메뉴 건너뛰기




Volumn 11, Issue 9, 2003, Pages 671-678

Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage

Author keywords

Coronary artery disease; DNA damage; Folate; Homocysteine; Methionine synthase reductase; Methylenetetrahydrofolate reductase; Micronucleus test

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ADENINE; ALANINE; CYSTEINE; FOLIC ACID; GLUTAMIC ACID; GUANINE; HOMOCYSTEINE; METHIONINE SYNTHASE REDUCTASE; OXIDOREDUCTASE; THREONINE; UNCLASSIFIED DRUG;

EID: 0141590217     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201024     Document Type: Article
Times cited : (75)

References (46)
  • 1
    • 0028069519 scopus 로고
    • Chemical pathology of homocysteine. II. Carcinogenesis and homocysteine thiolactone metabolism
    • McCully KS: Chemical pathology of homocysteine. II. Carcinogenesis and homocysteine thiolactone metabolism. Ann Clin Lab Sci 1994; 24: 27-59.
    • (1994) Ann. Clin. Lab. Sci. , vol.24 , pp. 27-59
    • McCully, K.S.1
  • 2
    • 0033304841 scopus 로고    scopus 로고
    • Hyperhomocysteinemia and the endocrine system: Implications for atherosclerosis and thrombosis
    • Fonseca V, Guba SC, Fink LM: Hyperhomocysteinemia and the endocrine system: implications for atherosclerosis and thrombosis. Endocr Rev 1999; 20: 738-759.
    • (1999) Endocr. Rev. , vol.20 , pp. 738-759
    • Fonseca, V.1    Guba, S.C.2    Fink, L.M.3
  • 3
    • 0034021375 scopus 로고    scopus 로고
    • Vascular involvement in cognitive decline and dementia. Epidemiologic evidence from the Rotterdam Study and the Rotterdam Scan Study
    • Breteler MM: Vascular involvement in cognitive decline and dementia. Epidemiologic evidence from the Rotterdam Study and the Rotterdam Scan Study. Ann NY Acad Sci 2000; 903: 457-465.
    • (2000) Ann. NY. Acad. Sci. , vol.903 , pp. 457-465
    • Breteler, M.M.1
  • 4
    • 0034234789 scopus 로고    scopus 로고
    • Homocysteine, Alzheimer's disease, and cognitive function
    • Miller JW: Homocysteine, Alzheimer's disease, and cognitive function. Nutrition 2000; 16: 675-677.
    • (2000) Nutrition , vol.16 , pp. 675-677
    • Miller, J.W.1
  • 5
    • 0033988240 scopus 로고    scopus 로고
    • Role of amniotic fluid homocysteine level and of fetal 5,10-methylenetetrahydrafolate reductase genotype in the etiology of neural tube defects
    • Wenstrom KD, Johanning GL, Owen J, Johnston KE, Acton S, Tamura T: Role of amniotic fluid homocysteine level and of fetal 5,10-methylenetetrahydrafolate reductase genotype in the etiology of neural tube defects. Am J Med Genet 2000; 90: 12-16.
    • (2000) Am. J. Med. Genet. , vol.90 , pp. 12-16
    • Wenstrom, K.D.1    Johanning, G.L.2    Owen, J.3    Johnston, K.E.4    Acton, S.5    Tamura, T.6
  • 6
    • 0026034240 scopus 로고
    • Thermolabile methylenetetrahydrofolate reductase: An inherited risk factor for coronary artery disease
    • Kang SS, Wong PW, Susmano A, Sora J, Norusis M, Ruggie N: Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease. Am J Hum Genet 1991; 48: 536-545.
    • (1991) Am. J. Hum. Genet. , vol.48 , pp. 536-545
    • Kang, S.S.1    Wong, P.W.2    Susmano, A.3    Sora, J.4    Norusis, M.5    Ruggie, N.6
  • 7
    • 0029049553 scopus 로고
    • A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
    • Frosst P, Blom HJ, Milos R et al: A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995; 10: 111-113.
    • (1995) Nat. Genet. , vol.10 , pp. 111-113
    • Frosst, P.1    Blom, H.J.2    Milos, R.3
  • 8
    • 0030027668 scopus 로고    scopus 로고
    • Relation between folate status a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations
    • Jacques PF, Bostom AG, Williams RR et al: Relation between folate status a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations. Circulation 1996; 93: 7-9.
    • (1996) Circulation , vol.93 , pp. 7-9
    • Jacques, P.F.1    Bostom, A.G.2    Williams, R.R.3
  • 9
    • 0030934392 scopus 로고    scopus 로고
    • Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease
    • Christensen B, Frosst P, Lussier-Cacan S et al: Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease. Arterioscler Thromb Vasc Biol 1997; 17: 569-573.
