Neuroblastoma in two siblings supports the role of 1p36 deletion in tumor development

Cancer Genetics and Cytogenetics

Volumn 109, Issue 2, 1999, Pages 126-130

  Cunsolo, Crocifissa Lo ^a,c   Iolascon, Achille ^d   Cavazzana, Andrea ^e   Cusano, Roberto ^c   Strigini, Paolo ^b   Mazzocco, Katia ^a,c   Giordani, Lucia ^d   Massimo, Luisa ^c   De Bernardi, Bruno ^c   Conte, Massimo ^c   Tonini, Gian Paolo ^b  

^a ADVANCED BIOTECHNOLOGY CENTER   (Italy)

^b UNIVERSITY OF GENOA   (Italy)

^c G GASLINI INSTITUTE   (Italy)

^d UNIVERSITY OF BARI   (Italy)

^e SAN CAMILLO FORLANINI HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 1P; CHROMOSOME DELETION; FAMILIAL CANCER; FAMILY STUDY; FEMALE; GENE LOCUS; HUMAN; HUMAN CELL; MALE; NEURAL CREST CELL; NEUROBLASTOMA; PRIORITY JOURNAL; RECURRENT CANCER; SIBLING;

ABDOMINAL NEOPLASMS; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; GENES, MYC; GENETIC PREDISPOSITION TO DISEASE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LOSS OF HETEROZYGOSITY; MALE; MICROSATELLITE REPEATS; NEOPLASM STAGING; NEUROBLASTOMA; PEDIGREE; PREGNANCY;

EID: 0345130099     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(98)00154-X     Document Type: Article

References (24)

1. Dodge H.J., Benner M.C. Neuroblastoma of adrenal medulla in siblings. Rocky Mt Med J. 42:1945;35-38.
2. Chatten J., Voorhess M.L. Familial neuroblastoma. N Engl J Med. 277:1967;1230-1236.
3. Kushner B.H., Helson H. Monozygotic siblings discordant for neuroblastoma. etiologic implications J Pediatr. 107:1985;405-409.
4. Kushner B.H., Gilbert F., Helson L. Familial neuroblastoma. Cancer. 57:1986;1887-1893.
5. Gilbert F., Balaban G., Moorhead P., Bianchi D., Schlesinger H. Abnormalities of chromosome 1p in human neuroblastoma tumors and cell lines. Cancer Genet Cytogent. 7:1982;33-42.
6. Fong C., Dracopoli N.C., White P.S., Merrill P.T., Griffith R.C., Housman D.E., Brodeur M.G. Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastoma. correlation with N-myc amplification Proc Natl Acad Sci USA. 86:1989;3753-3757.
7. Schleiermacher G., Peter M., Michon J., Hugot J.P., Viehl P., Zucker J.M., Magdelénat H., Thomas G., Delattre O. Two distinct regions on the short arm of chromosome 1 in neuroblastoma. Genes Chromosom Cancer. 10:1994;275-281.
8. Caron H., Peter M., van Sluis P., Speleman F., de Kraker J., Laureys G., Michon J., Brugieres L., Voute P.A., Westerveld A., Slater R., Delattre O., Versteeg R. Evidence for two tumor suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma. one probably imprinted, another associated with N-myc amplification Hum Mol Genet. 4:1995;535-539.
9. Kaghad M., Bonnet H., Yang A., Creancier L., Biscan J.-C., Valent A., Minty A., Chalon P., Lelias J.-M., Dumont X., Ferrara P., McKeon F., Caput D. Monoallelic expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers. Cell. 90:1997;800-819.
10. Maris J.M., Kyemba S.M., Rebbeck T.R., White P.S., Sulman E.P., Jensen S.J., Allen C., Biegel A.J., Yanofsky R.A., Feldman G.L., Broduer G.M. Familial predisposition to neuroblastoma does not map to chromosome band 1p36. Cancer Res. 56:1996;3421-3425.
11. Shimada H., Chatten J., Newton J., Sachs W., Hamoudi N., Chiba T., Marsden H., Misugi K. Histopathologic prognostic factors in neuroblastic tumors. definition of subtypes of ganglioneuroblastoma and an age-linked classification of neuroblastomas J Natl Cancer Inst. 73:1984;405-416.
12. Brodeur G.M., Pritchard J., Berthold F., Carlsten N.L.T., Castel V., Castleberry R.P., De Bernardi B., Evans A.E., Favrot M., Hedborg F., Kaneko M., Kamshead J., Lampert F., Lee R.E.J., Look A., Pearson A.D.J., Philip T., Roald B., Sawada T., Seeger R.C., Tsuchida Y., Voute P.A. Revisions of the international criteria for neuroblastoma diagnosis, staging and response to treatment. J Clin Oncol. 11:1993;1466-1477.
13. Pinkel D., Straume T., Gray J.W. Cytogenetic analysis using quantitative, high sensitivity, fluorescence hybridization. Proc Natl Acad Sci USA. 83:1986;2934-2938.
14. Sambrook J., Fritsch E.F., Maniatis T. Molecular Cloning. A Laboratory Manual. ed 2:1989;Cold Spring Harbor Laboratory, Cold Spring Harbor, NY.
15. Southern E.M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 98:1975;503-517.
16. Martine P., Michon J., Vielh P., Neuenschwander S., Nakamura Y., Sonsino E., Zucker J.M., Vergnaud G., Thomas G., Delattre O. PCR assay for chromosome 1p deletion in small neuroblastoma samples. Int J Cancer. 52:1992;544-548.
17. Zhuang Z., Bertheau P., Emmert-Buck M.R., Liotta L.A., Gnarra J., Lnehan W.M., Lubensky I.A. A microdissection technique for archival DNA. analysis of specific cell population in lesions <1 mm in size Am J Pathol. 146:1995;620-625.
18. Caron H., Van Sluis P., De Kraker J., Bökkerink J., Egeler M., Laureys G., Slater R., Westerveld A., Voûte P.A., Versteeg R. Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma. N Engl J Med. 334:1996;225-230.
19. Weiss W.A., Aldape K., Mohapatra G., Feuerstein B.G., Bishop J.M. Targeted expression of MYCN causes neuroblastoma in transgenic mice. EMBO J. 11:1997;2985-2995.
20. Iolascon A., Lo Cunsolo C., Giordani L., Cusano R., Mazzocco K., Boumgartner M., Ghisellini P., Faienza M.F., Boni L., De Bernardi B., Conte M., Romeo G., Tonini G.P. Interstitial and large chromosome 1p deletion occurs in localized and disseminated neuroblastomas and predict an unfavourable outcome. Cancer Lett. 130:1998;83-92.
21. Knudson A.G. Jr., Meadows A.T. Developmental genetics of neuroblastoma. J Natl Cancer Inst. 57:1976;675-682.
22. Srivastan E.S., Murali V., Seeger R.C. Loss of heterozygosity for alleles on chromosome 11q and 14, in neuroblastoma. Prog Clin Biol Res. 366:1991;91-98.
23. Caron H., Van Sluis P., Buschman R., Pereira do Tanque R., Maes P., Becks L., de Kraker J., Voûte P.A., Vergnaud G., Westrveld A., Slater R., Versteeg R. Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus. Hum Genet. 97:1996;834-837.
24. Altura R.A., Maris J.M., Li H., Boyett J.M., Brodeur G.M., Look A.T. Novel regions of chromosomal loss in familial neuroblastoma by comparative genomic hybridization. Genes Chromosom Cancer. 19:1997;176-184.