Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumour

British Journal of Cancer

Volumn 78, Issue 9, 1998, Pages 1181-1187

  Grundy, R G ^a,c   Pritchard, J ^a,b   Scambler, P ^a   Cowell, J K ^a,d  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b GREAT ORMOND STREET HOSPITAL   (United Kingdom)

^c BIRMINGHAM CHILDREN S HOSPITAL   (United Kingdom)

^d LERNER RESEARCH INSTITUTE   (United States)

Author keywords

Chromosome 16; Loss of heterozygosity; Prognosis; Wilms' tumour

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; CHROMOSOME 16Q; GENE LOSS; GENETIC POLYMORPHISM; HETEROZYGOSITY LOSS; HISTOLOGY; HUMAN; HUMAN CELL; HUMAN TISSUE; NEPHROBLASTOMA; PRIORITY JOURNAL; PROGNOSIS;

EID: 0031754683     PISSN: 00070920     EISSN: None     Source Type: Journal    
DOI: 10.1038/bjc.1998.651     Document Type: Article

References (37)

1. Austruy E, Candon S, Henry I, Gyapay G, Tournade M-F, Mannens M, Callen D, Junien C and Jeanpierre C (1995) Characterisation of regions of chromosome 12 and 16 involved in nephroblastoma tumongenesis. Genes Chrom Cancer 14: 285-294
2. Beckwith JB, Kiviat NB and Bonadio JF (1990) Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor. Pediatr Pathol 10: 1-36
3. Bergerheim USR, Kunimi K, Collins VP and Ekman P (1991) Detection mapping of chromosomes 8, 10 and 16 in human prostatic carcinoma. Genes Chrom Cancer 3: 215-220
4. Cavenee, WK, Dryja TP, Phillips RA, Benedict WF, Godbout R, Gallie BL, Murphree AL, Strong LC and White RL (1983) Expression of recessive alleles by chromosomal mechanisms in retinoblastoma. Nature 305: 779-784
5. Coppes MJ, Bonetta L, Huang A, Hoban P, Chilton-Macneill S, Campbell E, Weksberg R, Yeger H, Reeve AE and Williams BRG (1992) Loss of heterozygosity mapping in Wilms' tumour indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination. Genes Chrom Cancer 5: 326-334
6. D'angio GJ, Evans A, Breslow N, Beckwith B, Bishop H, Farewell V, Goodwin W, Leape L, Palmer N, Sink SL, Sutow W, Tefft M and Wolff J. (1981) The treatment of Wilins' tumour: results of the second National Wilms' Tumour study. Cancer 47: 2302-2311
7. D'angio GJ, Breslow N, Beekwith JB, Evans A, Baum E, Delorimier A, Fernback D, Hrahovsky E, Jones B, Kelalis P, Othersen HB, Tefft M and Thomas PRM (1989) Treatment of Wilms' tumour: results of the third National Wilms' tumour study. Cancer 64: 349-360
8. Doggett NA, Goodwin LA, Tesmer JG, Meincke LJ, Brece DC, Clark LM, Altherr MR, Ford AA, Chi, H-C, Marrone BL, Longmire JL, Lane SA, Whitmore SA, Lowenstein MG, Sutheralnd RD, Mundt MO, Knill EH, Bruno WJ, Macken CA, Torney DC, WU, J-R, Griffith J, Sutherland GR, Deaven LL, Callen DF and Moyzis RK (1995) An integrated physical map of human chromosome 16. Nature 377: 355-365
9. Dorion-Bonnet, F, Mutalen, S, Holstein I and Longy M. (1995) Allelic imbalance study of 16q in human primary breast carcinimas using microsatellite markers. Genes Chrom Cancer 14: 171-181
10. Douglass EC, Rowe ST, Valentine M, Parham D, Meyer WH and Thompson, EI (1990) A second non-random translocation der (16)t(1;16)(q21;q13) in Ewings sarcoma and peripheral neuroectodermal tumour. Cytogenet Cell Genet 53: 87-90
11. Fujimori M, Tokino T, Hino O, Kitagawa T, Imamura T, Okamoto E, Mitsunobu M, Nakagama H, Hurada H, Yagura M, Matsubara K and Nakumura Y(1991) Allotype study of hepatocellular carcinoma. Cancer Res 51: 89-93
12. Goorin AM, Chauvenet AR and Perez-atayde AR (1990) Initial congestive cardiac failure six to ten years after doxorubicin therapy for childhood cancer. J Pediatr 116: 144
13. Grundy PE, Telzerow PE, Breslow N, Moksness J, Huff V and Paterson MC (1994) Loss heterozygosity for chromosomes 16q and 1p in Wilms' tumours predicts an adverse outcome. Cancer Res 54: 2331-2333
14. Gyapay G, Morisette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, Bernardi G, Lathrop M and Weissenbach J (1994) The 1993-94 Genethon human genetic linkage map. Nature Genet 7: 246-299
15. Kaneko Y, Homma C, Maseki N, Sakurai M and Hata J (1991) Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors. Cancer Res 51: 5937-5942