    • (1997) Arterioscler. Thromb. Vasc. Biol. , vol.17 , pp. 569-573
    • Christensen, B.1    Frosst, P.2    Lussier-Cacan, S.3
  • 10
    • 0032497941 scopus 로고    scopus 로고
    • Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: The result of a meta-analysis
    • Brattstrom L, Wilcken DE, Ohrvik J, Brudin L: Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis. Circulation 1998; 98: 2520-2526.
    • (1998) Circulation , vol.98 , pp. 2520-2526
    • Brattstrom, L.1    Wilcken, D.E.2    Ohrvik, J.3    Brudin, L.4
  • 11
    • 0037316039 scopus 로고    scopus 로고
    • Methylentetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12 and DNA damage in coronary artery disease
    • Andreassi MG, Botto N, Cocci F et al: Methylentetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12 and DNA damage in coronary artery disease. Hum Genet 2003; 112: 171-177.
    • (2003) Hum. Genet. , vol.112 , pp. 171-177
    • Andreassi, M.G.1    Botto, N.2    Cocci, F.3
  • 12
    • 0031971515 scopus 로고    scopus 로고
    • A second common mutation in the methylenetetrahydrofolate reductase gene: An additional risk factor for neural-tube defects
    • van der Put NM, Gabreels F, Stevens EM et al: A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects. Am J Hum Genet 1998; 62: 1044-1051.
    • (1998) Am. J. Hum. Genet. , vol.62 , pp. 1044-1051
    • van der Put, N.M.1    Gabreels, F.2    Stevens, E.M.3
  • 13
    • 0031687887 scopus 로고    scopus 로고
    • A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity
    • Weisberg I, Tran P, Christensen B, Sibani S, Rozen R: A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Mol Genet Metab 1998; 64: 169-172.
    • (1998) Mol. Genet. Metab. , vol.64 , pp. 169-172
    • Weisberg, I.1    Tran, P.2    Christensen, B.3    Sibani, S.4    Rozen, R.5
  • 14
    • 0033623867 scopus 로고    scopus 로고
    • The effect of 677C→T and 1298A→C mutations on plasma homocysteine and 5,10-methylenetetrahydrofolate reductase activity in healthy subjects
    • Chango A, Boisson F, Barbe F et al: The effect of 677C→T and 1298A→C mutations on plasma homocysteine and 5,10-methylenetetrahydrofolate reductase activity in healthy subjects. Br J Nutr 2000; 83: 593-596.
    • (2000) Br. J. Nutr. , vol.83 , pp. 593-596
    • Chango, A.1    Boisson, F.2    Barbe, F.3
  • 15
    • 0035057410 scopus 로고    scopus 로고
    • C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: Incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease
    • Hanson NQ, Aras O, Yang F, Tsai MY: C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease. Clin Chem 2001; 47: 661-666.
    • (2001) Clin. Chem. , vol.47 , pp. 661-666
    • Hanson, N.Q.1    Aras, O.2    Yang, F.3    Tsai, M.Y.4
  • 16
    • 0036019532 scopus 로고    scopus 로고
    • A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: Relationships with C677T polymorphism and homocysteine/folate metabolism
    • Friso S, Girelli D, Trabetti E et al: A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolism. Clin Exp Med 2002; 2: 7-12.
    • (2002) Clin. Exp. Med. , vol.2 , pp. 7-12
    • Friso, S.1    Girelli, D.2    Trabetti, E.3
  • 17
    • 0032856882 scopus 로고    scopus 로고
    • A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida
    • Wilson A, Platt R, Wu Q et al: A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida. Mol Genet Metab 1999; 67: 317-323.
    • (1999) Mol. Genet. Metab. , vol.67 , pp. 317-323
    • Wilson, A.1    Platt, R.2    Wu, Q.3
  • 18
    • 0033846999 scopus 로고    scopus 로고
    • Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome
    • Hobbs CA, Sherman SL, Yi P et al: Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome. Am J Hum Genet 2000; 67: 623-630.
    • (2000) Am. J. Hum. Genet. , vol.67 , pp. 623-630
    • Hobbs, C.A.1    Sherman, S.L.2    Yi, P.3
  • 21
    • 0035958288 scopus 로고    scopus 로고
    • Evidence for DNA damage in patients with coronary artery disease
    • Botto N, Rizza A, Colombo MG et al: Evidence for DNA damage in patients with coronary artery disease. Mutat Res 2001; 493: 23-30.
    • (2001) Mutat. Res. , vol.493 , pp. 23-30
    • Botto, N.1    Rizza, A.2    Colombo, M.G.3
