Comparative genomic hybridization detects specific cytogenetic abnormalities in pediatric ependymomas and choroid plexus papillomas

Cancer Genetics and Cytogenetics

Volumn 136, Issue 2, 2002, Pages 121-125

  Grill, Jacques ^a   Avet Loiseau, Hervé ^b   Lellouch Tubiana, Arielle ^c   Sévenet, Nicolas ^d   Terrier Lacombe, Marie José ^a   Vénuat, Anne Marie ^a   Doz, François ^d   Sainte Rose, Christian ^c   Kalifa, Chantal ^a   Vassal, Gilles ^a  

^a INSTITUT GUSTAVE ROUSSY   (France)

^b INSTITUT DE BIOLOGIE   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d INSTITUT CURIE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CHOROID PLEXUS PAPILLOMA; CHROMOSOME 10Q; CHROMOSOME 12Q; CHROMOSOME 15; CHROMOSOME 22Q; CHROMOSOME 3P; CHROMOSOME 6Q; CHROMOSOME 7; CHROMOSOME 9; CHROMOSOME ABERRATION; CHROMOSOME LOSS; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; CYTOGENETICS; EPENDYMOMA; FEMALE; GENE MUTATION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INFANT; MALE; PATHOGENESIS; PRIORITY JOURNAL; PROGNOSIS; RELAPSE; TUMOR GROWTH; TUMOR SUPPRESSOR GENE;

BRAIN NEOPLASMS; CHILD; CHILD, PRESCHOOL; CHOROID PLEXUS NEOPLASMS; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; EPENDYMOMA; HUMANS; INFANT; MALE; NUCLEIC ACID HYBRIDIZATION; PAPILLOMA;

EID: 18644367887     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(02)00516-2     Document Type: Article

References (24)

