Somatic mitochondrial DNA mutations in adult-onset leukaemia (original) (raw)
Anderson S, Bankier AT, Barrell BG, de Bruijn MH, Coulson AR, Drouin J et al. Sequence and organization of the human mitochondrial genome. Nature 1981; 290: 457–465. ArticleCAS Google Scholar
Yakes FM, Van Houten B . Mitochondrial DNA damage is more extensive and persists longer than nuclear DNA damage in human cells following oxidative stress. Proc Natl Acad Sci USA 1997; 94: 514–519. ArticleCAS Google Scholar
Marcelino LA, Thilly WG . Mitochondrial mutagenesis in human cells and tissues. Mutat Res 1999; 434: 177–203. ArticleCAS Google Scholar
Wallace DC . Mitochondrial diseases in man and mouse. Science 1999; 283: 1482–1488. ArticleCAS Google Scholar
DiMauro S, Schon EA . Mitochondrial DNA mutations in human disease. Am J Med Genet 2001; 106: 18–26. ArticleCAS Google Scholar
Chinnery PF, Johnson MA, Wardell TM, Singh-Kler R, Hayes C, Brown DT et al. Epidemiology of pathogenic mitochondrial DNA mutations. Ann Neurol 2000; 48: 188–193. ArticleCAS Google Scholar
Lightowlers RN, Chinnery PF, Turnbull DM, Howell N . Mammalian mitochondrial genetics: heredity, heteroplasmy and disease. Trends Genet 1997; 13: 450–455. ArticleCAS Google Scholar
McFarland R, Clark KM, Morris AA, Taylor RW, Macphail S, Lightowlers RN et al. Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation. Nat Genet 2002; 30: 145–146. ArticleCAS Google Scholar
Cortopassi G, Arnheim N . Detection of specific mitochondrial DNA deletion in tissues of older humans. Nucleic Acids Res 1990; 275: 169–180. Google Scholar
Wallace DC . Mitochondrial genetics: a paradigm for aging and degenerative diseases? Science 1992; 256: 628–632. ArticleCAS Google Scholar
Brierley EJ, Johnson MA, Lightowlers RN, James OF, Turnbull DM . Role of mitochondrial DNA mutations in human aging: implications for the central nervous system and muscle. Ann Neurol 1998; 43: 217–223. ArticleCAS Google Scholar
Kowald A, Kirkwood TB . Accumulation of defective mitochondria through delayed degradation of damaged organelles and its possible role in the ageing of post-mitotic and dividing cells. J Theor Biol 2000; 202: 145–160. ArticleCAS Google Scholar
Elson JL, Samuels DC, Turnbull DM, Chinnery PF . Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age. Am J Hum Genet 2001; 68: 802–806. ArticleCAS Google Scholar
Chinnery PF, Samuels DC, Elson J, Turnbull DM . Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism? Lancet 2002; 360: 1323–1325. ArticleCAS Google Scholar
Polyak K, Li Y, Zhu H, Lengauer C, Willson JK, Markowitz SD et al. Somatic mutations of the mitochondrial genome in human colorectal tumours. Nat Genet 1998; 20: 291–293. ArticleCAS Google Scholar
Augenlicht LH, Heerdt BG . Mitochondria: integrators in tumorigensis? Nat Genet 2001; 28: 104–105. ArticleCAS Google Scholar
Penta JS, Johnson FM, Wachsman JT, Copeland WC . Mitochondrial DNA in human malignancy. Mutat Res 2001; 488: 119–133. ArticleCAS Google Scholar
Fliss MS, Usadel H, Cabellero OL, Wu L, Buta MR, Eleff SM et al. Facile detection of mitochondrial DNA mutations in tumors and bodily fluids. Science 2000; 287: 2017–2019. ArticleCAS Google Scholar
