Higuchi Masahiro
Department of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, 4301 West Markham, Slot 516 Little Rock, AR 72205-7199, USA.
Mitochondrion. 2007 Feb-Apr;7(1-2):53-7. doi: 10.1016/j.mito.2006.12.001. Epub 2006 Dec 5.
Enzymatic activities of the proteins encoded in nuclear genome are regulated by transcriptional, translational and post-transcriptional level. Enzymatic activities of proteins encoded in mitochondrial DNA (mtDNA) have been considered to be regulated by the same steps although detailed mechanisms might differ. However, dynamic change of the number of mtDNA, from some hundred to more than ten thousand, should be considered as another novel mechanism to regulate mtDNA-encoded proteins. Recently, we showed the connection of mtDNA depletion and deletion to cancer progression [Higuchi, M., Kudo, T., Suzuki, S., Evans, T.T., Sasaki, R., Wada, Y., Shirakawa, T., Sawyer, J.R., Gotoh, A., 2006. Mitochondrial DNA determines androgen dependence in prostate cancer cell lines. Oncogene 25, 1437-1445]. This review focuses and describes the possible connections of the mitochondrial DNA depletion and deletion to cancer.
核基因组中编码的蛋白质的酶活性受转录、翻译和转录后水平的调控。线粒体DNA(mtDNA)中编码的蛋白质的酶活性,尽管具体机制可能有所不同,但也被认为受相同步骤的调控。然而,mtDNA数量从几百到一万多个的动态变化,应被视为调控mtDNA编码蛋白质的另一种新机制。最近,我们发现mtDNA缺失与癌症进展之间的联系[Higuchi, M., Kudo, T., Suzuki, S., Evans, T.T., Sasaki, R., Wada, Y., Shirakawa, T., Sawyer, J.R., Gotoh, A., 2006. Mitochondrial DNA determines androgen dependence in prostate cancer cell lines. Oncogene 25, 1437 - 1445]。本综述重点关注并描述线粒体DNA缺失与癌症之间可能的联系。