  • 22
    • 0034693730 scopus 로고    scopus 로고
    • The in vitro micronucleus technique
    • Fenech M. The in vitro micronucleus technique. Mutat Res 2000; 455: 81-95.
    • (2000) Mutat. Res. , vol.455 , pp. 81-95
    • Fenech, M.1
  • 23
    • 0031717255 scopus 로고    scopus 로고
    • Putative susceptibility markers of coronary artery disease: Association between VDR genotype, smoking, and aromatic DNA adduct levels in human right atrial tissue
    • Van Schooten FJ, Hirvonen A, Maas LM et al: Putative susceptibility markers of coronary artery disease: association between VDR genotype, smoking, and aromatic DNA adduct levels in human right atrial tissue. FASEB J 1998; 12: 1409-1417.
    • (1998) FASEB J. , vol.12 , pp. 1409-1417
    • Van Schooten, F.J.1    Hirvonen, A.2    Maas, L.M.3
  • 25
    • 0035499977 scopus 로고    scopus 로고
    • Association of plasma homocysteine with the number of major coronary arteries severely narrowed
    • Schnyder G, Pin R, Roffi M, Flammer Y, Hess OM: Association of plasma homocysteine with the number of major coronary arteries severely narrowed. Am J Cardiol 2001; 88: 1027-1030.
    • (2001) Am. J. Cardiol. , vol.88 , pp. 1027-1030
    • Schnyder, G.1    Pin, R.2    Roffi, M.3    Flammer, Y.4    Hess, O.M.5
  • 27
    • 0032865186 scopus 로고    scopus 로고
    • A common mutation A1298C in human methylenetetrahydrofolate reductase gene: Association with plasma total homocysteine and folate concentrations
    • Friedman G, Goldschmidt N, Friedlander Y et al: A common mutation A1298C in human methylenetetrahydrofolate reductase gene: association with plasma total homocysteine and folate concentrations. J Nutr 1999; 129: 1656-1661.
    • (1999) J. Nutr. , vol.129 , pp. 1656-1661
    • Friedman, G.1    Goldschmidt, N.2    Friedlander, Y.3
  • 28
    • 12444250748 scopus 로고    scopus 로고
    • Corrigendum to 'The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations'
    • (in press)
    • Gaughan DJ, Kluijtmans LA, Barbaux S et al: Corrigendum to 'The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations'. Atherosclerosis (in press).
    • Atherosclerosis
    • Gaughan, D.J.1    Kluijtmans, L.A.2    Barbaux, S.3
  • 29
    • 0033912873 scopus 로고    scopus 로고
    • A common polymorphism in methionine synthase reductase increases risk of premature coronary artery disease
    • Brown CA, McKinney KQ, Kaufman JS, Gravel RA, Rozen R: A common polymorphism in methionine synthase reductase increases risk of premature coronary artery disease. J Cardiovasc Risk 2000; 7: 197-200.
    • (2000) J. Cardiovasc. Risk , vol.7 , pp. 197-200
    • Brown, C.A.1    McKinney, K.Q.2    Kaufman, J.S.3    Gravel, R.A.4    Rozen, R.5
  • 30
    • 0034023742 scopus 로고    scopus 로고
    • Homocysteine and atherothrombosis - Mechanisms for injury
    • Thambyrajah J, Townend JN: Homocysteine and atherothrombosis - mechanisms for injury. Eur Heart J 2000; 21: 967-974.
    • (2000) Eur. Heart J. , vol.21 , pp. 967-974
    • Thambyrajah, J.1    Townend, J.N.2
  • 31
    • 0031410993 scopus 로고    scopus 로고
    • Folate, vitamin B12, homocysteine status and chromosome damage rate in lymphocytes of older men
    • Fenech MF, Dreosti IE, Rinaldi JR: Folate, vitamin B12, homocysteine status and chromosome damage rate in lymphocytes of older men. Carcinogenesis 1997; 18: 1329-1336.
    • (1997) Carcinogenesis , vol.18 , pp. 1329-1336
    • Fenech, M.F.1    Dreosti, I.E.2    Rinaldi, J.R.3
  • 32
    • 0031903189 scopus 로고    scopus 로고
    • Folate, vitamin, B12 homocysteine status and DNA damage in young Australian adults
    • Fenech M, Aitken C, Rinaldi J: Folate, vitamin, B12 homocysteine status and DNA damage in young Australian adults. Carcinogenesis 1998; 19: 1163-1171.
    • (1998) Carcinogenesis , vol.19 , pp. 1163-1171
    • Fenech, M.1    Aitken, C.2    Rinaldi, J.3
  • 33
    • 0034703084 scopus 로고    scopus 로고
    • Increase in plasma homocysteine associated with parallel increases in plasma S-adenosylhomocysteine and lymphocyte DNA hypomethylation
