Kato S, Tajiri T, Matsukura N, Matsuda N, Taniai N, Mamada H, Yoshida H, Kiyam T, Naito Z
Surgery for Organ Function and Biological Regulation, Nippon Medical School, Tokyo, Japan.
Scand J Gastroenterol. 2003 Aug;38(8):886-93. doi: 10.1080/00365520310004489.
Hepatocellular carcinoma (HCC) in persons with liver cirrhosis (LC) arises following hepatitis virus infection. Alcohol may accelerate the risk of development of LC and HCC. Cytochrome p450 2E1 (CYP2E1) oxidizes ethanol to form acetaldehyde and aldehyde dehydrogenase 2 (ALDH2) detoxifies acetaldehyde, which is carcinogenic in humans, and both alcohol-metabolizing enzymes show the genetic polymorphisms in a Japanese population.
Using polymorphism analysis, we studied the frequency of ALDH2 functional deletion due to the G to A single-bp mutation in exon 12 and CYP2E1 polymorphism in the transcriptional region, both associated with higher levels of acetaldehyde, in 135 patients with LC and/or HCC, including 99 with HCC, and 135 non-cancer controls. The mRNA expression levels of CYP2E1 in the liver were also examined in 55 surgical specimens.
The allelic frequency of the homozygous ALDH2 2-2 genotype, coding for the enzyme deletion, was significantly higher compared to that of the homozygous or heterozygous ALDH2 1-1 genotypes in cases with HCC (OR = 5.4, 95% CI 2.1-14.0). There were no differences in the frequencies of specific genotypes of CYP2E1 in cases of HCC, but combined analysis of ALDH2 and CYP2E1 revealed that the odds ratio of occurrence of the C1/C1 homozygosity of CYP2E1 and the ALDH2 2-2 homozygosity was as high as 23.0 (2.9-182). The mRNA levels of CYP2E1 were higher in the liver of patients with the C1/C1 homozygosity of CYP2E1 than in those with other genotypes (P < 0.05).
ALDH2 and CYP2E1 polymorphisms may modify the risk of development of HCC against the background of LC in the Japanese. Polymorphism analysis of alcohol-metabolizing enzymes using molecular techniques may be useful in the risk assessment of liver cancer in patients with hepatitis C virus infection.
肝硬化(LC)患者的肝细胞癌(HCC)是在感染肝炎病毒后发生的。酒精可能会加速LC和HCC的发生风险。细胞色素P450 2E1(CYP2E1)将乙醇氧化形成乙醛,而乙醛脱氢酶2(ALDH2)可将具有致癌性的乙醛解毒,并且这两种酒精代谢酶在日本人群中均表现出基因多态性。
我们采用多态性分析,研究了135例LC和/或HCC患者(包括99例HCC患者)以及135例非癌症对照中,由于第12外显子中G到A单碱基突变导致的ALDH2功能缺失频率,以及转录区域中与乙醛水平升高相关的CYP2E1多态性。还对55份手术标本检测了肝脏中CYP2E1的mRNA表达水平。
编码酶缺失的纯合ALDH2 2-2基因型的等位基因频率,与HCC患者中的纯合或杂合ALDH2 1-1基因型相比显著更高(OR = 5.4,95% CI 2.1-14.0)。HCC病例中CYP2E1特定基因型的频率没有差异,但对ALDH2和CYP2E1的联合分析显示,CYP2E1的C1/C1纯合性和ALDH2 2-2纯合性同时出现的比值比高达23.0(2.9-182)。CYP2E1的C1/C1纯合性患者肝脏中的CYP2E1 mRNA水平高于其他基因型患者(P < 0.05)。
ALDH2和CYP2E1多态性可能会改变日本人群中LC背景下HCC的发生风险。使用分子技术对酒精代谢酶进行多态性分析,可能有助于评估丙型肝炎病毒感染患者的肝癌风险。