메뉴 건너뛰기




Volumn 3, Issue 5, 2010, Pages 741-747

Polymorphisms of 5,10-methylenetetrahydrofolate reductase and thymidylate synthase in squamous cell carcinoma and basal cell carcinoma of the skin

Author keywords

Basal cell carcinoma; Methylenetetrahydrofolate reductase; Skin; Squamous cell carcinoma; Thymidylate synthase

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); THYMIDYLATE SYNTHASE;

EID: 78049511246     PISSN: 17912997     EISSN: 17913004     Source Type: Journal    
DOI: 10.3892/mmr.2010.329     Document Type: Article
Times cited : (9)

References (37)
  • 1
    • 0036802287 scopus 로고    scopus 로고
    • Identification of 127 amino acid substitution variants in screening 37 DNA repair genes in humans
    • Mohrenweiser HW, Xi T, Vázquez-Matías J and Jones IM: Identification of 127 amino acid substitution variants in screening 37 DNA repair genes in humans. Cancer Epidemiol Biomarkers Prev 11: 1054-1064, 2002.
    • (2002) Cancer Epidemiol Biomarkers Prev , vol.11 , pp. 1054-1064
    • Mohrenweiser, H.W.1    Xi, T.2    Vázquez-Matías, J.3    Jones, I.M.4
  • 2
    • 0031428480 scopus 로고    scopus 로고
    • Presence and consequence of uracil in preneoplastic DNA from folate/methyl-deficient rats
    • Pogribny IP, Muskhelishvili L, Miller BJ and James SJ: Presence and consequence of uracil in preneoplastic DNA from folate/methyl-deficient rats. Carcinogenesis 18: 2071-2076, 1997.
    • (1997) Carcinogenesis , vol.18 , pp. 2071-2076
    • Pogribny, I.P.1    Muskhelishvili, L.2    Miller, B.J.3    James, S.J.4
  • 3
    • 0026064347 scopus 로고
    • Repair of uracil residues closely spaced on the opposite strands of plasmid DNA results in double strand break and deletion formation
    • Dianov GL, Timchenko TV, Sinitsina OI, Kuzminov AV, Medvedev OA and Salganik RI: Repair of uracil residues closely spaced on the opposite strands of plasmid DNA results in double strand break and deletion formation. Mol Gen Genet 225: 448-452, 1991.
    • (1991) Mol Gen Genet , vol.225 , pp. 448-452
    • Dianov, G.L.1    Timchenko, T.V.2    Sinitsina, O.I.3    Kuzminov, A.V.4    Medvedev, O.A.5    Salganik, R.I.6
  • 4
    • 0037377977 scopus 로고    scopus 로고
    • 5,10-methylenetetrahydrofolate reductase polymorphisms and leukemia risk: A HuGE minireview
    • Robien K and Ulrich CM: 5,10-methylenetetrahydrofolate reductase polymorphisms and leukemia risk: a HuGE minireview. Am J Epidemiol 157: 571-582, 2003.
    • (2003) Am J Epidemiol , vol.157 , pp. 571-582
    • Robien, K.1    Ulrich, C.M.2
  • 5
    • 0029049553 scopus 로고
    • A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
    • Frosst P, Blom HJ and Milos R: a candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10: 111-113, 1995.
    • (1995) Nat Genet , vol.10 , pp. 111-113
    • Frosst, P.1    Blom, H.J.2    Milos, R.3
  • 6
    • 0030811925 scopus 로고    scopus 로고
    • Genetic predisposition to hyperhomocysteinemia: Deficiency of methylenetetra hydrofolate reductase (MTHFR)
    • Rozen R: Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetra hydrofolate reductase (MTHFR). Thromb Haemost 78: 523-526, 1997.
    • (1997) Thromb Haemost , vol.78 , pp. 523-526
    • Rozen, R.1
  • 7
    • 0031687887 scopus 로고    scopus 로고
    • A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity
    • Weisberg I, Tran P, Chritensen B, Sibani S and Rozen R: A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Mol Genet Metab 64: 169-172, 1998.
    • (1998) Mol Genet Metab , vol.64 , pp. 169-172
