No preferential parent of origin for the isochromosome 17q in childhood primitive neuroectodermal tumor (medulloblastoma)

Genes Chromosomes and Cancer

Volumn 18, Issue 2, 1997, Pages 143-146

  Biegel, Jaclyn A ^a,b   Wentz, Erica ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADOLESCENT; ARTICLE; CARCINOGENESIS; CHILD; CHROMOSOME 17Q; CHROMOSOME DELETION; CLINICAL ARTICLE; FEMALE; HUMAN; ISOCHROMOSOME; MALE; MEDULLOBLASTOMA; NEUROECTODERM TUMOR; PARENT; POSTERIOR CRANIAL FOSSA TUMOR; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; HUMANS; ISOCHROMOSOMES; MALE; MEDULLOBLASTOMA; NEUROECTODERMAL TUMORS, PRIMITIVE;

EID: 0031023313     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199702)18:2<143::AID-GCC9>3.0.CO;2-2     Document Type: Article

References (19)

1. Biegel JA, Rorke LB, Packer RJ, Sutton LN, Schut L, Bonner K, Emanuel BS (1989) Isochromosome 17q in primitive neuroectodermal tumors of the central nervous system. Genes Chromosom Cancer 1:139-147.
2. Bieget JA, Burk CD, Barr FG, Emanuel BS (1992) Evidence for a 17p tumor related locus disnnct from p55 in pediaitric central nervous system primitive neuroctodermal tumors. Cancer Res 52:3391-3395.
3. Biegel JA, Rorke LB, Janss AJ, Sutton LN, Parmiter AH (1995) Isochrosomes 17q demonstrated by interphase FISH in primitive neuroectodermal tumors of the central nervous system. Genes Chromosom Cacer 14:85-96.
4. Blacker H, Rasheed BKA, McLendon RE, Friedman HS, Surinder K, Batra SK, Fuchs HE, Bigner SH (1996) Microsatellite unalysis of childhood brain rumors. Genes Chromosom Cancer 15:54-63.
5. Caron H, van Sluis P, van Hoeve M, de Kraker J, Bras J, Slater R, Mannens M, Voute PA, Westerveld A, Versteeg R (1993) Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification. Nat Genet 4:187-190.
6. Chens JM, Hiemstra JL, Schneider SS, Naumova A, Cheung N-KV, Cohn SL, Diller L, Sapienza C, and Brodeur GM (1995) Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomas. Nat Gener 4:191-194.
7. Cogen PH (1991) Progostic significance in molecular genetic markers in childhood brain tumors. Pediatr Neurosurg 17:245-250.
8. Feinberg AP (1995) Genomic imprinting and gene activation in cancer, Nat Genet 4:110-113.
9. Felix CA, Slave I, Dunn M, Strauss EA, Biegel JA (1995) Germline and somatric p53 gene mutations in pediatric brain tumors. Med Pediatr Oncol 25:431-436.
10. Gerken SC, Albertsen H, Elsner T, Ballard L, Holik P, Lawrence E, Moore M, Zhao X, White R (1995) A strategy for constructing high-resolution genetic maps of the human genome: A genetic map of chromosome 17p, ordered with meiotic breakpoint-mapping panels. Am J Hum C Genet 56:484-499.
11. Ledbetter DH, Enjgel E (1995) Uniperental disomy in humans: Development of an imprinting map and its implications for prenatal diagnosis. Hum Mol Genet 4:1757-1764.
12. McDonald JD, Daneshvar L, Willert JR, Matsumura K, Waldman F, Cogen PH (1994) Physical mapping of chromosome 17p13.3 in the region of a putative tumor suppressor gene important in medullo-blastoma. Genomics 12:229-232.
13. Raffel C, Gilles FE, Weinberg KI (1990) Reduction to homozygosity and gene amplification in central nervous system primitive neuroectodermal tumors of childhood. Cancer Res 50:587-591.
14. Raffel C, Thomas GA, Tishler DM, Lassoff S, Allen JC (1993) Absence of p53 mutations in childhood central nervous system primitive neuroectodermal tumors. Neurosurgery 33:301-306.
15. Sapienza C (1992) Genome imprinting and cancer genetics. Semin Cancer Biol 3:151-158.
16. Saylor RL, Sidransky D, Friedman HS, Bigner SH, Bigner DD, Vogelstein B, Brodeur GM (1991) Infrequent p53 gene mutations in medulloblastomas. Cancer Res 51:4721-4723.
17. Slave I, Rodriguez IR, Mazuruck K, Chader GJ, Biegel J (1995) Loss of hetererozygosity detected by single strand conformation polymorphism analysis of PEDF in central nervous system primitive neuroectodermal tumors. Proc Am Assoc Cancer Res 36:545.
18. Stack M, Crichton D, Santibanez-Koref M (1994) Two dinucleotide repeat polymorphisms at 17p13. Hum Mol Genet 3:1443.
19. Wales MM, Biel MA, Deiry WE, Nelkin BD, Issa J-P, Cavenee WJ, Baylin SB (1995) p53 activates expression of HIC-1, a new candidate tumour suppressor gene on 17p13.3. Nat Med 1:570-577.