A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5

Human Genetics

Volumn 97, Issue 2, 1996, Pages 163-170

  Besnard Guérin, Corinne ^a,b   Newsham, Irene ^a   Winqvist, Robert ^a,c   Cavenee, Webster K ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c OULU UNIVERSITY HOSPITAL   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CHROMOSOME 11P; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; EMBRYONAL RHABDOMYOSARCOMA; GENE LOSS; GENE MAPPING; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; HUMAN TISSUE; NEPHROBLASTOMA; NONHUMAN; PRIORITY JOURNAL;

BASE SEQUENCE; BECKWITH-WIEDEMANN SYNDROME; CELL LINE; CHILD; CHROMOSOMES, HUMAN, PAIR 11; GENE DELETION; GENES, WILMS TUMOR; GENETIC MARKERS; HETEROZYGOTE; HUMANS; HYBRID CELLS; KIDNEY NEOPLASMS; MOLECULAR SEQUENCE DATA; RHABDOMYOSARCOMA, EMBRYONAL; TRANSLOCATION, GENETIC; WILMS TUMOR;

EID: 0030027206     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02265259     Document Type: Article

References (52)

1. Ali IU, Lidereau R, Theillet C, Callahan R (1987) Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia. Science 238: 185-188
2. Bepler G, Garcia-Blanco MA (1994) Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell luns cancer. Proc Natl Acad Sci USA 91: 5513-5517
3. Bhattacharya S, Wilson TM, Wojciechowski AP, Volpe CP, Scott J (1991) Hypervariable polymorphism in the APOC3 gene. Nucleic Acids Res 19: 799
4. Bonetta L, Kuehn SE, Huang A, Law DJ, Kalikin LM, Koi M, Reeve AE, Brownstein BH, Yeger H, Williams BRG, Feinberg AP (1990) Wilms' tumor locus on 11p13 defined by multiple CpG island-associated transcripts. Science 250: 994-997
5. Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Duyk GM, Sheffield VC, Zhenyuan W, Murray JC (1994) Integrated human genome-wide maps constructed using the CEPH reference panel. Nat Genet 6: 391-393
6. Call KM, Glaser T, Ito CY, Buckler AJ, Pelletier J, Haber DA, Rose EA, Kral A, Yeger H, Lewis WH, Jones C, Housman DE (1990) Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell 60: 509-520
7. Cavenee WK, Dryja TP, Phillips RA, Benedict WF, Godbout R, Gallie BL, Murphree AL, Strong LC, White RL (1983) Expression of recessive alleles by chromosomal mechanisms in retinoblastoma, Nature 305: 779-784
8. Coppes MJ, Bonetta L, Huang A, Hoban P, Chilton-MacNeill S, Campbell CE, Weksberg R, Yeger H, Reeve AE, Williams BR. (1992) Loss of heterozygosity mapping in Wilms' tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination. Genes Chromosom Cancer 5: 326-34
9. Dao DD, Schroeder WT, Chao LY, Kikuchi H, Strong LC, Riccardi VM. Pathak S, Nichols WW, Lewis WH, Saunders GF (1987) Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor. Am J Hum Genet 41: 202-217
10. Dowdy SF, Fasching CL, Araujo D, Lai KM, Livanos E, Weissman BE, Stanbridge EJ (1991) Suppression of tumorigenicity in Wilms tumor by the p15.5-p14 region of chromosome 11. Science 254: 293-295
11. Fearon ER, Vogelstein B, Feinberg AP (1984) Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours. Nature 309: 176-178
12. Fearon ER, Feinberg AP, Hamilton SH, Vogelstein B (1985) Loss of genes on the short arm of chromosome 11 in bladder cancer. Nature 318: 377-380
13. Fults D, Petronio J, Noblett BD, Pedone CA (1992) Chromosome 11p15 deletions in human malignant astrocytomas and primitive neuroectodermal tumors. Genomics 14: 799-801