Jeronimo C, Nomoto S, Caballero OL, Usadel H, Henrique R, Varzim G et al. Mitochondrial mutations in early stage prostate cancer and bodily fluids. Oncogene 2001; 20: 5195–5198. ArticleCAS Google Scholar
Jones JB, Song JJ, Hempen PM, Parmigiani G, Hruban RH, Kern SE . Detection of mitochondrial DNA mutations in pancreatic cancer offers a ‘mass’-ive advantage over detection of nuclear DNA mutations. Cancer Res 2001; 61: 1299–1304. CASPubMed Google Scholar
Kirches E, Krause G, Warich-Kirches M, Weis S, Schneider T, Meyer-Puttlitz B et al. High frequency of mitochondrial DNA mutations in glioblastoma multiforme identified by direct sequence comparison to blood samples. Int J Cancer 2001; 93: 534–538. ArticleCAS Google Scholar
Gattermann N, Retzlaff S, Wang Y-L, Berneburg M, Heinisch J, Wlaschek M et al. A heteroplasmic point mutation of mitochondrial tRNALeu(CUN) in non-lymphoid haemopoietic cell lineages from a patient with acquired idiopathic sideroblastic anaemia. Br J Haematol 1996; 93: 845–855. ArticleCAS Google Scholar
Gattermann N, Retzlaff S, Wang Y-L, Hofhaus G, Heinisch J, Aul C . Heteroplasmic point mutations of mitochondrial DNA affecting subunit I of cytochrome c oxidase in two patients with acquired idiopathic sideroblastic anemia. Blood 1997; 90: 4961–4972. CASPubMed Google Scholar
Wang YL, Choi HK, Aul C, Gattermann N, Heinisch J . The MERRF mutation of mitochondrial DNA in the bone marrow of a patient with acquired idiopathic sideroblastic anemia. Am J Hematol 1999; 60: 83–84. ArticleCAS Google Scholar
Greenberg PL, Young NS, Gattermann N . Myelodysplastic syndromes. Hematology (Am Soc Hematol Educ Program) 2002, 136–161.
Taylor RW, Taylor GA, Durham SE, Turnbull DM . The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations. Nucleic Acids Res 2001; 29: e74. ArticleCAS Google Scholar
Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, Howell N . Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat Genet 1999; 23: 147. ArticleCAS Google Scholar
Herrnstadt C, Elson JL, Fahy E, Preston G, Turnbull DM, Anderson C et al. Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups. Am J Hum Genet 2002; 70: 1152–1171. ArticleCAS Google Scholar
Wu CH, Yeh LS, Huang H, Arminski L, Castro-Alvear J, Chen Y et al. The protein information resource (PIR). Nucleic Acids Res 2003; 31: 345–347. Article Google Scholar
Ivanova R, Lepage V, Loste MN, Schachter F, Wijnen E, Busson M et al. Mitochondrial DNA sequence variation in human leukemic cells. Int J Cancer 1998; 76: 495–498. ArticleCAS Google Scholar
Reddy PL, Shetty VT, Dutt D, York A, Dar S, Mundle SD et al. Increased incidence of mitochondrial cytochrome _c_-oxidase gene mutations in patients with myelodysplastic syndromes. Br J Haematol 2002; 116: 564–575. ArticleCAS Google Scholar
Shin MG, Kajigaya S, Levin BC, Young NS . Mitochondrial DNA mutations in patients with myelodysplastic syndromes. Blood 2003; 101: 3118–3125. ArticleCAS Google Scholar
Broker S, Meunier B, Rich P, Gattermann N, Hofhaus G . MtDNA mutations associated with sideroblastic anaemia cause a defect of mitochondrial cytochrome c oxidase. Eur J Biochem 1998; 258: 132–138. ArticleCAS Google Scholar
Rötig A, Cormier V, Blanche S, Bonnefont J-P, Ledeist F . Pearson's marrow pancreas syndrome. A multisystem mitochondrial disorder of infancy. J Clin Invest 1990; 86: 1601–1608. Article Google Scholar