메뉴 건너뛰기




Volumn 16, Issue 7, 2010, Pages 2036-2045

Subtype-specific FBXW7 mutation and MYCN copy number gain in Wilms' tumor

Author keywords

[No Author keywords available]

Indexed keywords

UBIQUITIN PROTEIN LIGASE E3;

EID: 77950641105     PISSN: 10780432     EISSN: None     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-09-2890     Document Type: Article
Times cited : (62)

References (48)
  • 1
    • 33749031535 scopus 로고    scopus 로고
    • The many facets of the Wilms' tumour gene, WT1
    • Hohenstein P, Hastie ND. The many facets of the Wilms' tumour gene, WT1. Hum Mol Genet 2006;15 Spec No 2:R196-201.
    • (2006) Hum Mol Genet , vol.15 , Issue.SPEC NO 2
    • Hohenstein, P.1    Hastie, N.D.2
  • 2
    • 0033566764 scopus 로고    scopus 로고
    • Mutational activation of the β-catenin proto-oncogene is a common event in the development of Wilms' tumors
    • Koesters R, Ridder R, Kopp-Schneider A, et al. Mutational activation of the β-catenin proto-oncogene is a common event in the development of Wilms' tumors. Cancer Res 1999;59:3880-3882
    • (1999) Cancer Res , vol.59 , pp. 3880-3882
    • Koesters, R.1    Ridder, R.2    Kopp-Schneider, A.3
  • 3
    • 9644265525 scopus 로고    scopus 로고
    • CTNNB1 mutations and overexpression of Wnt/β-catenin target genes in WT1-mutant Wilms' tumors
    • Li CM, Kim CE, Margolin AA, et al. CTNNB1 mutations and overexpression of Wnt/β-catenin target genes in WT1-mutant Wilms' tumors. Am J Pathol 2004;165:1943-1953
    • (2004) Am J Pathol , vol.165 , pp. 1943-1953
    • Li, C.M.1    Kim, C.E.2    Margolin, A.A.3
  • 4
    • 0033677022 scopus 로고    scopus 로고
    • Frequent association of β-catenin and WT1 mutations in Wilms tumors
    • Maiti S, Alam R, Amos CI, Huff V. Frequent association of β-catenin and WT1 mutations in Wilms tumors. Cancer Res 2000;60:6288-6292
    • (2000) Cancer Res , vol.60 , pp. 6288-6292
    • Maiti, S.1    Alam, R.2    Amos, C.I.3    Huff, V.4
  • 5
    • 52049100974 scopus 로고    scopus 로고
    • Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin-associated protein β1 gene CTNNB1 for patients with Wilms tumors: Results of long-term surveillance of 71 patients from International Society of Pediatric Oncology Study 9/Society for Pediatric Oncology
    • Royer-Pokora B, Weirich A, Schumacher V, et al. Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin-associated protein β1 gene CTNNB1 for patients with Wilms tumors: results of long-term surveillance of 71 patients from International Society of Pediatric Oncology Study 9/Society for Pediatric Oncology. Cancer 2008;113:1080-1089
    • (2008) Cancer , vol.113 , pp. 1080-1089
    • Royer-Pokora, B.1    Weirich, A.2    Schumacher, V.3
  • 7
    • 33846846526 scopus 로고    scopus 로고
    • An X chromosome gene, WTX, is commonly inactivated in Wilms tumor
    • Rivera MN, Kim WJ, Wells J, et al. An X chromosome gene, WTX, is commonly inactivated in Wilms tumor. Science 2007;315:642-645
    • (2007) Science , vol.315 , pp. 642-645
    • Rivera, M.N.1    Kim, W.J.2    Wells, J.3
  • 8
    • 43049157909 scopus 로고    scopus 로고
    • Wilms tumor genetics: Mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors
    • Ruteshouser EC, Robinson SM, Huff V. Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors. Genes Chromosomes Cancer 2008;47:461-470
    • (2008) Genes Chromosomes Cancer , vol.47 , pp. 461-470
