Molecular analysis of the region of distal 1p commonly deleted in neuroblastoma

European Journal of Cancer

Volumn 33, Issue 12, 1997, Pages 1957-1961

  White, P S ^a   Maris, J M ^a   Sulman, E P ^a   Jensen, S J ^a   Kyemba, S M ^a   Beltinger, C P ^a   Allen, C ^a   Kramer, D L ^a   Biegel, J A ^a   Brodeur, G M ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

1p36; Loss of heterozygosity; Neuroblastoma; Tumour suppressor

Indexed keywords

CANCER SURVIVAL; CHROMOSOME 1P; CHROMOSOME ABERRATION; CONFERENCE PAPER; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE DISRUPTION; GENETIC ANALYSIS; GENETIC HETEROGENEITY; HUMAN; HUMAN CELL; NEUROBLASTOMA; PRIORITY JOURNAL; PROGNOSIS; TUMOR SUPPRESSOR GENE;

CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; CONSENSUS SEQUENCE; GENES, TUMOR SUPPRESSOR; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LOSS OF HETEROZYGOSITY; MULTIVARIATE ANALYSIS; NEUROBLASTOMA; PROGNOSIS; PROPORTIONAL HAZARDS MODELS; RISK FACTORS; TUMOR CELLS, CULTURED;

EID: 0031408114     PISSN: 09598049     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0959-8049(97)00311-0     Document Type: Conference Paper

References (28)

1. Brodeur G. M., Fong C. T. Molecular biology and genetics of human neuroblastoma. Cancer Genet Cytogenet. 41:1989;153-174.
2. Takayama H, Suzuki T, Mugishima H, et al. Deletion mapping of chromosomes 14q and 1p in human neuroblastoma. Oncogene 1992, 7, 1185-1189.
3. Schleiermacher G, Peter M, Michon J, et al. Two distinct deleted regions on the short arm of chromosome 1 in neuroblastoma. Genes Chromosom Cancer 1994, 10, 275-281.
4. Takeda O, Homma C, Maseki N, et al. There may be two tumor suppressor genes on chromosome arm 1p closely associated with biologically distinct subtypes of neuroblastoma. Genes Chromosom Cancer 1994, 10, 30-39.
5. Caron H, Peter M, van Sluis P, et al. Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification. Hum Mol Genet 1995, 4, 535-539.
6. Martinsson T., Sjoberg R. M., Hedborg F., Kogner P. Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms. Cancer Res. 55:1995;5681-5686.
7. White PS, Maris JM, Beltinger C, et al. A region of consistent deletion in neuroblastoma maps within 1p36.2-.3. Proc Natl Acad Sci USA 1995, 92, 5520-5524.
8. Laureys G., Speleman F., Opdenakker G., Leroy J. Constitutional translocation t(1;17)(p36;q12-21) in a patient with neuroblastoma. Genes Chromosom Cancer. 2:1990;252-254.
9. Biegel JA, White PS, Marshall HN, et al. Constitutional 1p36 deletion in a child with neuroblastoma. Am J Hum Genet 1993, 52, 176-182.
10. Brodeur G. M., Green A. A., Hayes F. A. Cytogenetic studies of primary human neuroblastomas. Prog Cancer Res Ther. 12:1980;73-80.
11. van Roy N, Laureys G, Cheng NC, et al. 1;17 translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell lines. Genes Chromosom Cancer 1994, 10, 103-114.
12. Bader S. A., Fasching C., Brodeur G. M., Stanbridge E. J. Dissociation of suppression of tumorigenicity and differentiation in vitro effected by transfer of single human chromosomes into human neuroblastoma cells. Cell Growth Differ. 2:1991;245-255.
13. Maris JM, White PS, Beltinger CP, et al. Significance of chromosome 1p loss of heterozygosity in neuroblastomas. Cancer Res 1995, 55, 4664-4669.
14. Maris JM, Jensen SJ, Sulman EP, et al. Cloning, chromosomal localization, physical mapping and genomic characterization of HKR3. Genomics 1996, 35, 289-298.
15. Dib C, Fauré S, Fizames C, et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 1996, 380, 152-154.
16. Matise T. C., Perlin M., Chakravarti A. Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map. Nature Genet. 6:1994;384-390.
17. Murray JC, Buetow KH, Weber JL, et al. A comprehensive human linkage map with centimorgan density. Science 1994, 265, 2049-2054.
18. Hudson TJ, Stein LD, Gerety SS, et al. An STS-based map of the human genome. Science 1995, 270, 1945-1954.
19. Albertsen H. M., Abderrahim H., Cann H. M., Dausset J., Le Paslier D., Cohen D. Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents. Proc Natl Acad Sci USA. 87:1990;4256-4260.
20. Gyapay G, Morissette J, Vignal A, et al. The 1993-94 Genethon human genetic linkage map. Nature Genet 1994, 7, 246-339.
21. Fong CT, Dracopoli NC, White PS, et al. Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification. Proc Natl Acad Sci USA 1989, 86, 3753-3757.
22. Fong CT, White PS, Peterson K, et al. Loss of heterozygosity for chromosomes 1 or 14 defines subsets of advanced neuroblastomas. Cancer Res 1992, 52, 1780-1785.
23. Gehring M., Berthold F., Edler L., Schwab M., Amler L. The 1p deletion is not a reliable marker for the prognosis of patients with neuroblastoma. Cancer Res. 55:1995;5366-5369.
24. Caron H, van Sluis P, de Kraker J, et al. Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma. New Engl J Med 1996, 334, 225-230.
25. Aso T., Mokady N., Haque D. Assignment of a human gene encoding the 110-kDa subunit of general transcription factor elongin (SIII) to chromosome 1p36.1. Genomics. 30:1995;393-394.
26. Collins A., Keats B. J., Dracopoli N., Shields D. C., Morton N. E. Integration of gene maps: chromosome 1. Proc Natl Acad Sci USA. 89:1992;4598-4602.
27. van der Drift P, Chan A, Laureys G, et al. Balanced translocation in a neuroblastoma patient disrupts a cluster of small nuclear RNA U1 and tRNA genes in chromosomal band 1p36. Genes Chromosom Cancer 1995, 14, 35-42.
28. Beltinger CP, White PS, Maris JM, et al. Physical mapping and genomic structure of the human TNFR2 gene. Genomics 1996, 35, 94-100.