메뉴 건너뛰기




Volumn 38, Issue 4, 2003, Pages 294-299

The Two-Hit Model for Wilms' Tumor: Where Are We 30 Years Later?

Author keywords

[No Author keywords available]

Indexed keywords

NEPHROBLASTOMA PROTEIN; PROTEIN; UNCLASSIFIED DRUG;

EID: 0345707482     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/gcc.10292     Document Type: Review
Times cited : (5)

References (46)
  • 3
    • 0027322848 scopus 로고
    • Excess of multifocal tumors in nephroblastoma: Implications for mechanisms of tumor development and genetic counseling
    • Bonaiti-Pellie C, Chompret A, Tournade MF, Lemerle J, Voute PA, Delemarre JF. 1993. Excess of multifocal tumors in nephroblastoma: Implications for mechanisms of tumor development and genetic counseling. Hum Genet 91:373-376.
    • (1993) Hum Genet , vol.91 , pp. 373-376
    • Bonaiti-Pellie, C.1    Chompret, A.2    Tournade, M.F.3    Lemerle, J.4    Voute, P.A.5    Delemarre, J.F.6
  • 4
    • 0029154687 scopus 로고
    • Second malignant neoplasms following treatment for Wilms' tumor: A report from the National Wilms' Tumor Study Group
    • Breslow NE, Takashima JR, Whitton JA, Moksness J, D'Angio GJ, Green DM. 1995. Second malignant neoplasms following treatment for Wilms' tumor: A report from the National Wilms' Tumor Study Group. J Clin Oncol 13:1851-1859.
    • (1995) J Clin Oncol , vol.13 , pp. 1851-1859
    • Breslow, N.E.1    Takashima, J.R.2    Whitton, J.A.3    Moksness, J.4    D'Angio, G.J.5    Green, D.M.6
  • 10
    • 0037313618 scopus 로고    scopus 로고
    • Coordinated regulation of life and death by RB
    • Chau BN, Wang JY. 2003. Coordinated regulation of life and death by RB. Nat Rev Cancer 3:130-138.
    • (2003) Nat Rev Cancer , vol.3 , pp. 130-138
    • Chau, B.N.1    Wang, J.Y.2
  • 11
    • 0036884829 scopus 로고    scopus 로고
    • The retinoblastoma tumour suppressor in development and cancer
    • Classon M, Harlow E. 2002. The retinoblastoma tumour suppressor in development and cancer. Nat Rev Cancer 2:910-917.
    • (2002) Nat Rev Cancer , vol.2 , pp. 910-917
    • Classon, M.1    Harlow, E.2
  • 13
    • 0024535228 scopus 로고
    • The human papilloma virus-16 E7 oncoprotein is able to bind to the retinoblastoma gene product
    • Dyson N, Howley PM, Munger K, Harlow E. 1989. The human papilloma virus-16 E7 oncoprotein is able to bind to the retinoblastoma gene product. Science 243:934-937.
    • (1989) Science , vol.243 , pp. 934-937
    • Dyson, N.1    Howley, P.M.2    Munger, K.3    Harlow, E.4
  • 14
    • 0021338486 scopus 로고
    • Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours
    • Fearon ER, Vogelstein B, Feinberg AP. 1984. Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours. Nature 309:176-178.
    • (1984) Nature , vol.309 , pp. 176-178
    • Fearon, E.R.1    Vogelstein, B.2    Feinberg, A.P.3
  • 16
    • 0037093084 scopus 로고    scopus 로고
    • Pregnancy outcome after treatment for Wilms tumor: A report from the National Wilms Tumor Study Group
    • Green DM, Peabody EM, Nan B, Peterson S, Kalapurakal JA, Breslow NE. 2002. Pregnancy outcome after treatment for Wilms tumor: A report from the National Wilms Tumor Study Group. J Clin Oncol 20:2506-2513.
    • (2002) J Clin Oncol , vol.20 , pp. 2506-2513
    • Green, D.M.1    Peabody, E.M.2    Nan, B.3    Peterson, S.4    Kalapurakal, J.A.5    Breslow, N.E.6
  • 17
    • 0023683531 scopus 로고
    • Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11