    • Ruteshouser, E.C.1    Robinson, S.M.2    Huff, V.3
  • 9
    • 0027285258 scopus 로고
    • Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
    • Ogawa O, Eccles MR, Szeto J, et al. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour. Nature 1993; 362:749-751
    • (1993) Nature , vol.362 , pp. 749-751
    • Ogawa, O.1    Eccles, M.R.2    Szeto, J.3
  • 11
    • 33749266701 scopus 로고    scopus 로고
    • Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour
    • Scott RH, Stiller CA, Walker L, Rahman N. Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour. J Med Genet 2006;43:705-715
    • (2006) J Med Genet , vol.43 , pp. 705-715
    • Scott, R.H.1    Stiller, C.A.2    Walker, L.3    Rahman, N.4
  • 12
    • 0028168146 scopus 로고
    • Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbours p53 gene mutations
    • Bardeesy N, Falkoff D, Petruzzi MJ, et al. Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbours p53 gene mutations. Nat Genet 1994;7:91-97
    • (1994) Nat Genet , vol.7 , pp. 91-97
    • Bardeesy, N.1    Falkoff, D.2    Petruzzi, M.J.3
  • 13
    • 0036157514 scopus 로고    scopus 로고
    • Revised International Society of Paediatric Oncology (SIOP) working classification of renal tumors of childhood
    • Vujanic GM, Sandstedt B, Harms D, Kelsey A, Leuschner I, de Kraker J. Revised International Society of Paediatric Oncology (SIOP) working classification of renal tumors of childhood. Med Pediatr Oncol 2002;38:79-82.
    • (2002) Med Pediatr Oncol , vol.38 , pp. 79-82
    • Vujanic, G.M.1    Sandstedt, B.2    Harms, D.3    Kelsey, A.4    Leuschner, I.5    De Kraker, J.6
  • 14
    • 35148842479 scopus 로고    scopus 로고
    • FBXW7/hCDC4 is a general tumor suppressor in human cancer
    • Akhoondi S, Sun D, von der Lehr N, et al. FBXW7/hCDC4 is a general tumor suppressor in human cancer. Cancer Res 2007;67:9006-9012
    • (2007) Cancer Res , vol.67 , pp. 9006-9012
    • Akhoondi, S.1    Sun, D.2    Von Der Lehr, N.3
  • 15
    • 0021063273 scopus 로고
    • Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumour
    • Schwab M, Alitalo K, Klempnauer KH, et al. Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumour. Nature 1983;305: 245-248
    • (1983) Nature , vol.305 , pp. 245-248
    • Schwab, M.1    Alitalo, K.2    Klempnauer, K.H.3
  • 17
    • 12744262848 scopus 로고    scopus 로고
    • The biologic basis for neuroblastoma heterogeneity and risk stratification
    • Maris JM. The biologic basis for neuroblastoma heterogeneity and risk stratification. Curr Opin Pediatr 2005;17:7-13.
    • (2005) Curr Opin Pediatr , vol.17 , pp. 7-13
    • Maris, J.M.1
  • 19
    • 33646911907 scopus 로고    scopus 로고
    • Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arrays
    • Beroukhim R, Lin M, Park Y, et al. Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arrays. PLoS Comput Biol 2006;2:e41.
    • (2006) PLoS Comput Biol , vol.2
    • Beroukhim, R.1    Lin, M.2    Park, Y.3
  • 20
    • 68549123567 scopus 로고    scopus 로고
    • WNT/β-catenin pathway activation in Wilms tumors: A unifying mechanism with multiple entries?
    • Corbin M, de Reynies A, Rickman DS, et al. WNT/β-catenin pathway activation in Wilms tumors: a unifying mechanism with multiple entries? Genes Chromosomes Cancer 2009;48:816-827
    • (2009) Genes Chromosomes Cancer , vol.48 , pp. 816-827
    • Corbin, M.1    De Reynies, A.2    Rickman, D.S.3
