p53 protein accumulation, cancer multiplicity, and aldehyde dehydrogenase-2 genotype in Japanese alcoholic men with early esophageal squamous cell carcinoma

被引:15
作者
Yokoyama, Akira
Omori, Tai
Tanaka, Yoichi
Yokoyama, Tetsuji
Sugiura, Hitoshi
Mizukami, Takeshi
Matsushita, Sachio
Higuchi, Susumu
Maruyama, Katsuya
Ishii, Hiromasa
Hibi, Toshifumi
机构
[1] Natl Hosp Org, Kurihama Alcoholism Ctr, Yokosuka, Kanagawa 2390841, Japan
[2] Kawasaki Municipal Hosp, Dept Gastroenterol, Kanagawa 2100013, Japan
[3] Kawasaki Municipal Hosp, Dept Surg, Kanagawa 2100013, Japan
[4] Ichikawa Gen Hosp, Tokyo Dent Coll, Dept Pathol, Chiba 2720824, Japan
[5] Kawasaki Municipal Hosp, Dept Pathol, Kanagawa 2100013, Japan
[6] Keio Univ, Sch Med, Dept Internal Med, Tokyo 1608582, Japan
关键词
esophageal cancer; p53; multiple cancer; aldehyde dehydrogenase-2; alcoholism;
D O I
10.1016/j.canlet.2006.05.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Synchronous multiple intra-esophageal squamous cell carcinomas (SCCs) or oropharyngolaryngeal SCCs are common in alcoholics with esophageal SCC, and more frequently found in those with inactive heterozygous aldehyde dehydrogenase-2 (ALDH2). p53 alterations have been suspected as key molecular events in such multifocal esophageal carcinogenesis. We studied 95 Japanese alcoholic men with Tis and mucosal invasive esophageal SCC and found very high levels of p53 protein accumulation occurring in early esophageal SCC. Synchronous cancer multiplicity in the upper aerodigestive tract was found in 40 patients. p53 expression was not correlated with either cancer multiplicity or ALDH2 genotype. The risk for cancer multiplicity was associated with inactive heterozygous ALDH2 alone (OR = 4.22) among the risk factors investigated, which also included smoking, less-active alcohol dehydrogenase-1B, and macrocytosis, enhancing the validity of the link between acetaldehyde exposure and cancer multiplicity. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:243 / 252
页数:10
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