    • Grundy P, Koufos A, Morgan K, Li FP, Meadows AT, Cavenee WK. 1988. Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11. Nature 336:374-376.
    • (1988) Nature , vol.336 , pp. 374-376
    • Grundy, P.1    Koufos, A.2    Morgan, K.3    Li, F.P.4    Meadows, A.T.5    Cavenee, W.K.6
  • 21
    • 0028979148 scopus 로고
    • WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequences
    • Huff V, Jaffe N, Saunders GF, Strong LC, Villaba F, Ruteshouser EC. 1995. WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequences. Am J Hum Genet 56:84-90.
    • (1995) Am J Hum Genet , vol.56 , pp. 84-90
    • Huff, V.1    Jaffe, N.2    Saunders, G.F.3    Strong, L.C.4    Villaba, F.5    Ruteshouser, E.C.6
  • 23
    • 0015043748 scopus 로고
    • Mutation and cancer: Statistical study of retinoblastoma
    • Knudson AG. 1971. Mutation and cancer: Statistical study of retinoblastoma. Proc Natl Acad Sci USA 68:820-823.
    • (1971) Proc Natl Acad Sci USA , vol.68 , pp. 820-823
    • Knudson, A.G.1
  • 24
    • 0015295131 scopus 로고
    • Mutation and cancer: A model for Wilms' tumor of the kidney
    • Knudson AG Jr., Strong LC. 1972a. 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
  • 25
    • 0015402175 scopus 로고
    • Mutation and cancer: Neuroblastoma and pheochromocytoma
    • Knudson AG Jr., Strong LC. 1972b. Mutation and cancer: Neuroblastoma and pheochromocytoma. Am J Hum Genet 24:514-532.
    • (1972) Am J Hum Genet , vol.24 , pp. 514-532
    • Knudson Jr., A.G.1    Strong, L.C.2
  • 30
    • 0032053822 scopus 로고    scopus 로고
    • Linkage of familial Wilms' tumor predisposition to chromosome 19 and two-locus model for the etiology of familial tumors
    • McDonald JM, Douglass EC, Fisher R, Geiser CF, Krill CE, Strong LC, Virshup D, Huff V. 1998. Linkage of familial Wilms' tumor predisposition to chromosome 19 and two-locus model for the etiology of familial tumors. Cancer Res 58:1387-1390.
    • (1998) Cancer Res , vol.58 , pp. 1387-1390
    • McDonald, J.M.1    Douglass, E.C.2    Fisher, R.3    Geiser, C.F.4    Krill, C.E.5    Strong, L.C.6    Virshup, D.7    Huff, V.8
  • 32
    • 0024428508 scopus 로고
    • The E6 and E7 genes of the human papillomavirus type 16 together are necessary and sufficient for transformation of primary human keratinocytes
    • Munger K, Phelps WC, Bubb V, Howley PM, Schlegel R. 1989. The E6 and E7 genes of the human papillomavirus type 16 together are necessary and sufficient for transformation of primary human keratinocytes. J Virol 63:4417-4421.
    • (1989) J Virol , vol.63 , pp. 4417-4421
    • Munger, K.1    Phelps, W.C.2    Bubb, V.3    Howley, P.M.4    Schlegel, R.5
  • 33
    • 0028918615 scopus 로고
    • Non-11p constitutional chromosome abnormalities in Wilms' tumor patients
    • Olson JM, Hamilton A, Breslow NE. 1995. Non-11p constitutional chromosome abnormalities in Wilms' tumor patients. Med Pediatr Oncol 24:305-309.
    • (1995) Med Pediatr Oncol , vol.24 , pp. 305-309
    • Olson, J.M.1    Hamilton, A.2    Breslow, N.E.3
  • 34
    • 0032971182 scopus 로고    scopus 로고
    • WT1 and GATA1 expression in myelodysplastic syndrome and acute leukemia
    • Patmasiriwat P, Fraizer G, Kantarjian H, Saunders GF. 1999. WT1 and GATA1 expression in myelodysplastic syndrome and acute leukemia. Leukemia 13:891-900.
    • (1999) Leukemia , vol.13 , pp. 891-900
    • Patmasiriwat, P.1    Fraizer, G.2    Kantarjian, H.3    Saunders, G.F.4