14. Garvin AJ, Re GG, Tamowski BI, Hazen-Martin DJ, Sens DA (1993) The G401 cell line, utilized for studies of chromosomal changes in Wilms' tumor, is derived from a rhabdoid tumor of the kidney. Am J Pathol 142: 375-380
15. Gessler M, Poustka A, Cavenee W, Neve RL, Orkin SH, Bruns GA (1990) Homozygous deletion in Wilms tumours of a zincfinger gene identified by chromosome jumping. Nature 343: 774-778
16. Gessler M, Konig A, Bruns GA (1992) The genomic organization and expression of the WT1 gene. Genomics 12: 807-813
17. Gessler M, Konig A, Arden K, Grundy P, Orkin S, Sallan S, Peters C, Ruyle S, Mandell J, Li F, Cavenee W, Bruns G (1994) Infrequent mutation of the WT1 gene in 77 Wilms' tumors. Hum Mutat 3: 212-222
18. 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
19. Grundy PE, Telzerow PE, Breslow N, Moksness J, Huff V, Paterson MC (1994) Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome. Cancer Res 54: 2331-2333
20. Hauge XY, Litt R, Litt M (1992) Dinucleotide repeat polymorphisms at the D11S439 and HBB loci. Hum Mol Genet 1: 548
21. Henry I, Grandjouan S, Couillin P, Barichard F, Huerre-Jeanpierre C, Glaser T, Philip T, Lenoir G, Chaussain JL, Junien C (1989) Tumor-specific loss of 11p15.5 alleles in dell 1p13 Wilms tumor and in familial adrenocortical carcinoma. Proc Natl Acad Sci USA 86: 3247-3251
22. Huff V, Compton DA, Chao LY, Strong LC, Geiser CF, Saunders GF (1988) Lack of linkage of familial Wilms' tumour to chromosomal band 11p13. Nature 336: 377-378
23. Jeanpierre C, Antignac C, Beroud C, Lavedan C, Henry I, Saunders G, Williams B, Glaser T, Junien C (1990) Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor. Genomics 7: 434-438
24. Kaneko Y, Takeda O, Homma C, Maseki N, Miyoshi H, Tsunematsu Y, Williams BG, Saunders GF, Sakurai M (1993) Deletion of WT1 and WIT1 genes and loss of heterozygosity on chromosome 11p in Wilms tumors in Japan. Jpn J Cancer Res 84: 616-624
25. Karnes PS, Tran TN, Cui MY, Bogenmann E, Shimada H, Ying KL (1991) Establishment of a rhabdoid tumor cell line with a specific chromosomal abnormality, 46,XY,t(11,22)(p15.5, q11.23). Cancer Genet Cytogenet 56: 31-38
26. Koi M, Johnson LA, Kalikin LM, Little PF, Nakamura Y, Feinberg AP (1993) Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11. Science 260: 361-364
27. Koufos A, Hansen MF, Lampkin BC, Workman ML, Copeland NG, Jenkins NA, Cavenee WK (1984) Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour. Nature 309: 170-172
28. Koufos A, Hansen MF, Copeland NG, Jenkins NA, Lampkin BC, Cavenee WK (1985) Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism. Nature 316: 330-334
29. Koufos A, Grundy P, Morgan K, Aleck KA, Hadro T, Lampkin BC, Kalbakji A, Cavenee WK (1989) Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. Am J Hum Genet 44: 711-719
30. Litt M, Kramer P, Hauge XY, Weber JL, Wang Z, Wilkie PJ, Holt MS, Mishra S, Donis-Keller H, Warnich L, Retief AE, Jones C, Weissenbach J (1993) A microsatellite-based index map of human chromosome 11. Hum Mol Genet 2: 909-913
31. Little MH, Thomson DB, Hay ward NK, Smith PJ (1988) Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome. Hum Genet 79: 186-189
32. Mannens M, Slater RM, Heyting C, Bliek J, Kraker J de, Coad N, de Pagter-Holthuizen P, Pearson PL (1988) Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours. Hum Genet 81: 41-48
33. Mannens M, Devilee P, Bliek J, Mandjes I, Kraker J de, Heyting C, Slater RM, Westerveld A. (1990) Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11. Cancer Res 50: 3279-3283