  • 21
    • 2642552403 scopus 로고    scopus 로고
    • Myogenesis in Wilms' tumors is associated with mutations of the WT1 gene and activation of Bcl-2 and the Wnt signaling pathway
    • Fukuzawa R, Heathcott RW, Sano M, Morison IM, Yun K, Reeve AE. Myogenesis in Wilms' tumors is associated with mutations of the WT1 gene and activation of Bcl-2 and the Wnt signaling pathway. Pediatr Dev Pathol 2004;7:125-137
    • (2004) Pediatr Dev Pathol , vol.7 , pp. 125-137
    • Fukuzawa, R.1    Heathcott, R.W.2    Sano, M.3    Morison, I.M.4    Yun, K.5    Reeve, A.E.6
  • 22
    • 0030889197 scopus 로고    scopus 로고
    • Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology
    • Schumacher V, Schneider S, Figge A, et al. Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology. Proc Natl Acad Sci U S A 1997;94:3972-3977
    • (1997) Proc Natl Acad Sci U S A , vol.94 , pp. 3972-3977
    • Schumacher, V.1    Schneider, S.2    Figge, A.3
  • 23
    • 0037501301 scopus 로고    scopus 로고
    • Two molecular subgroups of Wilms' tumors with or without WT1 mutations
    • Schumacher V, Schuhen S, Sonner S, et al. Two molecular subgroups of Wilms' tumors with or without WT1 mutations. Clin Cancer Res 2003;9:2005-2014
    • (2003) Clin Cancer Res , vol.9 , pp. 2005-2014
    • Schumacher, V.1    Schuhen, S.2    Sonner, S.3
  • 24
    • 42049087606 scopus 로고    scopus 로고
    • Correlation between β-catenin mutations and expression of Wnt-signaling target genes in hepatocellular carcinoma
    • Austinat M, Dunsch R, Wittekind C, Tannapfel A, Gebhardt R, Gaunitz F. Correlation between β-catenin mutations and expression of Wnt-signaling target genes in hepatocellular carcinoma. Mol Cancer 2008;7:21.
    • (2008) Mol Cancer , vol.7 , pp. 21
    • Austinat, M.1    Dunsch, R.2    Wittekind, C.3    Tannapfel, A.4    Gebhardt, R.5    Gaunitz, F.6
  • 25
    • 45349090812 scopus 로고    scopus 로고
    • Duplication of paternal IGF2 or loss of maternal IGF2 imprinting occurs in half of Wilms tumors with various structural WT1 abnormalities
    • Haruta M, Arai Y, Sugawara W, et al. Duplication of paternal IGF2 or loss of maternal IGF2 imprinting occurs in half of Wilms tumors with various structural WT1 abnormalities. Genes Chromosomes Cancer 2008;47:712-727
    • (2008) Genes Chromosomes Cancer , vol.47 , pp. 712-727
    • Haruta, M.1    Arai, Y.2    Sugawara, W.3
  • 26
    • 10644269326 scopus 로고    scopus 로고
    • Fbxw7/Cdc4 is a p53-dependent, haploinsufficient tumour suppressor gene
    • Mao JH, Perez-Losada J, Wu D, et al. Fbxw7/Cdc4 is a p53-dependent, haploinsufficient tumour suppressor gene. Nature 2004;432: 775-779
    • (2004) Nature , vol.432 , pp. 775-779
    • Mao, J.H.1    Perez-Losada, J.2    Wu, D.3
  • 27
    • 38549086019 scopus 로고    scopus 로고
    • FBW7 ubiquitin ligase: A tumour suppressor at the crossroads of cell division, growth and differentiation
    • Welcker M, Clurman BE. FBW7 ubiquitin ligase: a tumour suppressor at the crossroads of cell division, growth and differentiation. Nat Rev Cancer 2008;8:83-93.
    • (2008) Nat Rev Cancer , vol.8 , pp. 83-93
    • Welcker, M.1    Clurman, B.E.2
  • 28
    • 43049139905 scopus 로고    scopus 로고
    • BCR-ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros
    • Mullighan CG, Miller CB, Radtke I, et al. BCR-ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros. Nature 2008; 453:110-114
