메뉴 건너뛰기




Volumn 48, Issue 12, 2009, Pages 1037-1050

Two candidate tumor suppressor genes, MEOX2 and SOSTDC1, identified in a 7p21 homozygous deletion region in a Wilms tumor

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; BISULFITE; LEUCINE; PHENYLALANINE;

EID: 70350247612     PISSN: 10452257     EISSN: 10982264     Source Type: Journal    
DOI: 10.1002/gcc.20705     Document Type: Article
Times cited : (31)

References (42)
  • 1
    • 0142027071 scopus 로고    scopus 로고
    • Derivation and characterization of a Wilms' tumour cell line, Wit 49
    • DOI 10.1002/ijc.11429
    • Alami J, Williams BR, Yeger H. 2003. Derivation and characterization of a Wilms' tumour cell line, WiT 49. Int J Cancer 107:365-374. (Pubitemid 37266455)
    • (2003) International Journal of Cancer , vol.107 , Issue.3 , pp. 365-374
    • Alami, J.1    Williams, B.R.2    Yeger, H.3
  • 2
    • 0018149630 scopus 로고
    • Histopathology and prognosis of Wilms tumor. Results from the first national Wilms' tumor study
    • DOI 10.1002/1097-0142(197805)41:5<1937::AID-CNCR2820410538>3.0. CO;2-U
    • Beckwith JB, Palmer NF. 1978. Histopathology and prognosis of Wilms tumor: Results from the First National Wilms' Tumor Study. Cancer 41:1937-1948. (Pubitemid 8335406)
    • (1978) Cancer , vol.41 , Issue.5 , pp. 1937-1948
    • Beckwith, J.B.1    Palmer, N.F.2
  • 4
    • 43049139864 scopus 로고    scopus 로고
    • Correlative gene expression and DNA methylation profiling in lung development nominate new biomarkers in lung cancer
    • Cortese R, Hartmann O, Berlin K, Eckhardt F. 2008. Correlative gene expression and DNA methylation profiling in lung development nominate new biomarkers in lung cancer. Int J Biochem Cell Biol 40:1494-1508.
    • (2008) Int J Biochem Cell Biol , vol.40 , pp. 1494-1508
    • Cortese, R.1    Hartmann, O.2    Berlin, K.3    Eckhardt, F.4
  • 6
    • 34548831074 scopus 로고    scopus 로고
    • Sequential WT1 and CTNNB1 mutations and alterations of β-catenin localization in intralobar nephrogenic rests and associated Wilms tumours: Two case studies
    • Fukuzawa R, Heathcott RW, More HE, Reeve AE. 2007. Sequential WT1 and CTNNB1 mutations and alterations of β-catenin localization in intralobar nephrogenic rests and associated Wilms tumours: Two case studies. J Clin Pathol 60:1013-1016.
    • (2007) J Clin Pathol , vol.60 , pp. 1013-1016
    • Fukuzawa, R.1    Heathcott, R.W.2    More, H.E.3    Reeve, A.E.4
  • 7
    • 61349113324 scopus 로고    scopus 로고
    • Canonical WNT signalling determines lineage specificity in Wilms tumour
    • Fukuzawa R, Anaka MR, Weeks RJ, Morison IM, Reeve AE. 2009. Canonical WNT signalling determines lineage specificity in Wilms tumour. Oncogene 28:1063-1075.
    • (2009) Oncogene , vol.28 , pp. 1063-1075
    • Fukuzawa, R.1    Anaka, M.R.2    Weeks, R.J.3    Morison, I.M.4    Reeve, A.E.5
  • 8
    • 0025098654 scopus 로고
    • Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping
    • DOI 10.1038/343774a0
    • Gessler M, Poustka A, Cavenee W, Neve RL, Orkin SH, Bruns GA. 1990. Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping. Nature 343:774-778. (Pubitemid 20065258)
    • (1990) Nature , vol.343 , Issue.6260 , pp. 774-778
    • Gessler, M.1    Poustka, A.2    Cavenee, W.3    Neve, R.L.4    Orkin, S.H.5    Bruns, G.A.P.6
  • 10
    • 0032560798 scopus 로고    scopus 로고
    • Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour
    • Grundy RG, Pritchard J, Scambler P, Cowell JK. 1998. Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour. Oncogene 17:395-400. (Pubitemid 28383016)
    • (1998) Oncogene , vol.17 , Issue.3 , pp. 395-400
    • Grundy, R.G.1    Pritchard, J.2    Scambler, P.3    Cowell, J.K.4
  • 16
    • 0026341035 scopus 로고
    • Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors
    • Kaneko Y, Homma C, Maseki N, Sakurai M, Hata J. 1991. Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors. Cancer Res 51:5937-5942.
    • (1991) Cancer Res , vol.51 , pp. 5937-5942
    • Kaneko, Y.1    Homma, C.2    Maseki, N.3    Sakurai, M.4    Hata, J.5
  • 18
    • 0015295131 scopus 로고
    • Mutation and cancer: A model for Wilms' tumor of the kidney
    • Knudson AG, Jr, Strong LC. 1972. Mutation and cancer: a model for Wilms' tumor of the kidney. J Natl Cancer Inst 48:313-324.
    • (1972) J Natl Cancer Inst , vol.48 , pp. 313-324
    • Knudson Jr., A.G.1    Strong, L.C.2
  • 19
    • 0242521297 scopus 로고    scopus 로고
