Nishikawa M, Nishiguchi S, Shiomi S, Tamori A, Koh N, Takeda T, Kubo S, Hirohashi K, Kinoshita H, Sato E, Inoue M
Department of Biochemistry, Osaka City University Medical School, Osaka, Japan.
Cancer Res. 2001 Mar 1;61(5):1843-5.
Unlike other types of cancer, hepatocellular carcinoma (HCC) is usually preceded by chronic inflammation caused by viral infection. The mutation of mitochondrial DNA (mtDNA) in hepatocarcinogenesis associated with viral infection was investigated. Compared with control liver tissue, the frequency of mtDNA mutations was markedly increased in both noncancerous and cancerous liver specimens from individuals with HCC. The accumulation of mtDNA mutations in HCC tissue reflected the degree of malignancy. The frequency of mtDNA mutations in HCC tissue was also greater than that described previously for other types of tumors. These observations suggest that the repeated destruction and regeneration of liver tissue associated with chronic viral hepatitis lead to the accumulation of mtDNA mutations. The genetic instability that results in the high rate of mtDNA mutation in cancerous liver tissue is also consistent with the multicentric hepatocarcinogenesis detected clinically.
与其他类型的癌症不同,肝细胞癌(HCC)通常由病毒感染引起的慢性炎症发展而来。研究了与病毒感染相关的肝癌发生过程中线粒体DNA(mtDNA)的突变情况。与对照肝脏组织相比,HCC患者的非癌性和癌性肝脏标本中mtDNA突变频率均显著增加。HCC组织中mtDNA突变的积累反映了恶性程度。HCC组织中mtDNA突变频率也高于先前报道的其他类型肿瘤。这些观察结果表明,与慢性病毒性肝炎相关的肝组织反复破坏和再生导致了mtDNA突变的积累。癌性肝组织中mtDNA高突变率所导致的遗传不稳定性也与临床检测到的多中心肝癌发生一致。