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Volumn 67, Issue 10, 2007, Pages 4687-4694

Mitochondrial genetic background modifies breast cancer risk

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

EID: 34250355048     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: 10.1158/0008-5472.CAN-06-3554     Document Type: Article
Times cited : (207)

References (49)
  • 1
    • 0035984912 scopus 로고    scopus 로고
    • ROS, stress-activated kinases and stress signaling in cancer
    • Benhar M, Engelberg D, Levitzki A. ROS, stress-activated kinases and stress signaling in cancer. EMBO Rep 2002;3:420-5.
    • (2002) EMBO Rep , vol.3 , pp. 420-425
    • Benhar, M.1    Engelberg, D.2    Levitzki, A.3
  • 2
    • 33746466098 scopus 로고    scopus 로고
    • Mitochondrial mutations in cancer
    • Brandon M, Baldi P, Wallace DC. Mitochondrial mutations in cancer. Oncogene 2006;25:4647-62.
    • (2006) Oncogene , vol.25 , pp. 4647-4662
    • Brandon, M.1    Baldi, P.2    Wallace, D.C.3
  • 3
    • 2642573655 scopus 로고    scopus 로고
    • Role of oxidative stress and the antioxidant network in cutaneous carcinogenesis
    • Sander CS, Chang H, Hamm F, Eisner P, Thiele JJ. Role of oxidative stress and the antioxidant network in cutaneous carcinogenesis. Int J Dermatol 2004;43:326-35.
    • (2004) Int J Dermatol , vol.43 , pp. 326-335
    • Sander, C.S.1    Chang, H.2    Hamm, F.3    Eisner, P.4    Thiele, J.J.5
  • 4
    • 0033083920 scopus 로고    scopus 로고
    • Manganese superoxide dismutase (MnSOD) genetic polymorphisms, dietary antioxidants, and risk of breast cancer
    • Ambrosone CB, Freudenheim JL, Thompson PA, et al. Manganese superoxide dismutase (MnSOD) genetic polymorphisms, dietary antioxidants, and risk of breast cancer. Cancer Res 1999;59:602-6.
    • (1999) Cancer Res , vol.59 , pp. 602-606
    • Ambrosone, C.B.1    Freudenheim, J.L.2    Thompson, P.A.3
  • 5
    • 0031736203 scopus 로고    scopus 로고
    • Somatic mutations of the mitochondrial genome in human colorectal tumours
    • Polyak K, Li Y, Zhu H, et al. Somatic mutations of the mitochondrial genome in human colorectal tumours. Nat Genet 1998;20:291-3.
    • (1998) Nat Genet , vol.20 , pp. 291-293
    • Polyak, K.1    Li, Y.2    Zhu, H.3
  • 6
    • 0036487995 scopus 로고    scopus 로고
    • The role of mtDNA background in disease expression: A new primary LHON mutation associated with Western Eurasian haplogroup
    • 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.
    • (2002) J. Hum Genet , vol.110 , pp. 130-138
    • Brown, M.D.1    Starikovskaya, E.2    Derbeneva, O.3
  • 7
    • 16944363113 scopus 로고    scopus 로고
    • Haplotype and phylogenetic analyses 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
    • Torroni A, Petrozzi M, D'Urbano L, et al. Haplotype and phylogenetic analyses 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.
    • (1997) Am J Hum Genet , vol.60 , pp. 1107-1121
    • Torroni, A.1    Petrozzi, M.2    D'Urbano, L.3
  • 8
    • 0037406049 scopus 로고    scopus 로고
    • Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction
    • Carelli V, Giordano C, d'Amati G. Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction. Trends Genet 2003;19:257-62.
    • (2003) Trends Genet , vol.19 , pp. 257-262
    • Carelli, V.1    Giordano, C.2    d'Amati, G.3
  • 9
    • 17744397107 scopus 로고    scopus 로고
    • Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease
    • Carrieri G, Bonafe M, De Luca M, et al. Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease. Hum Genet 2001;108:194-8.
