Genetic alterations on Chromosome 19, 20, 21, 22, and X detected by loss of heterozygosity analysis in retinoblastoma

Molecular Vision

Volumn 9, Issue , 2003, Pages 502-507

  Huang, Qing ^a,b   Choy, Kwong Wai ^a   Cheung, Kin Fai ^a   Lam, D S C ^a   Fu, Wei Ling ^b   Pang, Chi Pui ^a  

^a CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^b THIRD MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

ALLELE; ARTICLE; CARCINOGENESIS; CELL SUBPOPULATION; CHROMOSOME 19; CHROMOSOME 20; CHROMOSOME 21; CHROMOSOME 22; CHROMOSOME TRANSLOCATION 13; CLINICAL ARTICLE; CONTROLLED STUDY; GENE FREQUENCY; GENE LOCUS; GENE LOSS; GENE MUTATION; GENETIC ANALYSIS; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; HUMAN TISSUE; MICRODISSECTION; MICROSATELLITE INSTABILITY; MICROSATELLITE MARKER; PROMOTER REGION; RETINOBLASTOMA; X CHROMOSOME;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN; CHROMOSOMES, HUMAN, PAIR 19; CHROMOSOMES, HUMAN, PAIR 20; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 22; CHROMOSOMES, HUMAN, X; DNA, NEOPLASM; FEMALE; HUMANS; INFANT; LOSS OF HETEROZYGOSITY; MALE; MICROSATELLITE REPEATS; RETINAL NEOPLASMS; RETINOBLASTOMA;

EID: 0347300613     PISSN: 10900535     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (38)

