Genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumours of the central nervous system

Histopathology

Volumn 47, Issue 6, 2005, Pages 631-637

  Inda, M M ^a   Perot, C ^b   Guillaud Bataille, M ^b   Danglot, G ^b   Rey, J A ^c   Bello, M J ^c   Fan, X ^d   Eberhart, C ^d   Zazpe, I ^e   Portillo, E ^e   Tunon T ^e   Martinez Penuela J M ^e   Bernheim, A ^b   Castresana, Javier S ^a  

^a UNIVERSITY OF NAVARRA   (Spain)

^b INSTITUT GUSTAVE ROUSSY   (France)

^c HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

^d JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e Universidad Pública de Navarra   (Spain)

Author keywords

CGH; Embryonal tumour; i(17q); Infratentorlal PNET; Medulloblastoma; Primitive neuroectodermal tumour; Supratentorial PNET

Indexed keywords

ARTICLE; BRAIN TUMOR; CEREBELLUM TUMOR; CHROMOSOME 10; CHROMOSOME 16P; CHROMOSOME 17Q; CHROMOSOME 19P; CHROMOSOME 4Q; CHROMOSOME 7; CHROMOSOME ANALYSIS; CHROMOSOME LOSS; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; GENE AMPLIFICATION; GENE EXPRESSION PROFILING; GENE FREQUENCY; GENETIC HETEROGENEITY; HUMAN; HUMAN TISSUE; ISOCHROMOSOME; NEUROECTODERM TUMOR; PRIORITY JOURNAL;

EID: 28844494157     PISSN: 03090167     EISSN: 13652559     Source Type: Journal    
DOI: 10.1111/j.1365-2559.2005.02304.x     Document Type: Article

References (23)

1. Nicholson JC, Ross FM, Kohler JA, Ellison DW. Comparative genomic hybridization and histological variation in primitive neuroectodermal tumours. Br. J. Cancer 1999; 80; 1322-1331.
2. Russo C, Pellarin M, Tingby O et al. Comparative genomic hybridization in patients with supratentorial and infratentorial primitive neuroectodermal tumors. Cancer 1999; 86; 331-339.
3. Pruchon E, Chauveinc L, Sabatier L et al. A cytogenetic study of 19 recurrent gliomas. Cancer Genet. Cytogenet. 1994; 76; 85-92.
4. Burnett ME, White EC, Sih S, von Haken MS, Cogen PH. Chromosome arm 17p deletion analysis reveals molecular genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumors of the central nervous system. Cancer Genet. Cytogenet. 1997; 97; 25-31.
5. Biegel JA. Cytogenetics and molecular genetics of childhood brain tumors. Neuro-Oncol. 1999; 1; 139-151.
6. Bigner SH, Mark J, Friedman HS, Biegel JA, Bigner DD. Structural chromosomal abnormalities in human medulloblastoma. Cancer Genet. Cytogenet. 1988; 30; 91-101.
7. Kallioniemi A, Kallioniemi OP, Sudar D et al. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 1992; 258; 818-821.
8. du Manoir S, Speicher MR, Joos S et al. Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. Hum. Genet. 1993; 90; 590-610.
9. Kallioniemi OP, Kallioniemi A, Piper J et al. Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors. Genes Chromosomes Cancer 1994; 10; 231-243.
10. Forozan F, Karhu R, Kononen J, Kallioniemi A, Kallioniemi OP. Genome screening by comparative genomic hybridization. Trends Genet. 1997; 13; 405-409.
11. Bentz M, Plesch A, Stilgenbauer S, Dohner H, Lichter P. Minimal sizes of deletions detected by comparative genomic hybridization. Genes Chromosomes Cancer 1998; 21; 172-175.
12. Reardon DA, Jenkins JJ, Sublett JE, Burger PC, Kun LK. Multiple genomic alterations including N-myc amplification in a primary large cell medulloblastoma. Pediatr. Neurosurg. 2000; 32; 187-191.
13. Scheurlen WG, Schwabe GC, Joos S, Mollenhauer J, Sorensen N, Kühl J. Molecular analysis of childhood primitive neuroectodermal tumors defines markers associated with poor outcome. J. Clin. Oncol. 1998; 16; 2478-2485.
14. Nicholson J, Wickramasinghe C, Ross F, Crolla J, Ellison D. Imbalances of chromosome 17 in medulloblastomas determined by comparative genomic hybridisation and fluorescence in situ hybridisation. Mol. Pathol. 2000; 53; 313-319.
15. Avet-Loiseau H, Venuat AM, Terrier-Lacombe MJ, Lellouch-Tubiana A, Zerah M, Vassal G. Comparative genomic hybridization detects many recurrent imbalances in central nervous system primitive neuroectodermal tumours in children. Br. J. Cancer 1999; 79; 1843-1847.
16. Reardon DA, Michalkiewicz E, Boyett JM et al. Extensive genomic abnormalities in childhood medulloblastoma by comparative genomic hybridization. Cancer Res. 1997; 57; 4042-4047.
17. Schutz BR, Scheurlen W, Krauss J et al. Mapping of chromosomal gains and losses in primitive neuroectodermal tumors by comparative genomic hybridization. Genes Chromosomes Cancer 1996; 16; 196-203.
18. Gilhuis HJ, Anderl KL, Boerman RH et al. Comparative genomic hybridization of medulloblastomas and clinical relevance: eleven new cases and a review of the literature. Clin. Neurol. Neurosurg. 2000; 102; 203-209.
19. Kraus JA, Koch A, Albrecht S, Von Deimling A, Wiestler OD, Pietsch T. Loss of heterozygosity at locus F13B on chromosome 1q in human medulloblastoma. Int. J. Cancer 1996; 67; 11-15.
20. Tong CY, Hui AB, Yin XL et al. Detection of oncogene amplifications in medulloblastomas by comparative genomic hybridization and array-based comparative genomic hybridization. J. Neurosurg. 2004; 100; 187-193.
21. Vagner-Capodano AM, Gentet JC, Gambarelli D et al. Cytogenetic studies in 45 pediatric brain tumors. Pediatr. Hematol. Oncol. 1992; 9; 223-235.
22. Fuller GN, Bigner SH. Amplified cellular oncogenes in neoplasms of the human central nervous system. Mutat. Res. 1992; 276; 299-306.
23. Fruhwald MC, O'Dorisio MS, Rush LJ et al. Gene amplification in PNETs/medulloblastomas: mapping of a novel amplified gene within the MYCN amplicon. J. Med. Genet. 2000; 37; 501-509.