34. Maw MA, Grundy PE, Millow LJ, Eccles MR, Dunn RS, Smith PJ, Feinbera AP, LawDJ, Paterson MC, Telzerow PE, Callen DF, Thompson AD, Richards RI, Reeve AE (1992) A third Wilms' tumor locus on chromosome 16q. Cancer Res 52: 3094-3098
35. McNoe LA, Eccles MR, Reeve AE (1992) Dinucleotide repeat polymorphism at the D11S860 locus. Nucleic Acids Res 20: 1161
36. Newsham I, Daub D, Besnard-Guérin C, Cavenee W (1994) Molecular sublocalization and characterization of the 11.22 translocation breakpoint in a malignant rhabdoid tumor. Genomics 19: 433-440
37. Newsham I, Kindler-Röhrborn A, Daub D, Cavenee W (1995) A constitutional BWS-related t(11,16) chromosome translocation occuring in the same region of chromosome 16 implicated in Wilms' tumors. Genes Chromosom Cancer 12: 1-7
38. Nordenskjöld A, Hedborg F, Luthman H, Nordenskjold M (1993) Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite. Hum Genet 92: 296-298
39. Orkin SH, Goldman DS, Sallan SE (1984) Development of homozygosity for chromosome 11p markers in Wilms' tumour. Nature 309: 172-174
40. Ping AJ, Reeve AE, Law DJ, Young MR, Boehnke M, Feinberg AP (1989) Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am J Hum Genet 44: 720-723
41. Polymeropoulos MH, Xiao H, Rath DS, Merril CR (1991) Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH). Nucleic Acids Res 19: 3753
42. Redeker E, Hoovers JMN, Alders M, Moorsel CJA van, Ivens AC, Gregory S, Kalikin L, Bliek J, De Galan L, Bogaard R van den, Visser J, Voort R van der, Feinberg AP, Little PFR, Westerveld A, Mannens M (1994) An integrated physical map of 210 markers assigned to the short arm of human chromosome 11. Genomics 21: 538-550
43. Reeve AE, Housiaux PJ, Gardner RJ, Chewings WE, Grindley RM, Millow LJ (1984) Loss of a Harvey ras allele in sporadic Wilms' tumour. Nature 309: 174-176
44. Reeve AE, Sih SA, Raizis AM, Feinberg AP (1989) Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells. Mol Cell Biol 9: 1799-1803
45. Scrable HJ, Witte DP, Lampkin BC, Cavenee WK (1987) Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping. Nature 329: 645-647
46. Tadokoro K, Oki N, Sakai A, Fujii H, Ohshima A, Nagafuchi S, Inoue T, Yamada M (1993) PCR detection of 9 polymorphisms in the WT1 gene. Hum Mol Genet 2: 2205-2206
47. Tanci P, Genuardi M, Santini SA, Neri G (1992) PCR detection of an insertion/deletion polymorphism in intron 1 of the HRAS1 locus. Nucleic Acids Res 20: 1157
48. Wadey RB, Pal N, Buckle B, Yeomans E, Pritchard J, Cowell JK (1990) Loss of heterozygosity in Wilrns' tumour involves two distinct regions of chromosome 11. Oncogene 5: 901-907
49. Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millaseau P, Vaysseix G, Lathrop M (1992) A second-generation linkage map of the human genome. Nature 359: 794-801
50. Weissman BE, Saxon PJ, Pasquale SR, Jones GR, Geiser AG, Stanbridge EJ (1987) Introduction of a normal human chromosome 11 into a Wilms' tumor cell line controls its tumorigenic expression. Science 236: 175-180
51. Weksberg R, Teshima I, Williams BR, Greenberg CR, Pueschel SM, Chernos JE, Fowlow SB, Hoyme E, Anderson IJ. Whiteman DA, Fisher N, Squire J (1993) Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted. Hum Mol Genet 2: 549-556
52. Winqvist R, Mannermaa A, Alavaikko M, Blanco G, Taskinen PJ, Kivinierni H, Newsham I, Cavenee W (1993) Refinement of regional loss of heterozygosity for chromosome 11p15.5 in human breast tumors. Cancer Res 53: 4486-4488