Acquired homozygosity (isodisomy) of chromosome 3 in uveal melanoma

Cancer Genetics and Cytogenetics

Volumn 102, Issue 1, 1998, Pages 40-45

  White, Valerie A ^a,b   McNeil, B Kelly ^a   Horsman, Douglas E ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b VANCOUVER GENERAL HOSPITAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 3; CHROMOSOME ABERRATION; CYTOGENETICS; EYE TUMOR; HETEROZYGOSITY LOSS; HOMOZYGOSITY; HUMAN; HUMAN CELL; HUMAN TISSUE; MELANOMA; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; UVEA TUMOR;

AUTORADIOGRAPHY; CHROMOSOMES, HUMAN, PAIR 3; HUMANS; KARYOTYPING; LOSS OF HETEROZYGOSITY; MELANOMA; MONOSOMY; UVEAL NEOPLASMS;

EID: 0032054429     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(97)00290-2     Document Type: Article

References (32)

1. Prescher G, Bornfeld N, Becher R (1990): Nonrandom chromosomal abnormalities in primary uveal melanoma. J Natl Cancer Inst 82:1765-1769.
2. Sisley K, Cottam DW, Rennie IG, Parsons MA, Potter AM, Potter GW, Rees RC (1992): Non-random abnormalities of chromosomes 3, 6, and 8 associated with posterior uveal melanoma. Genes Chromosom Cancer 5:197-200.
3. Dahlenfors R, Tornqvist G, Wettrell K, Mark J (1993): Cytogenetical observations in nine ocular malignant melanomas. Anticancer Res. 13:1415-1420.
4. Horsman DE, White VA (1993): Cytogenetic analysis of uveal melanoma: Consistent occurrence of monosomy 3 and trisomy 8q. Cancer 71:811-819.
5. Wiltshire RN, Einer VM, Dennis T, Vine AK, Trent JM (1993): Cytogenetic analysis of posterior uveal melanoma. Cancer Genet Cytogenet 66:47-53.
6. Singh AD, Boghosian-Sell L, Wary KK, Shields CL, De Potter P, Donoso LA, Shields JA, Cannizzaro LA (1994): Cytogenetic findings in primary uveal melanoma. Cancer Genet Cytogenet 72:109-115.
7. Prescher G, Bornfeld N, Friedrichs W, Seeber S, Becher R (1995): Cytogenetics of twelve cases of uveal melanoma and patterns of nonrandom anomalies and isochromsome formation. Cancer Genet Cytogenet 80:40-46.
8. White VA, McNeil BK, Thiberville L, Horsman DE (1996): Acquired homozygosity (isodisomy) of chromosome 3 during clonal evolution of a uveal melanoma: Association with morphologic heterogeneity. Genes Chromosom Cancer 15:138-143.
9. O'Connell P, Leach RJ, Rains D, Taylor T, Garcia D, Ballard L, Holik P, Weissenbach J, Sherman S, Wilkie P, Weber JL, Naylor S (1994): A PCR-based genetic map for human chromosome 3. Genomics 24:557-567.
10. Sakurai A, Bell GI, DeGroot LJ (1991): Dinucleotide repeat polymorphism in the human thyroid hormone receptor β gene (THRB) on chromosome 3. Nucleic Acids Res 19:6661.
11. Hudson TJ, Engelstein M, Lee MK, Ho EC, Rubenfield MJ, Adams CP, Housman DE, Dracopoli NC (1992): Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms. Genomics 13:622-629.
12. Schmidt L, Li H, Wei M, Lerman MI, Zbar B, Tory K (1993): Six dinucleotide microsatellite polymorphisms on human chromosome 3. Hum Mol Genet 2:817-818.
13. Thiberville L, Bourguignon J, Metayer J, Bost F, Diarra-Mehrpour M, Bignon J, Lam S, Martin JP, Nouvel G (1995): Frequency and prognostic evaluation of 3p21-22 allelic losses in non-small cell lung cancer. Int J Cancer 64:371-377.