1. Sluyser M. Molecular biology of cancer genes. New York: Ellis Horwood; 1990.
2. Jackson AL, Loeb LA. The contribution of endogenous sources of DNA damage to the multiple mutations in cancer. Mutat Res 2001; 477:7-21.
3. Knudson AG Jr. Mutation and cancer: statistical study of retinoblastoma. Proc Natl Acad Sci U S A 1971; 68:820-3.
4. DiCiommo D, Gallie BL, Bremner R. Retinoblastoma: the disease, gene and protein provide critical leads to understand cancer. Semin Cancer Biol 2000; 10:255-69.
5. Horsthemke B. Genetics and cytogenetics of retinoblastoma. Cancer Genet Cytogenet 1992; 63:1-7.
6. Cowell JK, Hogg A. Genetics and cytogenetics of retinoblastoma. Cancer Genet Cytogenet 1992; 64:1-11.
7. Oliveros O, Yunis E. Chromosome evolution in retinoblastoma. Cancer Genet Cytogenet 1995; 82:155-60.
8. Pogosianz HE, Kuznetsova LE. Nonrandom chromosomal changes in retinoblastomas. Arch Geschwulstforsch 1986; 56:135-43.
9. Squire J, Phillips RA, Boyce S, Godbout R, Rogers B, Gallie BL. Isochromosome 6p, a unique chromosomal abnormality in retinoblastoma: verification by standard staining techniques, new densitometric methods, and somatic cell hybridization. Hum Genet 1984; 66:46-53.
10. Sivakumaran TA, Ghose S, Kumar H, Singha U, Kucheria K. Absence of pericentromeric heterochromatin (9qh-) in a patient with bilateral retinoblastoma. Acta Genet Med Gemellol (Roma) 1997; 46:193-8.
11. Lee WH, Murphree AL, Benedict WF. Expression and amplification of the N-myc gene in primary retinoblastoma. Nature 1984; 309:458-60.
12. Arheden K, Tommerup N, Mandahl N, Heim S, Winther J, Jensen OA, Prause JU, Mitelman F. Amplification of the human putative oncogene INT1 in primary retinoblastoma tumors. Cytogenet Cell Genet 1988; 48:174-7.
13. Imbert I, Coignet LJ, Pellestor F. 6p abnormalities and TNF-alpha over-expression in retinoblastoma cell line. Cancer Genet Cytogenet 2001; 128:141-7.
14. Chen D, Pajovic S, Duckett A, Brown VD, Squire JA, Gallie BL. Genomic amplification in retinoblastoma narrowed to 0.6 megabase on chromosome 6p containing a kinesin-like gene, RBKIN. Cancer Res 2002; 62:967-71.
15. Kato MV, Shimizu T, Ishizaki K, Kaneko A, Yandell DW, Toguchida J, Sasaki MS. Loss of heterozygosity on chromosome 17 and mutation of the p53 gene in retinoblastoma. Cancer Lett 1996; 106:75-82.
16. Hovig E, Andreassen A, Fangan BM, Borresen AL. A TP53 mutation detected in cells established from an osteosarcoma, but not in the retinoblastoma of a patient with bilateral retinoblastoma and multiple primary osteosarcomas. Cancer Genet Cytogenet 1992; 64:178-82.
17. Hida T, Kinoshita Y, Matsumoto R, Suzuki N, Tanaka H. Bilateral retinoblastoma with a 13qXp translocation. J Pediatr Ophthalmol Strabismus 1980; 17:144-6.
18. Nichols WW, Miller RC, Sobel M, Hoffman E, Sparkes RS, Mohandas T, Veomett I, Davis JR. Further observations on a 13qXp translocation associated with retinoblastoma. Am J Ophthalmol 1980; 89:621-7.
19. Ejima Y, Sasaki MS, Kaneko A, Tanooka H, Hara Y, Hida T, Kinoshita Y. Possible inactivation of part of chromosome 13 due to 13qXp translocation associated with retinoblastoma. Clin Genet 1982; 21:357-61.
20. Laquis SJ, Rodriguez-Galindo C, Wilson MW, Fleming JC, Haik BG. Retinoblastoma in a patient with an X;13 translocation and facial abnormalities consistent with 13q-syndrome. Am J Ophthalmol 2002; 133:285-7.
21. Mateu E, Sanchez F, Najera C, Beneyto M, Castell V, Hernandez M, Serra I, Prieto F. Genetics of retinoblastoma: a study. Cancer Genet Cytogenet 1997; 95:40-50.
22. Jones C, Booth C, Rita D, Jazmines L, Brandt B, Newlan A, Horsthemke B. Bilateral retinoblastoma in a male patient with an X; 13 translocation: evidence for silencing of the RB1 gene by the spreading of X inactivation. Am J Hum Genet 1997; 60:1558-62.
23. Stambolian D, Sellinger B, Derrington D, Sargent R, Emanuel BS. Cytogenetic and molecular investigation of a balanced Xq13q translocation in a patient with retinoblastoma. Am J Med Genet 1992; 42:771-6.
24. Ponzio G, Savin E, Cattaneo G, Ghiotti MP, Marra A, Zuffardi O, Danesino C. Translocation X;13 in a patient with retinoblastoma. J Med Genet 1987; 24:431-4.
25. Cross HE, Hansen RC, Morrow G 3rd, Davis JR. Retinoblastoma in a patient with a 13qXp translocation. Am J Ophthalmol 1977; 84:548-54.
26. Kajii T, Tsukahara M, Fukushima Y, Hata A, Matsuo K, Kuroki Y. Translocation (X;13) (p11.21;q12.3) in a girl with incontinentia pigmenti and bilateral retinoblastoma. Ann Genet 1985; 28:219-23.
27. Goodarzi G, Mashimo T, Watabe M, Cuthbert AP, Newbold RF, Pai SK, Hirota S, Hosobe S, Miura K, Bandyopadhyay S, Gross SC, Balaji KC, Watabe K. Identification of tumor metastasis suppressor region on the short arm of human chromosome 20. Genes Chromosomes Cancer 2001; 32:33-42.
28. MacGrogan D, Alvarez S, DeBlasio T, Jhanwar SC, Nimer SD. Identification of candidate genes on chromosome band 20q12 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines. Oncogene 2001; 20:4150-60.
29. Cleton-Jansen AM, Callen DF, Seshadri R, Goldup S, Mccallum B, Crawford J, Powell JA, Settasatian C, van Beerendonk H, Moerland EW, Smit VT, Harris WH, Millis R, Morgan NV, Barnes D, Mathew CG, Cornelisse CJ. Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions. Cancer Res 2001; 61:1171-7.
30. Berney CR, Fisher RJ, Yang J, Russell PJ, Crowe PJ. Genomic alterations (LOH, MI) on chromosome 17q21-23 and prognosis of sporadic colorectal cancer. Int J Cancer 2000; 89:1-7.
31. Zhou CZ, Peng ZH, Zhang F, Qiu GQ, He L. Loss of heterozygosity on long arm of chromosome 22 in sporadic colorectal carcinoma. World J Gastroenterol 2002; 8:668-73.
32. Sakata K, Tamura G, Nishizuka S, Maesawa C, Suzuki Y, Iwaya T, Terashima M, Saito K, Satodate R. Commonly deleted regions on the long arm of chromosome 21 in differentiated adenocarcinoma of the stomach. Genes Chromosomes Cancer 1997; 18:318-21.
33. Workman ML, Soukup SW. Chromosome features of two retinoblastomas. Cancer Genet Cytogenet 1984; 12:365-70.
34. Mohandas T, Sparkes RS, Shapiro LJ. Genetic evidence for the inactivation of a human autosomal locus attached to an inactive X chromosome. Am J Hum Genet 1982; 34:811-7.
35. Modrich P, Lahue R. Mismatch repair in replication fidelity, genetic recombination, and cancer biology. Annu Rev Biochem 1996; 65:101-33.
36. Thomas DC, Umar A, Kunkel TA. Microsatellite instability and mismatch repair defects in cancer. Mutat Res 1996; 350:201-5.
37. Maehara Y, Oda S, Sugimachi K. The instability within: problems in current analyses of microsatellite instability. Mutat Res 2001; 461:249-63.
38. Zheng L, Flesken-Nikitin A, Chen PL, Lee WH. Deficiency of Retinoblastoma gene in mouse embryonic stem cells leads to genetic instability. Cancer Res 2002; 62:2498-502.