Copeland William C, Wachsman Joseph T, Johnson F M, Penta John S
Laboratory of Molecular Genetics, National Institute of Environmental Health Sciences, P.O. Box 12233, Research Triangle Park, NC 27709, USA.
Cancer Invest. 2002;20(4):557-69. doi: 10.1081/cnv-120002155.
A number of studies have demonstrated the presence of mitochondrial DNA (mtDNA) mutations in cancer cells. In this article, we review mitochondrial genomic aberrations reported in solid tumors of the breast, colon, stomach, liver, kidney, bladder, head/neck, and lung. The tantalizing association of tumors with mtDNA mutations implicates these mutations in the process of carcinogenesis. Alterations in expression of mtDNA transcripts in a variety of cancer types are also reviewed. In solid tumors, elevated expression of mtDNA-genes coding for subunits of the mitochondrial electron respiratory chain may reflect mitochondrial adaptation to perturbations in cellular energy requirements. The role of mtDNA mutations and altered expression of mitochondrial genes in carcinogenesis is discussed. Mitochondrial DNA mutations can initiate a cascade of events leading to a continuous increase in the production of reactive oxygen species (persistent oxidative stress), a condition that probably favors tumor development.
多项研究已证实癌细胞中存在线粒体DNA(mtDNA)突变。在本文中,我们综述了在乳腺癌、结肠癌、胃癌、肝癌、肾癌、膀胱癌、头颈部癌和肺癌等实体瘤中报道的线粒体基因组畸变。肿瘤与mtDNA突变之间诱人的关联表明这些突变参与了致癌过程。本文还综述了多种癌症类型中线粒体DNA转录本表达的改变。在实体瘤中,编码线粒体电子呼吸链亚基的mtDNA基因表达升高可能反映了线粒体对细胞能量需求扰动的适应性。本文讨论了mtDNA突变和线粒体基因表达改变在致癌过程中的作用。线粒体DNA突变可引发一系列事件,导致活性氧产生持续增加(持续性氧化应激),这种情况可能有利于肿瘤发展。