Genetic mosaicism in normal tissues of Wilms' tumour patients (original) (raw)

• Breslow, N., Beckwith, J.B., Ciol, M. & Sharples, K. Age distribution of Wilms' tumor: report from the National Wilms' Tumor Study. Cancer Res. 48, 1653–1657 (1988).
  CAS PubMed Google Scholar
• Matsunaga, E. Genetics of Wilms' tumor. Hum. Genet. 57, 231–246 (1981).
  Article CAS PubMed Google Scholar
• Koufos, A. et al. Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour. Nature 309, 170–172 (1984).
  Article CAS PubMed Google Scholar
• Orkin, S.H., Goldman, D.S. & Sallan, S.E. Development of homozygosity for chromosome 11p markers in Wilms' tumor. Nature 309, 172–174 (1984).
  Article CAS PubMed Google Scholar
• Fearon, E.R., Vogelstein, B. & Feinberg, A.P. Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours. Nature 309, 176–178 (1984).
  Article CAS PubMed Google Scholar
• Dao, D.D. et al. Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms' tumor. Am. J. hum. Genet. 41, 202–217 (1987).
  CAS PubMed PubMed Central Google Scholar
• Wadey, R.B. et al. Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11. Oncogene 5, 901–907 (1990).
  CAS PubMed Google Scholar
• Schroeder, W.T. et al. Nonrandom loss of maternal chromosome 11 alleles in Wilms' tumors. Am. J. hum. Genet. 40, 413–420 (1987).
  CAS PubMed PubMed Central Google Scholar
• Call, K.M. et al. Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell 60, 509–520 (1990).
  Article CAS PubMed Google Scholar
• Gessler, M. et al. Homozygous deletion in Wilms' tumours of a zinc-finger gene identified by chromosome jumping. Nature 343, 774–778 (1990).
  Article CAS PubMed Google Scholar
• Huff, V. et al. Evidence for WT1 as a Wilms' tumor (WT) Gene: Intragenic germinal deletion in bilateral WT. Am. J. hum. Genet. 48, 997–1003 (1991).
  CAS PubMed PubMed Central Google Scholar
• Haber, D.A. et al. An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor. Cell 61, 1257–1269 (1990).
  Article CAS PubMed Google Scholar
• Pelletier, J. et al. WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour. Nature 353, 431–434 (1991).
  Article CAS PubMed Google Scholar
• Huff, V., Villalba, F., Strong, L.C. & Saunders, G.F. Alteration of the WT1 gene in patients with Wilms' tumor and genitourinary anomalies. Am. J. hum. Genet. 49S, 44 (1991).
  Google Scholar
• Pelletier, J. et al. Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Cell 67, 437–447 (1991).
  Article CAS PubMed Google Scholar
• Little, M.H. et al. Zinc finger point mutations within the WT1 gene in Wilms' tumor patients. Proc. natn. Acad. Sci. U.S.A. 89, 4791–4795 (1992).
  Article CAS Google Scholar
• Reeve, A.E., Shih, S.A., Raizis, A.M. & Feinberg, A.P. Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells. Molec. cell. Biol. 9, 1799–1803 (1989).
  Article CAS PubMed PubMed Central Google Scholar
• Mannens, M. et al. Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours. Hum. Genet. 81, 41–48 (1988).
  Article CAS PubMed Google Scholar
• Henry, I. et al. Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms' tumor and in familial adrenocortical carcinoma. Proc. natn. Acad. Sci. U.S.A. 86, 3247–3251 (1989).
  Article CAS Google Scholar
• Wiedemann, H.R. Complexe malformatif familial avec hernie ombilicale et macroglossie—un “syndrome nouveau”? J. Genet. Hum. 13, 223–232 (1964).
  CAS PubMed Google Scholar
• Beckwith, J.B. Macroglossia, omphalocele, adrenal cytomegaly, gigantism, and hyperplastic visceromegaly. Birth Defects 5, 188–196 (1969).
  Google Scholar
• Sotela-Avila, C., Gonzalez-Crussi, F. & Fowler, J.W. Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential. J. Pediatr. 96, 47–50 (1980).
  Article Google Scholar
• Ping, A.J. et al. Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am. J. hum. Genet. 44, 720–723 (1989).
  CAS PubMed PubMed Central Google Scholar
• Koufos, A. et al. Familial Wiedemann-Beckwith syndrome and a second Wilms' tumor locus both map to 11p15.5. Am. J. hum Genet. 44, 711–719 (1989).
  CAS PubMed PubMed Central Google Scholar
• Grundy, P. et al. Chromosome 11 uniparental isodisomy predisposing to embryonal neoplasms. Lancet 338, 1079–1080 (1991).
  Article CAS PubMed Google Scholar
• Henry, I. et al. Uniparental paternal disomy in a genetic cancer-predisposing syndrome. Nature 351, 665–670 (1991).
  Article CAS PubMed Google Scholar
• Henry, I. et al. Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-ferterlization event. Eur. J. hum. Genet. 1, 19–29 (1992).
  Article Google Scholar
• Compton, D.A. et al. Definition of the limits of the Wilms' tumor locus on human chromosome 11p13. Genomics 6, 309–315 (1990).