    • Identification of a secreted BMP antagonist, ectodin, integrating BMP, FGF, and SHH signals from the tooth enamel knot
    • Laurikkala J, Kassai Y, Pakkasjä rvi L, Thesleff I, Itoh N. 2003. Identification of a secreted BMP antagonist, ectodin, integrating BMP, FGF, and SHH signals from the tooth enamel knot. Dev Biol 24:91-105.
    • (2003) Dev Biol , vol.24 , pp. 91-105
    • Laurikkala, J.1    Kassai, Y.2    Pakkasjärvi, L.3    Thesleff, I.4    Itoh, N.5
  • 24
    • 13944268747 scopus 로고    scopus 로고
    • The homeobox gene Gax inhibits angiogenesis through inhibition of nuclear factor-κB-dependent endothelial cell gene expression
    • DOI 10.1158/0008-5472.CAN-04-3431
    • Patel S, Leal AD, Gorski DH. 2005. The homeobox gene Gax inhibits angiogenesis through inhibition of nuclear factor-jB-dependent endothelial cell gene expression. Cancer Res 65:1414-1424. (Pubitemid 40270170)
    • (2005) Cancer Research , vol.65 , Issue.4 , pp. 1414-1424
    • Patel, S.1    Leal, A.D.2    Gorski, D.H.3
  • 26
    • 0032127486 scopus 로고    scopus 로고
    • Bax-mediated cell death by the Gax homeoprotein requires mitogen activation but is independent of cell cycle activity
    • DOI 10.1093/emboj/17.13.3576
    • Perlman H, Sata M, Le Roux A, Sedlak TW, Branellec D, Walsh K. 1998. Bax-mediated cell death by the Gax homeoprotein requires mitogen activation but is independent of cell cycle activity. EMBOJ 17:3576-3586. (Pubitemid 28327376)
    • (1998) EMBO Journal , vol.17 , Issue.13 , pp. 3576-3586
    • Perlman, H.1    Sata, M.2    Le Roux, A.3    Sedlak, T.W.4    Branellec, D.5    Walsh, K.6
  • 32
    • 25444455912 scopus 로고    scopus 로고
    • Wilms' tumour: Connecting tumorigenesis and organ development in the kidney
    • Rivera MN, Haber DA. 2005. Wilms' tumour: Connecting tumorigenesis and organ development in the kidney. Nat Rev Cancer 5:699-712.
    • (2005) Nat Rev Cancer , vol.5 , pp. 699-712
    • Rivera, M.N.1    Haber, D.A.2
  • 34
    • 43049157909 scopus 로고    scopus 로고
    • Wilms tumor genetics: Mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors
    • DOI 10.1002/gcc.20553
    • Ruteshouser EC, Robinson SM, Huff V. 2008. Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors. Genes Chromosomes Cancer 47:461-470. (Pubitemid 351657181)
    • (2008) Genes Chromosomes and Cancer , vol.47 , Issue.6 , pp. 461-470
    • Ruteshouser, E.C.1    Robinson, S.M.2    Huff, V.3
  • 37
    • 34547729171 scopus 로고    scopus 로고
    • Promoter hypermethylation of the RASSF1A gene predicts the poor outcome of patients with hepatoblastoma
    • DOI 10.1002/pbc.21031
    • Sugawara W, Haruta M, Sasaki F, Watanabe N, Tsunematsu Y, Kikuta A, Kaneko Y. 2007. Promoter hypermethylation of the RASSF1A gene predicts the poor outcome of patients with hepatoblastoma. Pediatr Blood Cancer 49:240-249. (Pubitemid 47236211)
    • (2007) Pediatric Blood and Cancer , vol.49 , Issue.3 , pp. 240-249
    • Sugawara, W.1    Haruta, M.2    Sasaki, F.3    Watanabe, N.4    Tsunematsu, Y.5    Kikuta, A.6    Kaneko, Y.7
  • 38
    • 0037422173 scopus 로고    scopus 로고
    • The parathyroid hormone-responsive B1 gene is interrupted by a t(1;7)(q42;p15) breakpoint associated with Wilms' tumour
    • DOI 10.1038/sj.onc.1206332
    • Vernon EG, Malik K, Reynolds P, Powlesland R, Dallosso AR, Jackson S, Henthorn K, Green ED, Brown KW. 2003. The parathyroid hormone-responsive B1 gene is interrupted by a t(1;7)(q42;p15) breakpoint associated with Wilms' tumour. Oncogene 22:1371-1380. (Pubitemid 36384599)
    • (2003) Oncogene , vol.22 , Issue.9 , pp. 1371-1380
    • Vernon, E.G.1    Malik, K.2    Reynolds, P.3    Powlesland, R.4    Dallosso, A.R.5    Jackson, S.6    Henthorn, K.7    Green, E.D.8    Brown, K.W.9
  • 42
    • 25444471062 scopus 로고    scopus 로고
    • Genomic profiling maps loss of heterozygosity and defines the timing and stage dependence of epigenetic and genetic events in Wilms' tumors
    • DOI 10.1158/1541-7786.MCR-05-0082
    • Yuan E, Li CM, Yamashiro DJ, Kandel J, Thaker H, Murty VV, Tycko B. 2005. Genomic profiling maps loss of heterozygosity and defines the timing and stage dependence of epigenetic and genetic events in Wilms' tumors. Mol Cancer Res 3:493-502. (Pubitemid 41377639)
    • (2005) Molecular Cancer Research , vol.3 , Issue.9 , pp. 493-502
    • Yuan, E.1    Li, C.-M.2    Yamashiro, D.J.3    Kandel, J.4    Thaker, H.5    Murty, V.V.6    Tycko, B.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.