Mitochondrial haplogroup analysis in colorectal cancer: Identification of a high-risk population

Archives of Medical Science

Volumn 4, Issue 4, 2008, Pages 397-400

  Akouchekian, Mansoureh ^a,b,c   Houshmand, Massoud ^b,c  

^a LEIBNIZ UNIVERSITY HANNOVER   (Germany)

^b NATIONAL INSTITUTE OF GENETIC ENGINEERING AND BIOTECHNOLOGY   (Iran)

^c Special Medical Center Iran   (Iran)

Author keywords

Colorectal cancer; Haplogroup; Mitochondrial DNA

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; ARTICLE; CANCER RISK; CANCER SUSCEPTIBILITY; COLON CANCER; COLORECTAL CANCER; CONTROLLED STUDY; FEMALE; GENETIC ASSOCIATION; GENETIC RISK; HAPLOTYPE; HIGH RISK POPULATION; HUMAN; IRAN; MAJOR CLINICAL STUDY; MALE; SEQUENCE ANALYSIS;

EID: 60249091611     PISSN: 17341922     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (20)

1. Mishmar D, Ruiz-Pesini E, Golik P, et al. Natural selection shaped regional mtDNA variation in humans. Proc Natl Acad Sci USA 2003; 100: 171-6.
2. Wallace DC, Ruiz-Pesini E, Mishmar D. mtDNA variation, climatic adaptation, degenerative diseases, and longevity. Cold Spring Harb Symp Quant Biol 2003; 68: 479-86.
3. Ruiz-Pesini E, Mishmar D, Brandon M, Procaccio V, Wallace DC. Effects of purifying and adaptive selection on regional variation in human mtDNA. Science 2004; 303: 223-6.
4. Ozawa T, Tanaka M, Ino H, et al. Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease. Biochem Biophys Res Commun 1991; 176: 938-46.
5. Shoffner JM, Brown MD, Torroni A, et al. Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients. Genomics 1993; 17: 171-84.
6. Brown MD, Torroni A, Reckord CL, Wallace DC. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences. of the common mutations. Hum Mut 1995; 6: 311-25.
7. Torroni A, Petrozzi M, D'Urbano L, et al. Haplotype and phylogenetic analysis suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. Am J Hum Genet 1997; 60: 1107-21.
8. Fernández-Silva P, Enriquez JA, Montoya J. Replication and transcription of mammalian mitochondrial DNA. Exp Physiol 2003; 88: 41-56.
9. Suzuki M, Toyooka S, Miyajima K, et al. Alterations in the mitochondrial displacement loop in lung cancers. Clin Cancer Res 2003; 9: 5636-41.
10. Torroni A, Schurr TG, Cabell MF, et al. Asian affinities and continental radiation of the four founding Native American mtDNA. Am J Hum Genet 1993; 53: 563-90.
11. Graven L, Passarino G, Semino O, et al. Evolutionary correlation between control region sequence and restriction polymorphisms in the mitochondrial genome of a large Senegalese Mandenka population. Mol Biol Evol 1995; 12: 334-45.
12. Macaulay V, Richards M, Hickey E, et al. The emerging tree of West Eurasian mtDNAs: A synthesis of control-region sequences and RFLPs. Am J Hum Genet 1999; 64: 232-49.
13. Anderson S, Bankier AT, Barrel BG, et al. Sequence and organisation of the human mitochondrial genome. Nature 1981; 290: 457-64.
14. Torroni A, Huoponen K, Francalacci P, et al. Classification of European mtDNAs from an analysis of three European populations. Genetics 1996; 144: 1835-50.
15. Arnestad M, Opdal SH, Musse MA, Vege A, Rognum TO. Are substitutions in the first hypervariable region of mitochondrial DNA displacement-loop in sudden infant death syndrome due to maternal inheritance? Acta Paediatr 2002; 91: 1060-4.
16. Bai RK, Leal SM, Covarrubias D, Liu A, Wong LJ. Mitochondrial genetic background modifies breast cancer risk. Cancer Res 2007; 67: 4687-94.
17. Ghezzi D, Marelli C, Achilli A, et al. Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians. Eur J Hum Genet 2005; 13: 748-52.
18. Van der Walt JM, Nicodemus KK, Martin ER, et al. Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. Am J Hum Genet 2003; 72: 804-11.
19. Brown MD, Starikovskaya E, Derbeneva O, et al. The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J. Hum Genet 2002; 110: 130-8.
20. Hassani-Kumleh H, Houshmand M, Panahi MS, et al. Mitochondrial D-Loop variation in persian multiple sclerosis patients: K and A haplogroups as a rsk factor. Cell Mol Neu 2006; 26: 119-25.