酶(即胸苷酸合成酶、二氢嘧啶脱氢酶(DPD;5-FU唯一的分解代谢酶)、乳清酸磷酸核糖基转移酶(OPRT)和胸苷磷酸化酶)的影响,在29份手术标本中研究了这些酶的mRNA表达,并通过 Brinkman 指数和饮酒年限进行比较。手术标本分为正常区域和肿瘤区域,并使用定量逆转录-聚合酶链反应进行独立分析。这些组织中DPD mRNA表达与Brinkman指数/饮酒年限之间存在显著正相关,肿瘤组织中OPRT mRNA表达与Brinkman指数显著相关。这些结果表明,包括吸烟和饮酒在内的生活习惯可能会改变与5-FU相关的代谢酶的活性。DPD是5-FU分解代谢途径中的初始限速酶。因此,吸烟和饮酒可能会降低5-FU的抗癌活性,可能是通过诱导DPD活性来实现的。