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Comparative genomic hybridization study of primary neuroblastoma tumors
Author(s) -
Łastowska Maria,
Nacheva Elizabeth,
McGuckin Angela,
Curtis Ann,
Grace Colin,
Pearson Andrew,
Bown Nick
Publication year - 1997
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/(sici)1098-2264(199703)18:3<162::aid-gcc2>3.0.co;2-#
Subject(s) - comparative genomic hybridization , neuroblastoma , primary (astronomy) , biology , computational biology , medicine , cancer research , genetics , genome , gene , physics , astronomy , cell culture
Neuroblastoma tumors show a complex interaction of genetic abnormalities, among which some are of significant prognostic importance; however, analysis of chromosome changes in this tumor is often unsuccessful. Twenty primary tumors were studied by comparative genomic hybridization (CGH), and abnormalities were found in 19. While these changes included deletions of chromosome arm lp (45%) and MYCN oncogene amplification (30%), gains of chromosome 17 material were much more frequent (75%). We also found evidence in two cases of a new amplification site at band 2p23. Genes Chromosom. Cancer 18:162–169, 1997. © 1997 Wiley‐Liss, Inc.