    • (2001) Hum Genet , vol.108 , pp. 194-198
    • Carrieri, G.1    Bonafe, M.2    De Luca, M.3
  • 10
    • 0037241455 scopus 로고    scopus 로고
    • Mitochondrial 5178A/C genotype is associated with acute myocardial infarction
    • Mukae S, Aoki S, Itoh S, et al. Mitochondrial 5178A/C genotype is associated with acute myocardial infarction. Circ J 2003;67:16-20.
    • (2003) Circ J , vol.67 , pp. 16-20
    • Mukae, S.1    Aoki, S.2    Itoh, S.3
  • 11
    • 0035109413 scopus 로고    scopus 로고
    • Mitochondrial DNA polymorphisms in bipolar disorder
    • Kato T, Kunugi H, Nanko S, Kato N. Mitochondrial DNA polymorphisms in bipolar disorder. J Affect Disord 2001;62:151-64.
    • (2001) J Affect Disord , vol.62 , pp. 151-164
    • Kato, T.1    Kunugi, H.2    Nanko, S.3    Kato, N.4
  • 12
    • 0038308326 scopus 로고    scopus 로고
    • Phylogenetic assessment of the mitochondrial DNA displacement loop haplotype in Japanese patients with Leber's hereditary optic neuropathy harboring the mitochondrial DNA G11778A mutation
    • Isashiki Y, Sonoda S, Izumo S, Sakamoto T, Tachikui H, Inoue I. Phylogenetic assessment of the mitochondrial DNA displacement loop haplotype in Japanese patients with Leber's hereditary optic neuropathy harboring the mitochondrial DNA G11778A mutation. Ophthalmic Res 2003;35:224-31.
    • (2003) Ophthalmic Res , vol.35 , pp. 224-231
    • Isashiki, Y.1    Sonoda, S.2    Izumo, S.3    Sakamoto, T.4    Tachikui, H.5    Inoue, I.6
  • 13
    • 0034979652 scopus 로고    scopus 로고
    • Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln
    • Finnila S, Autere J, Lehtovirta M, et al. Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln. J Med Genet 2001;38:400-5.
    • (2001) J Med Genet , vol.38 , pp. 400-405
    • Finnila, S.1    Autere, J.2    Lehtovirta, M.3
  • 14
    • 0043066954 scopus 로고    scopus 로고
    • Increased variation in mtDNA in patients with familial sensorineural hearing impairment
    • Lehtonen MS, Moilanen JS, Majamaa K. Increased variation in mtDNA in patients with familial sensorineural hearing impairment. Hum Genet 2003;113:220-7.
    • (2003) Hum Genet , vol.113 , pp. 220-227
    • Lehtonen, M.S.1    Moilanen, J.S.2    Majamaa, K.3
  • 15
    • 2942750228 scopus 로고    scopus 로고
    • Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia
    • Autere J, Moilanen JS, Finnila S, et al. Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia. Hum Genet 2004;115:29-35.
    • (2004) Hum Genet , vol.115 , pp. 29-35
    • Autere, J.1    Moilanen, J.S.2    Finnila, S.3
  • 16
    • 20544461885 scopus 로고    scopus 로고
    • Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians
    • 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.
    • (2005) Eur J Hum Genet , vol.13 , pp. 748-752
    • Ghezzi, D.1    Marelli, C.2    Achilli, A.3
  • 17
    • 0037380725 scopus 로고    scopus 로고
    • mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish
    • Ross OA, McCormack R, Maxwell LD, et al. mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish. Exp Gerontol 2003;38:397-405.
    • (2003) Exp Gerontol , vol.38 , pp. 397-405
    • Ross, O.A.1    McCormack, R.2    Maxwell, L.D.3
  • 18
    • 0037385480 scopus 로고    scopus 로고
    • Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease
    • 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.
    • (2003) Am J Hum Genet , vol.72 , pp. 804-811
    • van der Walt, J.M.1    Nicodemus, K.K.2    Martin, E.R.3
  • 19
    • 0032497128 scopus 로고    scopus 로고
    • Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine
    • Majamaa K, Finnila S, Turkka J, Hassinen IE. Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine. Lancet 1998;352:455-6.