    • Yi P, Melnyk S, Pogribna M, Pogribny IP, Hine RJ, James SJ: Increase in plasma homocysteine associated with parallel increases in plasma S-adenosylhomocysteine and lymphocyte DNA hypomethylation. J Biol Chem 2000; 275: 29318-29323.
    • (2000) J. Biol. Chem. , vol.275 , pp. 29318-29323
    • Yi, P.1    Melnyk, S.2    Pogribna, M.3    Pogribny, I.P.4    Hine, R.J.5    James, S.J.6
  • 34
    • 0035010733 scopus 로고    scopus 로고
    • Preliminary study of the genotoxic potential of homocysteine in human lymphocytes in vitro
    • Crott J, Fenech M: Preliminary study of the genotoxic potential of homocysteine in human lymphocytes in vitro. Mutagenesis 2001; 16: 213-217.
    • (2001) Mutagenesis , vol.16 , pp. 213-217
    • Crott, J.1    Fenech, M.2
  • 35
    • 0035906327 scopus 로고    scopus 로고
    • The role of folic acid and Vitamin B12 in genomic stability of human cells
    • Fenech M: The role of folic acid and Vitamin B12 in genomic stability of human cells. Mutat Res 2001; 475: 57-67.
    • (2001) Mutat. Res. , vol.475 , pp. 57-67
    • Fenech, M.1
  • 38
    • 0036328453 scopus 로고    scopus 로고
    • Gene-nutrient interactions and DNA methylation
    • Friso S, Choi SW: Gene-nutrient interactions and DNA methylation. J Nutr 2002; 132: 2382S-2387S.
    • (2002) J. Nutr. , vol.132
    • Friso, S.1    Choi, S.W.2
  • 39
    • 0037221513 scopus 로고    scopus 로고
    • Coronary atherosclerosis and somatic mutations: An overview of the contributive factors for oxidative DNA damage
    • Andreassi MG: Coronary atherosclerosis and somatic mutations: an overview of the contributive factors for oxidative DNA damage. Mutat Res 2003; 543: 67-86.
    • (2003) Mutat. Res. , vol.543 , pp. 67-86
    • Andreassi, M.G.1
  • 40
    • 0030188563 scopus 로고    scopus 로고
    • The oxidant stress of hyperhomocyst(e)inemia
    • Loscalzo J: The oxidant stress of hyperhomocyst(e)inemia. J Clin Invest 1996; 98: 5-7.
    • (1996) J. Clin. Invest. , vol.98 , pp. 5-7
    • Loscalzo, J.1
  • 41
    • 0028242563 scopus 로고
    • Exclusion of specific human chromosomes into micronuclei by 5-azacytidine treatment of lymphocyte cultures
    • Guttenbach M, Schmid M: Exclusion of specific human chromosomes into micronuclei by 5-azacytidine treatment of lymphocyte cultures. Exp Cell Res 1994; 211: 127-132.
    • (1994) Exp. Cell Res. , vol.211 , pp. 127-132
    • Guttenbach, M.1    Schmid, M.2
  • 42
    • 0033547330 scopus 로고    scopus 로고
    • Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
    • Xu GL, Bestor TH Bourc'his D et al: Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene. Nature 1999; 402: 187-191.
    • (1999) Nature , vol.402 , pp. 187-191
    • Xu, G.L.1    Bestor, T.H.2    Bourc'his, D.3
  • 43
    • 0035989528 scopus 로고    scopus 로고
    • DNA hypomethylation and methyltransferase expression in atherosclerotic lesions
    • Hiltunen MO, Turunen MP, Hakkinen TP et al: DNA hypomethylation and methyltransferase expression in atherosclerotic lesions. Vasc Med 2002; 7: 5-11.
    • (2002) Vasc. Med. , vol.7 , pp. 5-11
    • Hiltunen, M.O.1    Turunen, M.P.2    Hakkinen, T.P.3
  • 45
    • 0033846460 scopus 로고    scopus 로고
    • Genomic DNA hypomethylation, a characteristic of most cancers, is present in peripheral leukocytes of individuals who are homozygous for the C677T polymorphism in the methylenetetrahydrofolate reductase gene
    • Stern LL, Mason JB, Selhub J, Choi SW: Genomic DNA hypomethylation, a characteristic of most cancers, is present in peripheral leukocytes of individuals who are homozygous for the C677T polymorphism in the methylenetetrahydrofolate reductase gene. Cancer Epidemiol Biomarkers Prev 2000; 9: 849-853.
    • (2000) Cancer Epidemiol. Biomarkers Prev. , vol.9 , pp. 849-853
    • Stern, L.L.1    Mason, J.B.2    Selhub, J.3    Choi, S.W.4
  • 46
    • 0037117501 scopus 로고    scopus 로고
    • A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status
    • Friso S, Choi SW, Girelli D et al: A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status. Proc Natl Acad Sci USA 2002; 99: 5606-5611.
    • (2002) Proc. Natl. Acad. Sci. USA , vol.99 , pp. 5606-5611
    • Friso, S.1    Choi, S.W.2    Girelli, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.