Impairment of aldehyde dehydrogenase 2 increases accumulation of acetaldehyde-derived DNA damage in the esophagus after ethanol ingestion

American Journal of Cancer Research

Shinya Ohashi¹  Osamu Kikuchi¹  Manabu Muto¹  Mihoko Tsurumaki¹  Tomonari Matsuda¹  Tsutomu Chiba¹  Tsunehiro Oyama¹  Yukie Nakai¹  Shin’ichi Miyamoto¹  Toshihiro Kawamoto¹  Yoshiyuki Yukawa¹  Yusuke Amanuma¹ 

关键词: Carcinogenesis;    esophageal squamous cell carcinoma;    acetaldehyde;    acetaldehyde-derived DNA damage;    DNA adduct;   

DOI  :  

学科分类：肿瘤学

来源: e-Century Publishing Corporation

【 摘 要 】

Ethanol and its metabolite, acetaldehyde, are the definite carcinogens for esophageal squamous cell carcinoma (ESCC), and reduced catalytic activity of aldehyde dehydrogenase 2 (ALDH2), which detoxifies acetaldehyde, increases the risk for ESCC. However, it remains unknown whether the ALDH2 genotype influences the level of acetaldehyde-derived DNA damage in the esophagus after ethanol ingestion. In the present study, we administered ethanol orally or intraperitoneally to Aldh2-knockout and control mice, and we quantified the level of acetaldehyde-derived DNA damage, especially N²-ethylidene-2’-deoxyguanosine (N²-ethylidene-dG), in the esophagus. In the model of oral ethanol administration, the esophageal N²-ethylidene-dG level was significantly higher in Aldh2-knockout mice compared with control mice. Similarly, in the model of intraperitoneal ethanol administration, in which the esophagus is not exposed directly to the alcohol solution, the esophageal N²-ethylidene-dG level was also elevated in Aldh2-knockout mice. This result indicates that circulating ethanol-derived acetaldehyde causes esophageal DNA damage, and that the extent of damage is influenced by knockout of Aldh2. Taken together, our findings strongly suggest the importance of acetaldehyde-derived DNA damage which is induced in the esophagus of individuals with ALDH2 gene impairment. This provides a physiological basis for understanding alcohol-related esophageal carcinogenesis.

【 授权许可】

Unknown