    • (1998) Lancet , vol.352 , pp. 455-456
    • Majamaa, K.1    Finnila, S.2    Turkka, J.3    Hassinen, I.E.4
  • 20
    • 0034676760 scopus 로고    scopus 로고
    • Increased risk of stroke in patients with the A12308G polymorphism in mitochondria
    • Pulkes T, Sweeney MG, Hanna MG. Increased risk of stroke in patients with the A12308G polymorphism in mitochondria. Lancet 2000;356:2068-9.
    • (2000) Lancet , vol.356 , pp. 2068-2069
    • Pulkes, T.1    Sweeney, M.G.2    Hanna, M.G.3
  • 22
    • 0031024138 scopus 로고    scopus 로고
    • Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes
    • Hofmann S, Bezold R, Jaksch M, et al. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes. Genomics 1997;39:8-18.
    • (1997) Genomics , vol.39 , pp. 8-18
    • Hofmann, S.1    Bezold, R.2    Jaksch, M.3
  • 23
    • 3042513691 scopus 로고    scopus 로고
    • Mitochondria dysfunction of Alzheimer's disease cybrids enhances Aβ toxicity
    • Cardoso SM, Santana I, Swerdlow RH, Oliveira CR. Mitochondria dysfunction of Alzheimer's disease cybrids enhances Aβ toxicity. J Neurochem 2004;89: 1417-26.
    • (2004) J Neurochem , vol.89 , pp. 1417-1426
    • Cardoso, S.M.1    Santana, I.2    Swerdlow, R.H.3    Oliveira, C.R.4
  • 24
    • 0031455734 scopus 로고    scopus 로고
    • Elevated reactive oxygen species and antioxidant enzyme activities in animal and cellular models of Parkinson's disease
    • Cassarino DS, Fall CP, Swerdlow RH, et al. Elevated reactive oxygen species and antioxidant enzyme activities in animal and cellular models of Parkinson's disease. Biochim Biophys Acta 1997;1362:77-86.
    • (1997) Biochim Biophys Acta , vol.1362 , pp. 77-86
    • Cassarino, D.S.1    Fall, C.P.2    Swerdlow, R.H.3
  • 25
    • 0029908226 scopus 로고    scopus 로고
    • Origin and functional consequences of the complex I defect in Parkinson's disease
    • Swerdlow RH, Parks JK, Miller SW, et al. Origin and functional consequences of the complex I defect in Parkinson's disease. Ann Neurol 1996;40:663-71.
    • (1996) Ann Neurol , vol.40 , pp. 663-671
    • Swerdlow, R.H.1    Parks, J.K.2    Miller, S.W.3
  • 26
    • 0028918334 scopus 로고
    • Superoxide and hydrogen peroxide in relation to mammalian cell proliferation
    • Burdon RH. Superoxide and hydrogen peroxide in relation to mammalian cell proliferation. Free Radic Biol Med 1995;18:775-94.
    • (1995) Free Radic Biol Med , vol.18 , pp. 775-794
    • Burdon, R.H.1
  • 27
    • 0035796023 scopus 로고    scopus 로고
    • The contribution of endogenous sources of DNA damage to the multiple mutations in cancer
    • Jackson AL, Loeb LA. The contribution of endogenous sources of DNA damage to the multiple mutations in cancer. Mutat Res 2001;477:7-21.
    • (2001) Mutat Res , vol.477 , pp. 7-21
    • Jackson, A.L.1    Loeb, L.A.2
  • 28
    • 0036832196 scopus 로고    scopus 로고
    • Oxidative stress, DNA damage, and breast cancer
    • Kang DH. Oxidative stress, DNA damage, and breast cancer. AACN Clin Issues 2002;13:540-9.
    • (2002) AACN Clin Issues , vol.13 , pp. 540-549
    • Kang, D.H.1
  • 29
    • 33746891176 scopus 로고    scopus 로고
    • Mitochondrial DNA mutations in human cancer
    • Chatterjee A, Mambo E, Sidransky D. Mitochondrial DNA mutations in human cancer. Oncogene 2006;25: 4663-74.