    • (2008) Nature , vol.453 , pp. 110-114
    • Mullighan, C.G.1    Miller, C.B.2    Radtke, I.3
  • 29
    • 70349232830 scopus 로고    scopus 로고
    • WT1 mutations in T-ALL
    • Tosello V, Mansour MR, Barnes K, et al. WT1 mutations in T-ALL. Blood 2009;114:1038-1045
    • (2009) Blood , vol.114 , pp. 1038-1045
    • Tosello, V.1    Mansour, M.R.2    Barnes, K.3
  • 30
    • 54049118823 scopus 로고    scopus 로고
    • Oncogenic mutations of ALK kinase in neuroblastoma
    • Chen Y, Takita J, Choi YL, et al. Oncogenic mutations of ALK kinase in neuroblastoma. Nature 2008;455:971-974
    • (2008) Nature , vol.455 , pp. 971-974
    • Chen, Y.1    Takita, J.2    Choi, Y.L.3
  • 31
    • 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
    • Yuan E, Li CM, Yamashiro DJ, et al. Genomic profiling maps loss of heterozygosity and defines the timing and stage dependence of epigenetic and genetic events in Wilms' tumors. Mol Cancer Res 2005; 3:493-502.
    • (2005) Mol Cancer Res , vol.3 , pp. 493-502
    • Yuan, E.1    Li, C.M.2    Yamashiro, D.J.3
  • 32
    • 0025033343 scopus 로고
    • N-myc oncogene amplification in paediatric tumours
    • McQuaid S, O'Meara A. N-myc oncogene amplification in paediatric tumours. Ir J Med Sci 1990;159:172-174
    • (1990) Ir J Med Sci , vol.159 , pp. 172-174
    • McQuaid, S.1    O'Meara, A.2
  • 35
    • 20044391414 scopus 로고    scopus 로고
    • Relationship between MYCN copy number and expression in rhabdomyosarcomas and correlation with adverse prognosis in the alveolar subtype
    • Williamson D, Lu YJ, Gordon T, et al. Relationship between MYCN copy number and expression in rhabdomyosarcomas and correlation with adverse prognosis in the alveolar subtype. J Clin Oncol 2005;23: 880-888
    • (2005) J Clin Oncol , vol.23 , pp. 880-888
    • Williamson, D.1    Lu, Y.J.2    Gordon, T.3
  • 36
    • 0036245047 scopus 로고    scopus 로고
    • MYCC and MYCN oncogene amplification in medulloblastoma. A fluorescence in situ hybridization study on paraffin sections from the Children's Oncology Group
    • Aldosari N, Bigner SH, Burger PC, et al. MYCC and MYCN oncogene amplification in medulloblastoma. A fluorescence in situ hybridization study on paraffin sections from the Children's Oncology Group. Arch Pathol Lab Med 2002;126:540-544
    • (2002) Arch Pathol Lab Med , vol.126 , pp. 540-544
    • Aldosari, N.1    Bigner, S.H.2    Burger, P.C.3
  • 37
    • 63749118521 scopus 로고    scopus 로고
    • Outcome prediction in pediatric medulloblastoma based on DNA copy-number aberrations of chromosomes 6q and 17q and the MYC and MYCN loci
    • Pfister S, Remke M, Benner A, et al. Outcome prediction in pediatric medulloblastoma based on DNA copy-number aberrations of chromosomes 6q and 17q and the MYC and MYCN loci. J Clin Oncol 2009;27:1627-1636
    • (2009) J Clin Oncol , vol.27 , pp. 1627-1636
    • Pfister, S.1    Remke, M.2    Benner, A.3
  • 38
    • 0021241701 scopus 로고
    • Expression and amplification of the N-myc gene in primary retinoblastoma
    • Lee WH, Murphree AL, Benedict WF. Expression and amplification of the N-myc gene in primary retinoblastoma. Nature 1984;309:458-460
    • (1984) Nature , vol.309 , pp. 458-460
    • Lee, W.H.1    Murphree, A.L.2    Benedict, W.F.3
  • 39
    • 34249004558 scopus 로고    scopus 로고
    • One hit, two hits, three hits, more? Genomic changes in the development of retinoblastoma