1. Hamilton R.L., Pollack I. The molecular biology of ependymoma. Brain Pathol. 7:1997;807-822.
2. Ebert C., von Haken M., Meyer-Puttlitz B., Wiestler O.D., Reifenberger G., Pietsch T., von Deimling A. Molecular genetic analysis of ependymal tumors. NF2 mutations and chromosome 22q loss occur preferentially in intramedullary spinal ependymomas. Am J Pathol. 155:1999;627-632.
3. Hirose Y., Aldape K., Bollen A., James C.D., Brat D., Lamborn K., Berger M., Feuerstein B.G. Chromosomal abnormalities subdivide ependymal tumors into clinically relevant groups. Am J Pathol. 158:2001;1137-1143.
4. Applegate G.L., Marymont M.H. Intracranial ependymomas. a review Cancer Invest. 16:1998;588-593.
5. Grill J., Le Deley M.C., Gambarelli D., Raquin M.A., Couanet D., Pierre-Kahn A., Habrand J.L., Doz F., Frappaz D., Gentet J.C., Edan C., Chastagner P., Kalifa C. Post-operative chemotherapy without irradiation for ependymoma in children under five years of age. A multicenter trial of the French Society of Pediatric Oncology (SFOP). J Clin Oncol. 19:2001;1288-1296.
6. Watanabe K., Tachibana O., Sata K., Yonekawa Y., Kleihues P., Ohgaki K. Overexpression of the EGF receptor and p53 mutations are mutually exclusive in the evolution of primary and secondary glioblastomas. Brain Pathol. 6:1996;217-223.
7. Kramer D.L., Parmiter A.H., Rorke L.B., Sutton L.N., Biegel J.A. Molecular cytogenetic studies of pediatric ependymomas. J Neurooncol. 37:1998;25-33.
8. Mazewski C., Soukup S., Ballard E., Gotwals B., Lampkin B. Karyotype studies in 18 ependymomas with literature review of 107 cases. Cancer Genet Cytogenet. 113:1999;1-8.
9. Neumann E., Kalousek D.K., Norman M.G., Steinbok P., Cochrane D.D., Goddard K. Cytogenetic analysis of 109 pediatric central nervous system tumors. Cancer Genet Cytogenet. 71:1993;40-49.
10. Reardon D.A., Entrekin R.E., Sublett J., Ragsdale S., Li H., Boyett J., Kepner J.L., Look A.T. Chromosome arm 6q loss is the most common recurrent autosomal alteration detected in primary pediatric ependymoma. Genes Chromosomes Cancer. 24:1999;230-237.
11. Pencalet P., Sainte-Rose C., Lellouch-Tubiana A., Kalifa C., Brunelle F., Sgouros S., Meyer P., Cinalli G., Zerah M., Pierre-Kahn A., Renier D. Papillomas and carcinomas of the choroid plexus in children. J Neurosurg. 88:1998;521-528.
12. Chow E., Reardon D.A., Shah A.B., Jenkins J.J., Langston J., Heideman R.L., Sanford R.A., Kun L.E., Merchant T.E. Pediatric choroid plexus neoplasms. Int J Radiat Oncol Biol Phys. 44:1999;249-254.
13. Figarella-Branger D., Lepidi H., Poncet C., Gambarelli D., Bianco N., Rougon G., Pellissier J.F. Differential expression of cell adhesion molecules (CAM), neural CAM and epithelial cadherin in ependymomas and choroid plexus tumors. Acta Neuropathol. 89:1995;248-257.
14. Bhattacharjee M.B., Armstrong D.D., Vogel H., Cooley L.D. Cytogenetic analysis of 120 primary pediatric brain tumors and literature review. Cancer Genet Cytogenet. 97:1997;39-53.
15. Avet-Loiseau H., Venuat A.M., Terrier-Lacombe M.J., 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. 79:1999;1843-1847.
16. Sévenet N., Lellouch-Tubiana A., Schofield D., Hoang-Xuan K., Gessler M., Birnbaum D., Jeanpierre C., Jouvet A., Delattre O. Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations. Hum Mol Genet. 8:1999;2359-2368.
17. Nicholson J.C., Ross F.M., Kohler J.A., Ellison D.W. Comparative genomic hybridization and histological variation in primitive neuroectodermal tumours. Br J Cancer. 80:1999;1322-1331.
18. Nishizaki T., Harada K., Kubota H., Ozaki S., Ito H., Sasaki K. Genetic alterations in pediatric medulloblastomas detected by comparative genomic hybridization. Pediatr Neurosurg. 31:1999;27-32.
19. Reardon D.A., Michalkiewicz E., Boyett J.M., Sublett J.E., Entrekin R.E., Ragsdale S.T., Valentine M.B., Behm F.G., Li H., Heideman R.L., Kun L.E., Shapiro D.N., Look A.T. Extensive genomic abnormalities in childhood medulloblastoma by comparative genomic hybridization. Cancer Res. 57:1997;4042-4047.
20. Russo C., Pellarin M., Tingby O., Bollen A.W., Lamborn K.R., Mohapatra G., Collins V.P., Feuerstein B.G. Comparative genomic hybridization in patients with supratentorial and infratentorial primitive neuroectodermal tumors. Cancer. 86:1999;331-339.
21. Bigner S.H., McLendon R.E., Fuchs H., McKeever P.E., Friedman H.S. Chromosomal characteristics of childhood brain tumors. Cancer Genet Cytogenet. 97:1997;125-134.
22. Jenkins R.B., Kimmel D.W., Moertel C.A., Schultz C.G., Scheithauer B.W., Kelly P.J., Dewald G.W. A cytogenetic study of 53 human gliomas. Cancer Genet Cytogenet. 39:1989;253-279.
23. Myiakawa A., Ichimura K., Schmidt E.E., Varmeh-Ziaie S., Collins V.P. Multiple deleted regions on the long arm of chromosome 6 in astrocytic tumours. Br J Cancer. 82:2000;543-549.
24. Burger P.C., Yu I.T., Tihan T., Friedman H.S., Strother D.R., Kepner J.L., Duffner P.K., Kun L.E., Perlman E.J. Atypical teratoid/rhabdoid tumor of the central nervous system. a highly malignant tumor of infancy and childhood frequently mistaken for medulloblastoma: a Pediatric Oncology Group study Am J Surg Pathol. 22:1998;1083-1092.