    • (2006) Oncogene , vol.25 , pp. 4663-4674
    • Chatterjee, A.1    Mambo, E.2    Sidransky, D.3
  • 30
    • 24744442376 scopus 로고    scopus 로고
    • Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women
    • Canter JA, Kallianpur AR, Parl FF, Millikan RC. Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women. Cancer Res 2005;65:8028-33.
    • (2005) Cancer Res , vol.65 , pp. 8028-8033
    • Canter, J.A.1    Kallianpur, A.R.2    Parl, F.F.3    Millikan, R.C.4
  • 31
    • 32944473298 scopus 로고    scopus 로고
    • Mims MP, Hayes TG, Zheng S, et al. Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women. Cancer Res 2006;66:1880; author reply -1.
    • Mims MP, Hayes TG, Zheng S, et al. Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women. Cancer Res 2006;66:1880; author reply -1.
  • 32
    • 1542293854 scopus 로고    scopus 로고
    • MtDNA evidence for a genetic bottleneck in the early history of the Ashkenazi Jewish population
    • Behar DM, Hammer MF, Garrigan D, et al. MtDNA evidence for a genetic bottleneck in the early history of the Ashkenazi Jewish population. Eur J Hum Genet 2004; 12:355-64.
    • (2004) Eur J Hum Genet , vol.12 , pp. 355-364
    • Behar, D.M.1    Hammer, M.F.2    Garrigan, D.3
  • 33
    • 0032486118 scopus 로고    scopus 로고
    • Yield of mtDNA mutation analysis in 2,000 patients
    • Liang MH, Wong LJ. Yield of mtDNA mutation analysis in 2,000 patients. Am J Med Genet 1998;77:395-400.
    • (1998) Am J Med Genet , vol.77 , pp. 395-400
    • Liang, M.H.1    Wong, L.J.2
  • 34
    • 0030850573 scopus 로고    scopus 로고
    • Direct detection of multiple point mutations in mitochondrial DNA
    • Wong LJ, Senadheera D. Direct detection of multiple point mutations in mitochondrial DNA. Clin Chem 1997; 43:1857-61.
    • (1997) Clin Chem , vol.43 , pp. 1857-1861
    • Wong, L.J.1    Senadheera, D.2
  • 35
    • 18344366125 scopus 로고    scopus 로고
    • Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups
    • Herrnstadt C, Elson JL, Fahy E, 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;70:1152-71.
    • (2002) Am J Hum Genet , vol.70 , pp. 1152-1171
    • Herrnstadt, C.1    Elson, J.L.2    Fahy, E.3
  • 36
    • 0033363826 scopus 로고    scopus 로고
    • The emerging tree of West Eurasian mtDNAs: A synthesis of control-region sequences and RFLPs
    • 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.
    • (1999) Am J Hum Genet , vol.64 , pp. 232-249
    • Macaulay, V.1    Richards, M.2    Hickey, E.3
  • 37
    • 0030468182 scopus 로고    scopus 로고
    • Classification of European mtDNAs from an analysis of three European populations
    • Torroni A, Huoponen K, Francalacci P, et al. Classification of European mtDNAs from an analysis of three European populations. Genetics 1996;144: 1835-50.
    • (1996) Genetics , vol.144 , pp. 1835-1850
    • Torroni, A.1    Huoponen, K.2    Francalacci, P.3
  • 38
    • 0013957190 scopus 로고
    • Combination of log relative risk in retrospective studies of disease
    • Sheehe PR. Combination of log relative risk in retrospective studies of disease. Am J Public Health Nations Health 1966;56:1745-50.
    • (1966) Am J Public Health Nations Health , vol.56 , pp. 1745-1750
    • Sheehe, P.R.1
  • 39
    • 0346373654 scopus 로고    scopus 로고
    • Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium
    • Carlson CS, Eberle MA, Rieder MJ, Yi Q, Kruglyak L, Nickerson DA. Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. Am J Hum Genet 2004; 74:106-20.