    • Corson TW, Gallie BL. One hit, two hits, three hits, more? Genomic changes in the development of retinoblastoma. Genes Chromosomes Cancer 2007;46:617-634
    • (2007) Genes Chromosomes Cancer , vol.46 , pp. 617-634
    • Corson, T.W.1    Gallie, B.L.2
  • 40
    • 0023877551 scopus 로고
    • N-myc oncogene expression in histopathologically unrelated bilateral pediatric renal tumors
    • Nisen PD, Rich MA, Gloster E, et al. N-myc oncogene expression in histopathologically unrelated bilateral pediatric renal tumors. Cancer 1988;61:1821-1826
    • (1988) Cancer , vol.61 , pp. 1821-1826
    • Nisen, P.D.1    Rich, M.A.2    Gloster, E.3
  • 42
    • 3342939836 scopus 로고    scopus 로고
    • Prognostic classification of relapsing favorable histology Wilms tumor using cDNA microarray expression profiling and support vector machines
    • Williams RD, Hing SN, Greer BT, et al. Prognostic classification of relapsing favorable histology Wilms tumor using cDNA microarray expression profiling and support vector machines. Genes Chromosomes Cancer 2004;41:65-79.
    • (2004) Genes Chromosomes Cancer , vol.41 , pp. 65-79
    • Williams, R.D.1    Hing, S.N.2    Greer, B.T.3
  • 43
    • 41349121558 scopus 로고    scopus 로고
    • New prognostic markers revealed by evaluation of genes correlated with clinical parameters in Wilms tumors
    • Wittmann S, Wunder C, Zirn B, et al. New prognostic markers revealed by evaluation of genes correlated with clinical parameters in Wilms tumors. Genes Chromosomes Cancer 2008;47:386-395
    • (2008) Genes Chromosomes Cancer , vol.47 , pp. 386-395
    • Wittmann, S.1    Wunder, C.2    Zirn, B.3
  • 44
    • 33645236966 scopus 로고    scopus 로고
    • Expression profiling of Wilms tumors reveals new candidate genes for different clinical parameters
    • Zirn B, Hartmann O, Samans B, et al. Expression profiling of Wilms tumors reveals new candidate genes for different clinical parameters. Int J Cancer 2006;118:1954-1962
    • (2006) Int J Cancer , vol.118 , pp. 1954-1962
    • Zirn, B.1    Hartmann, O.2    Samans, B.3
  • 45
    • 48349147602 scopus 로고    scopus 로고
    • High cyclin e staining index in blastemal, stromal or epithelial cells is correlated with tumor aggressiveness in patients with nephroblastoma
    • Berrebi D, Leclerc J, Schleiermacher G, et al. High cyclin E staining index in blastemal, stromal or epithelial cells is correlated with tumor aggressiveness in patients with nephroblastoma. PLoS ONE 2008;3: e2216.
    • (2008) PLoS ONE , vol.3
    • Berrebi, D.1    Leclerc, J.2    Schleiermacher, G.3
  • 46
    • 57849107571 scopus 로고    scopus 로고
    • Stabilization of N-Myc is a critical function of Aurora a in human neuroblastoma
    • Otto T, Horn S, Brockmann M, et al. Stabilization of N-Myc is a critical function of Aurora A in human neuroblastoma. Cancer Cell 2009; 15:67-78.
    • (2009) Cancer Cell , vol.15 , pp. 67-78
    • Otto, T.1    Horn, S.2    Brockmann, M.3
  • 47
    • 33745146147 scopus 로고    scopus 로고
    • Molecularly guided therapy of neuroblastoma: A review of different approaches
    • Tonini GP, Pistoia V. Molecularly guided therapy of neuroblastoma: a review of different approaches. Curr Pharm Des 2006;12:2303-2317
    • (2006) Curr Pharm des , vol.12 , pp. 2303-2317
    • Tonini, G.P.1    Pistoia, V.2
  • 48


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.