    • Weisberg, I.1    Tran, P.2    Chritensen, B.3    Sibani, S.4    Rozen, R.5
  • 8
    • 0014545138 scopus 로고
    • Vascular pathology of homocysteinemia: Implication for the pathogenesis of arteriosclerosis
    • McCully KS: Vascular pathology of homocysteinemia: implication for the pathogenesis of arteriosclerosis. Am J Pathol 56: 111-128, 1969.
    • (1969) Am J Pathol , vol.56 , pp. 111-128
    • McCully, K.S.1
  • 9
  • 10
    • 0034617073 scopus 로고    scopus 로고
    • Homocysteine thiolactone and protein homocysteinylation in human endothelial cells: Implication for atherosclerosis
    • Jakubowski H, Zhang L, Bardequez A and Aviv A: Homocysteine thiolactone and protein homocysteinylation in human endothelial cells: implication for atherosclerosis. Circ Res 87: 45-47, 2000.
    • (2000) Circ Res , vol.87 , pp. 45-47
    • Jakubowski, H.1    Zhang, L.2    Bardequez, A.3    Aviv, A.4
  • 11
    • 29144468696 scopus 로고    scopus 로고
    • Association of methylenetetrahydrofolate reductase and thymidylate synthase promoter polymorphisms with genetic susceptibility to esophageal and cardia cancer in a Chinese high-risk population
    • Wang LD, Guo RF, Fan ZM, He X, Gao SS, Guo HQ, Matsuo K, Yin LM and Li JL: Association of methylenetetrahydrofolate reductase and thymidylate synthase promoter polymorphisms with genetic susceptibility to esophageal and cardia cancer in a Chinese high-risk population. Dis Esophagus 18: 177-184, 2005.
    • (2005) Dis Esophagus , vol.18 , pp. 177-184
    • Wang, L.D.1    Guo, R.F.2    Fan, Z.M.3    He, X.4    Gao, S.S.5    Guo, H.Q.6    Matsuo, K.7    Yin, L.M.8    Li, J.L.9
  • 12
    • 0035870245 scopus 로고    scopus 로고
    • Methylenetetrahydrofolate reductase polymorphisms increase risk of esophageal squamous cell carcinoma in a Chinese population
    • Song C, Xing D, Tan W, Wei Q and Lin D: Methylenetetrahydrofolate reductase polymorphisms increase risk of esophageal squamous cell carcinoma in a Chinese population. Cancer Res 61: 3272-3275, 2001. (Pubitemid 32695011)
    • (2001) Cancer Research , vol.61 , Issue.8 , pp. 3272-3275
    • Song, C.1    Xing, D.2    Tan, W.3    Wei, Q.4    Lin, D.5
  • 13
    • 0032799527 scopus 로고    scopus 로고
    • The 677C→T mutation in 5,10-methylenetetrahydrofolate reductase and colorectal cancer risk
    • Park KS, Mok JW and Kim JC: The 677C→T mutation in 5,10-methylenetetrahydrofolate reductase and colorectal cancer risk. Genet Test 3: 233-236, 1999.
    • (1999) Genet Test , vol.3 , pp. 233-236
    • Park, K.S.1    Mok, J.W.2    Kim, J.C.3
  • 15
    • 0023134446 scopus 로고
    • Role in translation of a triple tandemly repeated sequence in the 5'-untranslated region of human thymidylate synthase mRNA
    • Kaneda S, Takeishi K, Ayusawa D, Shimizu K, Seno T and Altman S: Role in translation of a triple tandemly repeated sequence in the 5′-untranslated region of human thymidylate synthase mRNA. Nucl Acids Res 15: 1259-1270, 1987. (Pubitemid 17012904)
    • (1987) Nucleic Acids Research , vol.15 , Issue.3 , pp. 1259-1270
    • Kaneda, S.1    Takeishi, K.2    Ayusawa, D.3
  • 16
    • 0021366060 scopus 로고
    • Chromosome breakage induced by thymidylate stress in thymidylate synthase-negative mutants of mouse FM3A cells
    • Hori T, Ayusawa D, Shimizu K, Koyama H and Seno T: Chromosome breakage induced by thymidylate stress in the thymidylate synthase-negative mutants of mouse FM3A cells. Cancer Res 44: 703-709, 1984. (Pubitemid 14184608)
    • (1984) Cancer Research , vol.44 , Issue.2 , pp. 703-709
