Hiyama Toru, Tanaka Shinji, Shima Hideyuki, Kose Kazuhiro, Tuncel Handan, Ito Masanori, Kitadai Yasuhiko, Sumii Masaharu, Yoshihara Masaharu, Shimamoto Fumio, Haruma Ken, Chayama Kazuaki
Health Service Center, Hiroshima University, Higashihiroshima 739-8521, Japan.
Oncol Rep. 2003 Nov-Dec;10(6):1837-41.
It was reported that somatic mutations in the mitochondrial DNA (mtDNA) are associated with high-frequency microsatellite instability (MSI-H) of the nuclear in gastric cancers. However, no correlation between mtDNA mutations and nuclear MSI-H was found in colorectal, breast, and renal cancers. Therefore, the association between mtDNA mutations and nuclear MSI-H in gastric cancers is controversial. We examined mtDNA mutations and nuclear MSI in a large panel of gastric cancers. One-hundred and five gastric cancers were selected. Mutations in the mononucleotide repeat (D310) of mtDNA and nuclear MSI at 5 microsatellite loci were examined by microsatellite assay. Somatic mutations in the mtDNA and nuclear MSI-H were detected in 16 (15%) and 14 (13%) of the gastric cancers, respectively. mtDNA mutations were detected in 2 of the 14 (14%) and 14 of the 91 (15%) tumors with and without nuclear MSI-H, respectively. There was no significant difference between them. These results suggest that somatic mutations in the mtDNA and nuclear MSI-H play important roles in gastric carcinogenesis, and that mtDNA mutations may not be associated with nuclear MSI-H in gastric cancers.
据报道,线粒体DNA(mtDNA)中的体细胞突变与胃癌细胞核高频微卫星不稳定性(MSI-H)相关。然而,在结直肠癌、乳腺癌和肾癌中未发现mtDNA突变与细胞核MSI-H之间存在相关性。因此,mtDNA突变与胃癌细胞核MSI-H之间的关联存在争议。我们在大量胃癌样本中检测了mtDNA突变和细胞核MSI。选取了105例胃癌。通过微卫星分析检测了mtDNA单核苷酸重复序列(D310)中的突变以及5个微卫星位点的细胞核MSI。在16例(15%)和14例(13%)胃癌中分别检测到了mtDNA体细胞突变和细胞核MSI-H。在有和没有细胞核MSI-H的肿瘤中,分别有2例(14%)和14例(15%)检测到了mtDNA突变。两者之间无显著差异。这些结果表明,mtDNA体细胞突变和细胞核MSI-H在胃癌发生中起重要作用,并且mtDNA突变可能与胃癌细胞核MSI-H无关。