Yamamoto H, Tanaka M, Katayama M, Obayashi T, Nimura Y, Ozawa T
First Department of Surgery, Faculty of Medicine, University of Nagoya, Japan.
Biochem Biophys Res Commun. 1992 Jan 31;182(2):913-20. doi: 10.1016/0006-291x(92)91819-c.
To understand the role of mitochondria in carcinogenesis, we compared the amount of deleted mtDNAs between human hepatic tumors and surrounding cirrhotic portion of the liver of ten patients by using polymerase chain reaction (PCR). Multiple mtDNA deletions were detected in cirrhotic portion, but no deletions were detected in the tumor portion. Direct sequencing of the fragments revealed a 7,079-bp deletion (nucleotide position 8,992-16,072) involving no direct repeated sequences and a 7,436-bp deletion (position 8,649-16,084) involving a 12-bp directly repeated sequence of 5'-CATCAACAACCG-3' exists in both the ATP6 gene and the D-loop region. These mtDNA mutations could be one of the endogenous factors that induce somatic mutations in nuclear genome and etiologically contribute to human carcinogenesis.
为了解线粒体在致癌作用中的角色,我们运用聚合酶链反应(PCR)比较了10例患者的人类肝脏肿瘤与其周围肝硬化肝组织中缺失型线粒体DNA(mtDNA)的数量。在肝硬化组织中检测到多个mtDNA缺失,但在肿瘤组织中未检测到缺失。对片段进行直接测序发现,存在一个7079 bp的缺失(核苷酸位置8992 - 16072),该缺失不涉及直接重复序列;还有一个7436 bp的缺失(位置8649 - 16084),该缺失涉及ATP6基因和D环区域中一段5'-CATCAACAACCG-3'的12 bp直接重复序列。这些mtDNA突变可能是诱导核基因组发生体细胞突变并在病因学上导致人类致癌的内源性因素之一。