  • 36
    • 0017883401 scopus 로고
    • Chromosomal imbalance in the aniridia-Wilms' tumor association: 11p interstitial deletion
    • Riccardi VM, Sujansky E, Smith, AC, Francke U. 1978. Chromosomal imbalance in the aniridia-Wilms' tumor association: 11p interstitial deletion. Pediatrics 61:604-610.
    • (1978) Pediatrics , vol.61 , pp. 604-610
    • Riccardi, V.M.1    Sujansky, E.2    Smith, A.C.3    Francke, U.4
  • 38
    • 18344412519 scopus 로고    scopus 로고
    • Risk of cancer among offspring of childhood-cancer survivors
    • Association of the Nordic Cancer Registries and the Nordic Society of Paediatric Haematology and Oncology
    • Sankila R, Olsen JH, Anderson H, Garwicz S, Glattre E, Hertz H, Langmark F, Lanning M, Moller T, Tulinius H. 1998. Risk of cancer among offspring of childhood-cancer survivors. Association of the Nordic Cancer Registries and the Nordic Society of Paediatric Haematology and Oncology. N Engl J Med 338:1339-1344.
    • (1998) N Engl J Med , vol.338 , pp. 1339-1344
    • Sankila, R.1    Olsen, J.H.2    Anderson, H.3    Garwicz, S.4    Glattre, E.5    Hertz, H.6    Langmark, F.7    Lanning, M.8    Moller, T.9    Tulinius, H.10
  • 40
    • 0031410720 scopus 로고    scopus 로고
    • A splicing mutation in RB1 in low penetrance retinoblastoma
    • Schubert EL, Strong LC, Hansen MF. 1997. A splicing mutation in RB1 in low penetrance retinoblastoma. Hum Genet 100:557-563.
    • (1997) Hum Genet , vol.100 , pp. 557-563
    • Schubert, E.L.1    Strong, L.C.2    Hansen, M.F.3
  • 41
    • 0033516621 scopus 로고    scopus 로고
    • Mulibrey nanism and Wilms tumor
    • Seemanova E, Bartsch O. 1999. Mulibrey nanism and Wilms tumor. Am J Hum Genet 85:76-78.
    • (1999) Am J Hum Genet , vol.85 , pp. 76-78
    • Seemanova, E.1    Bartsch, O.2
  • 42
    • 0023914010 scopus 로고
    • Association between an oncogene and an anti-oncogene: The adenovirus E1A proteins bind to the retinoblastoma gene product
    • Whyte P, Buchkovich KJ, Horowitz JM, Friend SH, Raybuck M, Weinberg RA, Harlow E. 1988. Association between an oncogene and an anti-oncogene: The adenovirus E1A proteins bind to the retinoblastoma gene product. Nature 334:124-129.
    • (1988) Nature , vol.334 , pp. 124-129
    • Whyte, P.1    Buchkovich, K.J.2    Horowitz, J.M.3    Friend, S.H.4    Raybuck, M.5    Weinberg, R.A.6    Harlow, E.7
  • 43
    • 34250134720 scopus 로고
    • Tumours and hemihypertrophy associated with Wiedemann-Beckwith syndrome
    • Wiedemann HR. 1983. Tumours and hemihypertrophy associated with Wiedemann-Beckwith syndrome. Eur J Pediatr 141:129.
    • (1983) Eur J Pediatr , vol.141 , pp. 129
    • Wiedemann, H.R.1
  • 44
    • 0023831210 scopus 로고
    • Genomic imprinting and carcinogenesis
    • Wilkins RJ. 1988. Genomic imprinting and carcinogenesis. Lancet 1:329-331.
    • (1988) Lancet , vol.1 , pp. 329-331
    • Wilkins, R.J.1
  • 46
    • 0027496294 scopus 로고
    • Imprinting of human H19: Allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching
    • Zhang Y, Shields T, Crenshak T, Hao Y, Moulton T, Tycko B. 1993. Imprinting of human H19: Allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching. Am J Hum Genet 53:113-124.
    • (1993) Am J Hum Genet , vol.53 , pp. 113-124
    • Zhang, Y.1    Shields, T.2    Crenshak, T.3    Hao, Y.4    Moulton, T.5    Tycko, B.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.