Comparative genomic hybridization study of primary neuroblastoma tumors

被引:0
|
作者
Lastowska, M
Nacheva, E
McGuckin, A
Curtis, A
Grace, C
Pearson, A
Bown, N
机构
[1] UNIV NEWCASTLE, DEPT CHILD HLTH, NEWCASTLE UPON TYNE NE2 4AA, TYNE & WEAR, ENGLAND
[2] UNIV NEWCASTLE, CANC RES UNIT, NEWCASTLE UPON TYNE NE2 4AA, TYNE & WEAR, ENGLAND
[3] UNIV CAMBRIDGE, ADDENBROOKES HOSP, DEPT HAEMATOL, CAMBRIDGE CB2 1TN, ENGLAND
[4] ROYAL VICTORIA INFIRM, DEPT PATHOL, NEWCASTLE UPON TYNE NE1 4LP, TYNE & WEAR, ENGLAND
[5] DIGITAL SCI LTD, CAMBRIDGE, ENGLAND
[6] INST PAEDIAT, CLIN PAEDIAT HAEMATOL & ONCOL, POZNAN, POLAND
来源
GENES CHROMOSOMES & CANCER | 1997年 / 18卷 / 03期
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 1p (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. (C) 1997 Wiley-Liss, Inc.
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页码:162 / 169
页数:8
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