14. Goradia TM, Stanton VP, Xiangfeng C, Aburitani H, Li H, Lange K, Housman DE, Arnheim N (1991): Ordering three DNA polymorphisms on human chromosome 3 by sperm typing. Genomics 10:748-755.
15. Jones MH, Yamakawa K, Nakamura Y (1992): Isolation and characterization of 19 dinucleotide repeat polymorphisms on chromosome 3p. Hum Mol Genet 1:131-133.
16. Weber JL, May PE (1989): Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am J Hum Genet 44:388-396.
17. Weber JL, May PE, Patterson D, Drabkin H, Killary AM (1991): Dinucleotide repeat polymorphism at the D3S196 locus. Nucleic Acids Res 18:4635.
18. Granqvist M, Xiang K, Seino M, Fukomoto H, Bell GI (1991): Dinucleotide repeat polymorphism in human GLUT2/liver facilitative glucose transporter gene on chromosome 3. Nucleic Acids Res 19:4791.
19. Peng H, Bailey D, Bronson D, Goss PE, Hogg D (1995): Loss of heterozygosity of tumor suppressor genes in testis cancer. Cancer Res 55:2871-2875.
20. Cavenee WK, Dryja TP, Phillips RA, Benedict WF, Godbout R, Gallie BR, Murphree AL, Strong LC, White RL (1983): Expression of recessive alleles by chromosomal mechanisms in retinoblastoma. Nature 305:779-784.
21. Mukai S, Dryja TP (1986): Loss of alleles at polymorphic loci on chromosome 2 in uveal melanoma. Cancer Genet Cytogenet 22:45-53.
22. Horsthemke B, Prescher G, Bornfeld N, Becher R (1992): Loss of chromosome 3 alleles and multiplication of chromosome 8 alleles in uveal melanoma. Genes Chromosom Cancer 4:217-221.
23. Sisley K, Curtis D, Rennie IG, Rees RC (1993): Loss of heterozygosity of the thyroid hormone receptor B in posterior uveal melanoma. Melanoma Res 3:457-461.
24. Soparker CN, O'Brien JM, Albert DM (1993): Investigation of the role of the ras protooncogene mutation in human uveal melanomas. Invest Ophthalmol Visual Sci 34:2203-2209.
25. Mooy CM, Luyten GPM, de Jong PTVM, Luider TM, Stijnen T, van de Ham F, van Vroonhoven CCJ, Bosman FT (1995): Immunohistochemical and prognostic analysis of apoptosis and proliferation in uveal melanoma. Am J Pathol 147:1097-1104.
26. Jay V, Qiong Y, Hunter WS, Zielenska M (1996): Expression of bcl-2 in uveal malignant melanoma. Arch Pathol Lab Med 120:497-498.
27. Hemminki A, Peltomaki P, Mecklin J, Jarvinen H, Salovaara R, Nystrom-Lahti M, de la Chapelle A, Aaltonen LA (1994): Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer. Nat Genet 8:405-410.
28. Thomas JH (1995): Genomic imprinting proposed as a surveillance mechanism for chromosome loss. Proc Natl Acad Sci USA 92:480-482.
29. Feinberg AP, Kalikin LM, Johnson LA, Thompsom JS (1994): Loss of imprinting in human cancer. Cold Spring Harbor Symp Quant Biol 59:357-364.
30. Buchhagen DL, Qui L, Etkind P (1994): Homozygous deletion, rearrangement and hypermethylation implicate chromosome region 3p14.3-3p21.3 in sporadic breast-cancer development. Int J Cancer 57:473-479.
31. Zbar B (1995): Von Hippel-Lindau disease and sporadic renal cell carcinoma. Cancer Surv 25:219-232.
32. Virgilio L, Shuster M, Gollin SM, Veronese ML, Ohta M, Heubner K, Croce CM (1996): FHIT gene alterations in head and neck squamous cell carcinomas. Proc Natl Acad Sci USA 93:9770-9775.