    • Hori, T.1    Ayusawa, D.2    Shimizu, K.3
  • 17
    • 0032713838 scopus 로고    scopus 로고
    • Folic acid deficiency and cancer: Mechanisms of DNA instability
    • Duthie SJ: Folic acid deficiency and cancer: mechanisms of DNA instability. Br Med Bull 55: 578-592, 1999.
    • (1999) Br Med Bull , vol.55 , pp. 578-592
    • Duthie, S.J.1
  • 18
    • 0035093737 scopus 로고    scopus 로고
    • DNA double-strand breaks: Signaling, repair and the cancer connection
    • DOI 10.1038/85798
    • Khanna KK and Jackson SP: DNA double-strand breaks: signaling, repair and the cancer connection. Nat Genet 27: 247-254, 2001. (Pubitemid 32201842)
    • (2001) Nature Genetics , vol.27 , Issue.3 , pp. 247-254
    • Khanna, K.K.1    Jackson, S.P.2
  • 19
    • 0031824190 scopus 로고    scopus 로고
    • The human PTFgamma/SNAP43 gene: Structure, chromosomal location, and identification of a VNTR in 5′-UTR
    • Maeng JH and Yoon JB: The human PTFgamma/SNAP43 gene: structure, chromosomal location, and identification of a VNTR in 5′-UTR. J Biochem 14: 23-27, 1998.
    • (1998) J Biochem , vol.14 , pp. 23-27
    • Maeng, J.H.1    Yoon, J.B.2
  • 20
    • 0034771885 scopus 로고    scopus 로고
    • A novel single-nucleotide polymorphism in 3′-untranslated region of the human dihydrofolate reductase gene with enhanced expression
    • Goto Y, Yue L, Yokoi A, Nishimura R, Uehara T, Koizumi S and Saikawa Y: A novel single-nucleotide polymorphism in 3′-untranslated region of the human dihydrofolate reductase gene with enhanced expression. Clin Cancer Res 7: 1952-1956, 2001.
    • (2001) Clin Cancer Res , vol.7 , pp. 1952-1956
    • Goto, Y.1    Yue, L.2    Yokoi, A.3    Nishimura, R.4    Uehara, T.5    Koizumi, S.6    Saikawa, Y.7
  • 21
    • 0037045132 scopus 로고    scopus 로고
    • Expression of the dopamine transporter gene is regulated by the 3′ UTR VNTR: Evidence from brain and lymphocytes using quantitative RT-PCR
    • Mill J, Asherson P, Browes C, D'Souza U and Craig I: Expression of the dopamine transporter gene is regulated by the 3′ UTR VNTR: evidence from brain and lymphocytes using quantitative RT-PCR. Am J Med Genet 114: 975-979, 2002.
    • (2002) Am J Med Genet , vol.114 , pp. 975-979
    • Mill, J.1    Asherson, P.2    Browes, C.3    D'Souza, U.4    Craig, I.5
  • 22
    • 12344290346 scopus 로고    scopus 로고
    • Mechanisms of translational control by the 3′ UTR in development and differentiation
    • Moor CH, Meijer H and Lessenden S: Mechanisms of translational control by the 3′ UTR in development and differentiation. Semin Cell Dev Biol 16: 49-58, 2005.
    • (2005) Semin Cell Dev Biol , vol.16 , pp. 49-58
    • Moor, C.H.1    Meijer, H.2    Lessenden, S.3
  • 23
    • 0035430487 scopus 로고    scopus 로고
    • Polymorphism in the thymidylate synthase promoter enhancer region in colorectal cancer
    • Marsh S, McKay JA, Cassidy J and McLeod HL: Polymorphism in the thymidylate synthase promoter enhancer region in colorectal cancer. Int J Oncol 19: 383-386, 2001.
    • (2001) Int J Oncol , vol.19 , pp. 383-386
    • Marsh, S.1    McKay, J.A.2    Cassidy, J.3    McLeod, H.L.4
  • 24
    • 2442480694 scopus 로고    scopus 로고
    • A 6 bp polymorphism in the thymidylate synthase gene causes message instability and is associated with decreased intratumoral TS mRNA levels
    • DOI 10.1097/00008571-200405000-00007
    • Mandola MV, Stoehlmacher J, Zhang W, Groshen S, Yu MC, Iqbal S, Lens HJ and Ladner RD: A 6 bp polymorphism in the thymidylate syntase gene causes message instability and is associated with decreased intratumoral TS mRNA levels. Pharmacogenetics 14: 319-327, 2004. (Pubitemid 38638919)