    • (2004) Am J Hum Genet , vol.74 , pp. 106-120
    • Carlson, C.S.1    Eberle, M.A.2    Rieder, M.J.3    Yi, Q.4    Kruglyak, L.5    Nickerson, D.A.6
  • 40
    • 13444269543 scopus 로고    scopus 로고
    • Haploview: Analysis and visualization of LD and haplotype maps
    • Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005;21:263-5.
    • (2005) Bioinformatics , vol.21 , pp. 263-265
    • Barrett, J.C.1    Fry, B.2    Maller, J.3    Daly, M.J.4
  • 41
    • 0032900678 scopus 로고    scopus 로고
    • Median-joining networks for inferring intraspecific phylogenies
    • Bandelt HJ, Forster P, Rohl A. Median-joining networks for inferring intraspecific phylogenies. Mol Biol Evol 1999;16:37-48.
    • (1999) Mol Biol Evol , vol.16 , pp. 37-48
    • Bandelt, H.J.1    Forster, P.2    Rohl, A.3
  • 42
    • 0033764821 scopus 로고    scopus 로고
    • Tracing European founder lineages in the Near Eastern mtDNA pool
    • Richards M, Macaulay V, Hickey E, et al. Tracing European founder lineages in the Near Eastern mtDNA pool. Am J Hum Genet 2000;67:1251-76.
    • (2000) Am J Hum Genet , vol.67 , pp. 1251-1276
    • Richards, M.1    Macaulay, V.2    Hickey, E.3
  • 43
    • 0027200741 scopus 로고
    • Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients
    • Shoffner JM, Brown MD, Torroni A, et al. Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients. Genomics 1993;17:171-84.
    • (1993) Genomics , vol.17 , pp. 171-184
    • Shoffner, J.M.1    Brown, M.D.2    Torroni, A.3
  • 44
    • 0037209210 scopus 로고    scopus 로고
    • Mitochondrial DNA polymorphisms associated with longevity in a Finnish population
    • Niemi AK, Hervonen A, Hurme M, Karhunen PJ, Jylha M, Majamaa K. Mitochondrial DNA polymorphisms associated with longevity in a Finnish population. Hum Genet 2003;112:29-33.
    • (2003) Hum Genet , vol.112 , pp. 29-33
    • Niemi, A.K.1    Hervonen, A.2    Hurme, M.3    Karhunen, P.J.4    Jylha, M.5    Majamaa, K.6
  • 45
    • 0028095263 scopus 로고
    • mtDNA and the origin of Caucasians: Identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region
    • Torroni A, Lott MT, Cabell MF, Chen YS, Lavergne L, Wallace DC. mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region. Am J Hum Genet 1994; 55:760-76.
    • (1994) Am J Hum Genet , vol.55 , pp. 760-776
    • Torroni, A.1    Lott, M.T.2    Cabell, M.F.3    Chen, Y.S.4    Lavergne, L.5    Wallace, D.C.6
  • 46
    • 0033525773 scopus 로고    scopus 로고
    • Mitochondrial diseases in man and mouse
    • Wallace DC. Mitochondrial diseases in man and mouse. Science 1999;283:1482-8.
    • (1999) Science , vol.283 , pp. 1482-1488
    • Wallace, D.C.1
  • 48
    • 0032851615 scopus 로고    scopus 로고
    • Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans
    • De Benedictis G, Rose G, Carrieri G, et al. Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans. FASEB J 1999;13:1532-6.
    • (1999) FASEB J , vol.13 , pp. 1532-1536
    • De Benedictis, G.1    Rose, G.2    Carrieri, G.3
  • 49
    • 30344471873 scopus 로고    scopus 로고
    • North American white mitochondrial haplogroups in prostate and renal cancer
    • discussion 72-3
    • Booker LM, Habermacher GM, Jessie BC, et al. North American white mitochondrial haplogroups in prostate and renal cancer. J Urol 2006;175:468-72; discussion 72-3.
    • (2006) J Urol , vol.175 , pp. 468-472
    • Booker, L.M.1    Habermacher, G.M.2    Jessie, B.C.3


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