Comparative genomic hybridization reveals population-based genetic alterations in hepatoblastomas

被引:22
|
作者
Gray, SG
Kytölä, S
Matsunaga, T
Larsson, C
Ekström, TJ
机构
[1] Karolinska Inst, Dept Clin Neurosci, CMM, Expt Alcohol & Drug Addict Res Sect,Lab Mol Dev &, S-17176 Stockholm, Sweden
[2] Karolinska Hosp, Dept Mol Med, Endocrine Tumor Unit, S-17176 Stockholm, Sweden
[3] Chiba Univ, Sch Med, Dept Pediat Surg, Chuo Ku, Chiba 2600856, Japan
关键词
hepatoblastoma; cytogenetics; Caucasian; Japanese; amplification;
D O I
10.1054/bjoc.2000.1390
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatoblastoma is a malignant paediatric liver tumour. in order to approach the genetic background of this malignancy we have screened a panel of eighteen cases from Europe and Japan for chromosomal imbalances using comparative genomic hybridization (CGH). The most frequent losses included chromosomal regions 13q21-q22 (28%) and 9p22-pter (22%), while the most frequent gains occurred on 2q23-q24 (33%), 20q (28%) and 1q24-q25 (28%), A significant difference in CGH alterations between the tumours from patients of Caucasian and Japanese was revealed where toss of 13q was found only in the Japanese samples. In conclusion, the findings indicate several candidate regions for suppressor genes and oncogenes potentially involved in the hepatoblastomas of different ethnic origin, (C) 2000 Cancer Research Campaign.
引用
收藏
页码:1020 / 1025
页数:6
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