16. Knudson AG and Strong LC (1972) Mutation and cancer: a model for Wilms' tumour of the kidney. J Natl Cancer Inst 48: 313-324
17. Koufos A, Grundy P, Morgan K, Aleck KA, Hadro R, Lampkin BC, Kalbakji A and Cavenee WK (1989) Familial Wiedemann-Beckwith syndrome and a second Wilms' tumour locus both map to 11p15.5. Am J Hum Genet 44: 711-719
18. Kozman HM, Keith TP, Donis-Keller H, White RL, Wissenbaeh J, Dean M, Vergnaud G, Kidd K, Gusella J, Royle, NJ, Sutherland GR and Mulley JC (1995) The CEPH consortium linkage map of human chromosome 16. Genomics 25: 44-58
19. Mannens M, Hoovers JMN, Redeker E, Verjaal M, Feinberg A, Little P, Boavida M, Coad N, Steenman M, Bliek J, Slater RM, DE Boer EG, John R, Cowel, L JK, Junien C, Henry I, Tomerup N, Niikawa N, Weksberg R, Pueschel SM, Leschot NJ and Westerveld, A (1994) Parental imprinting of human chromosome region 11p15.4-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia. Eur J Hum Genet 2: 3-23
20. Matthew P, Douglass EC, Jones D, Valentine M, Valentine V, Rowe S and Shapiro DN (1996) Der(16) t (1:16)(q21;q13) in Wilms' tumour: friend or foe. Med Ped Oncol 23: 3-7
21. Maw M, Grundy P, Millow L, Eccles M, Dun R, Smith P, Feinberg A, Law D, Patterson M, Telzerow P, Callem D, Thompson A, Richards R and Reeve A (1992) A third tumour locus on chromosome 16q. Cancer Res 52: 3094-3098
22. Mugneret F, Lizard S, Aurias A and Turc-Carel C (1988) Chromosomes in Swings sarcoma. II. Non-random additional changes, trisomy 8 and der(16)t(1;16). Cancer Genet Cytogenet 32: 239-245
23. Newsham I, Kindler-Rohrborn A, Daub D and Cavenee W (1995) A constitutional BWS-related t(1;16) chromosome translocation occuring in the same region of chromosome 16 implicated in Wilms' tumour. Genes Chrom Cancer 12: 1-7
24. Park S, Bernard A, Bove K, Sens DA, Hazen-Martin DJ, Garvin AJ and Haber DA (1993) Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour. Nature Genet 5: 363-367
25. Ping AJ, Reeve AE, Law DJ, Young MR, Boehnke M and Feinberg AP (1989) Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am J Hum Genet 44: 720-723
26. Pritchard J, Imeson J, Barnes J, Cotterill S, Gough D, Marsden HB, Morris-Jones P and Pearson D (1995) Results of the United Kingdom children's cancer study group first Wilms' tumour study. J Clin Oncol 13: 124-133
27. Redeker E, Lip KVD, Bliek J, Spelman F, Kraker JD, Voute PA, Westerveld A and Mannens M (1996) Allele Loss Patterns in Childhood Kidney Tumours. University of Amsterdam: Amsterdam
28. Sato T, Tanigami A, Yamakawa K, Akiyama F, Kasumi F, Sakamoto G and Nakamura Y (1990) Allotype of breast carcinoma: Cumulative allele losses promote tumour progression in primary breast cancer. Cancer Res 50: 7184-7189
29. Slater RM and Mannens M (1992) Cytogenetics and molecular genetics of Wilms' tumor of childhood. Cancer Genet Cytogenet 61: 111-121
30. Solis V, Pritchard J and Cowell JK (1988) Cytogenetic changes in Wilms' tumors. Cancer Genet Cytogenet 34: 223-234
31. Sorenson K, Levitt G, Sebag-Montefiore D, Bull C and Sullivan I (1995) Cardiac function in Wilms' tumour survivors. J Clin Oncol 13: 1546-1556
32. Thomas GA and Raffel C (1991) Loss of heterozygosity on 6q, 16q and 17p in human central nervous system primitive neuroectodermal tumours. Cancer Res 51: 639-643
33. Tsuda H, Zhang W, Shimosato Y, Yokota Y, Terada M, Sugimura, T, Miyamura T and Hirohashi S (1990) Allele loss on chromosome 16 associated with progression of human hepatocellular carcinoma. Proc Natl Acad Sci USA 87: 6791-6794
34. Wadey RB, Pal NP, Buckle B, Yeomans E, Pritchard J and Cowell JK (1990) Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome II. Oncogene 5: 901-907
35. Wang-Wuu S, Soukup S, Bove K, Gotwals B and Lampkin B (1990) Chromosome analysis of 31 Wilms' tumors. Cancer Res 50: 2786-2793
36. Weksberg R, Teshima I, Williams BGR, Greenberg CR, Pueschel SM, Chernos JE, Fowlow SB, Hoyme E, Anderson IJ, Whiteman DAH, Fisher N and Squire J (1993) Molecular characterisation 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
37. Wiedemann HR (1983) Tumours and hemihypertrophy associated with Wiedemann-Beckwith syndrome. Eur J Pediatr 141: 129