    • (2004) Pharmacogenetics , vol.14 , Issue.5 , pp. 319-327
    • Mandola, M.V.1    Stoehlmacher, J.2    Zhang, W.3    Groshen, S.4    Yu, M.C.5    Iqbal, S.6    Lenz, H.-J.7    Ladner, R.D.8
  • 27
    • 0037096858 scopus 로고    scopus 로고
    • Thymidylate synthase promoter polymorphism, interaction with folate intake, and risk of colorectal adenomas
    • Ulrich CM, Bigler J, Bostrick R, Fosdick L and Potter JD: Thymidylate synthase promoter polymorphisms, interaction with folate intake, and risk of colorectal adenoma. Cancer Res 62: 3361-3364, 2002. (Pubitemid 34651378)
    • (2002) Cancer Research , vol.62 , Issue.12 , pp. 3361-3364
    • Ulrich, C.M.1    Bigler, J.2    Bostick, R.3    Fosdick, L.4    Potter, J.D.5
  • 29
    • 33847114380 scopus 로고    scopus 로고
    • Polymorphisms in thymidylate synthase gene and susceptibility to breast cancer in a Chinese population: A case-control analysis
    • Zhai X, Gao J, Hu Z, Tang J, Qin J and Wang S: Polymorphisms in thymidylate synthase gene and susceptibility to breast cancer in a Chinese population: a case-control analysis. BMC Cancer 6: 138, 2006.
    • (2006) BMC Cancer , vol.6 , pp. 138
    • Zhai, X.1    Gao, J.2    Hu, Z.3    Tang, J.4    Qin, J.5    Wang, S.6
  • 32
    • 0036141390 scopus 로고    scopus 로고
    • The XRCC1 Arg399Gln polymorphism, sunburn, and, non-melanoma skin cancer: Evidence of gene environment interaction
    • Nelson HH, Kelsey KT, Mott LA and Karagas MR: The XRCC1 Arg399Gln polymorphism, sunburn, and, non-melanoma skin cancer: evidence of gene environment interaction. Cancer Res 62: 152-155, 2002.
    • (2002) Cancer Res , vol.62 , pp. 152-155
    • Nelson, H.H.1    Kelsey, K.T.2    Mott, L.A.3    Karagas, M.R.4
  • 33
    • 0034980986 scopus 로고    scopus 로고
    • Polymorphisms of the DNA repair gene XPD: Correlations with risk of basal cell carcinoma revisited
    • Vogel U, Hedayati M, Dybdahl M, Grossman L and Nexo BA: Polymorphisms of the DNA repair gene XPD: correlations with risk of basal cell carcinoma revisited. Carcinogenesis 22: 899-904, 2001.
    • (2001) Carcinogenesis , vol.22 , pp. 899-904
    • Vogel, U.1    Hedayati, M.2    Dybdahl, M.3    Grossman, L.4    Nexo, B.A.5
  • 35
    • 1542394943 scopus 로고    scopus 로고
    • Use of pyrosequencing to detect clinically relevant polymorphisms of genes in basal cell carcinoma
    • Zhang Z, Liu W, Jia X, Gao Y, Hemminki K and Lindholm B: Use of pyrosequencing to detect clinically relevant polymorphisms of genes in basal cell carcinoma. Clin Chim Acta 342: 137-143, 2004.
    • (2004) Clin Chim Acta , vol.342 , pp. 137-143
    • Zhang, Z.1    Liu, W.2    Jia, X.3    Gao, Y.4    Hemminki, K.5    Lindholm, B.6
  • 37
    • 10344256121 scopus 로고    scopus 로고
    • Association of the thymidylate synthase polymorphisms with esophageal squamous cell carcinoma and gastric cardiac adenocarcinoma
    • DOI 10.1093/carcin/bgh247
    • Zhang J, Cui Y, Kuang G, Li Y, Wang N, Wang R, Guo W, Wen D, Wei L, Yu F and Wang S: Association of the thymidylate synthase polymorphisms with esophageal squamous cell carcinoma and gastric cardiac adenomacarcinoma. Carcinogenesis 25: 2479-2485, 2004. (Pubitemid 39625190)
    • (2004) Carcinogenesis , vol.25 , Issue.12 , pp. 2479-2485
    • Zhang, J.1    Cui, Y.2    Kuang, G.3    Li, Y.4    Wang, N.5    Wang, R.6    Guo, W.7    Wen, D.8    Wei, L.9    Yu, F.10    Wang, S.11


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.