  Article CAS PubMed Google Scholar
• Schneid, H., Vazquez, M.P., Seurin, D. & le Bouc, Y. Loss of heterozygosity in non-tumoral tissue in two children with Beckwith-Wiedemann syndrome. Growth Regul. 1, 168–170 (1991).
  CAS PubMed Google Scholar
• Clayton-Smith, J., Read, A.P. & Donnai, D. Monozygotic twinning and Wiedemann-Beckwith syndrome. Am J. med. Genet. 42, 633–637 (1992).
  Article CAS PubMed Google Scholar
• Fraumeni, J.F. & Geiser, C.F., Manning, M.D. Wilms' tumor and congenital hemihypertrophy: report of five new cases and review of the literature. Pediatrics 40, 886–899 (1967).
  PubMed Google Scholar
• Scrable, H. et al. A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting. Proc. natn. Acad. Sci. U.S.A. 86, 7480–7484 (1989).
  Article CAS Google Scholar
• Williams, J.C., Brown, K.W., Mott, M.G. & Maitland, N.J. Maternal allele loss in Wilms' tumour. Lancet 1, 283–284 (1989).
  Article CAS PubMed Google Scholar
• Dowdy, S.F. et al. Suppression of tumorigenicity in Wilms' tumor by the 11p15.5-p14 region of chromosome 11. Science 254, 293–295 (1991).
  Article CAS PubMed Google Scholar
• Scott, J. et al. Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues. Nature 317, 260–262 (1985).
  Article CAS PubMed Google Scholar
• Poirier, F. et al. The murine H19 gene is activated during embryonic stem cell differentiation in vitro and at the time of implantation in the developing embryo. Development 113, 1105–1114 (1991).
  CAS PubMed Google Scholar
• DeChiara, T.M., Robertson, E.J. & Efstratiadis, A. Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64, 849–859 (1991).
  Article CAS PubMed Google Scholar
• Ferguson-Smith, A.C., Cattanach, B.M., Barton, S.C., Beechey, C.V. & Surani, A.M. Embryological and molecular investigations of parental imprinting on mouse chromosome 7. Nature 351, 667–670 (1991).
  Article CAS PubMed Google Scholar
• Bartolomei, M.S., Zemel, S. & Tilghman, S.M. Parental imprinting of the mouse H19 gene. Nature 351, 153–155 (1991).
  Article CAS PubMed Google Scholar
• Zhang, Y. & Tycko, B. Monoallelic expression of the human H19 gene. Nature Genet. 1, 40–44 (1992).
  Article CAS PubMed Google Scholar
• Brunkow, M.E. & Tilghman, S.M. Ectopic expression of the H19 gene in mice causes prenatal lethality. Genes Dev. 5, 1092–1101 (1991).
  Article CAS PubMed Google Scholar
• Jeanpierre, C. et al. Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms' tumor. Genomics 7, 434–438 (1990).
  Article CAS PubMed Google Scholar
• Knudson, A.G. & Strong, L.C. Mutation and Cancer: A model for Wilms' tumor of the kidney. J. natn. Cancer Inst. 48, 313–324 (1972).
  Google Scholar
• Miller, S.A., Dykes, D.D. & Polesky, H.F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucl. Acids Res. 16, 1215 (1988).
  Article CAS PubMed PubMed Central Google Scholar
• Huff, V., Compton, D.A., Strong, L.C. & Saunders, G.F. A panel of restriction fragment length polymorphisms for chromosomal band 11 p13. Hum Genet. 84, 253–257 (1990).
  Article CAS PubMed Google Scholar
• Capon, D.J., Chen, E.Y., Levinson, A.D., Seeburg, P.H. & Goeddel, D.V. Complete nucleotide sequences of the T24 human bladder carcinoma oncogene and its normal homologue. Nature 302, 33–37 (1983).
  Article CAS PubMed Google Scholar
• Bell, G.I., Horita, S. & Karam, J.H. A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus. Diabetes 33, 176–183 (1984).
  Article CAS PubMed Google Scholar
• Barker, D., Holm, T. & White, R. A locus on chromosome 11 p with multiple restriction site polymorphisms. Am. J. hum. Genet. 36, 1159–1171 (1984).
  CAS PubMed PubMed Central Google Scholar
• Hendy, G.N., Kronenberg, H.M., Potts, J.T., Jr. & Rich, A. Nucleotide sequence of cloned cDNAs encoding human preproparathyroid hormone. Proc. natn. Acad. Sci. U.S.A. 78, 7365–7369 (1981).
  Article CAS Google Scholar
• Nakamura, Y. et al. Isolation and mapping of a polymorphic DNA sequence (pHBI59) on chromosome 11 [_D11S146_]. Nucl. Acids Res. 16, 10404 (1988).
  Article CAS PubMed PubMed Central Google Scholar
• Maslen, G.L. et al. Seven polymorphic loci mapping to human chromosomal region 11q22-qter. Genomics 2, 66–75 (1988).
  Article CAS PubMed Google Scholar
• Kessling, A.M., Horsthemke, B. & Humphries, S.E. A study of DNA polymorphisms around the human apolipoprotein A1 gene in hyperlipidaemic and normal individuals. Clin. Genet. 28, 296–306 (1985).
  Article CAS PubMed Google Scholar