Habano W, Nakamura S, Sugai T
Division of Pathology, School of Medicine, Iwate Medical University, Uchimaru, Morioka, Japan.
Oncogene. 1998 Oct 15;17(15):1931-7. doi: 10.1038/sj.onc.1202112.
The role, if any, that mitochondrial (mt) DNA alterations play in the carcinogenic process remains unclear. To determine whether mtDNA instability occurs in cancers, nine microsatellite sequences in the mtDNA were examined in 45 sporadic colorectal carcinomas. Alteration in a polycytidine (C)n tract within a non-coding displacement-loop (D-loop) region was detected in 20 carcinomas (44%), three of which also exhibited frameshift mutations in a polyadenosine (A)8 or polycytidine (C)6 tract within NADH dehydrogenase (ND) genes. Interestingly, all three mutant genes were predicted to encode truncated ND proteins, which lacked a large portion of the C-terminus. These results suggested that certain repair systems, like the mismatch repair systems in the nuclear genome, are required for mtDNA maintenance and that defects in these systems can lead to target mitochondrial gene mutations in colorectal carcinomas.
线粒体(mt)DNA改变在致癌过程中所起的作用(如果有)仍不清楚。为了确定癌症中是否发生mtDNA不稳定性,我们在45例散发性结直肠癌中检测了mtDNA中的9个微卫星序列。在20例癌症(44%)中检测到非编码置换环(D环)区域内的聚胞苷(C)n序列改变,其中3例在NADH脱氢酶(ND)基因内的聚腺苷(A)8或聚胞苷(C)6序列中也表现出移码突变。有趣的是,所有三个突变基因预计编码截短的ND蛋白,这些蛋白缺少大部分C末端。这些结果表明,mtDNA的维持需要某些修复系统,如核基因组中的错配修复系统,并且这些系统的缺陷可导致结直肠癌中的靶线粒体基因突变。