Different chromosomal imbalances in metastasized and nonmetastasized tongue carcinomas identified by comparative genomic hybridization

被引:5
|
作者
Hannen, EJM
Macville, MVE
Wienk, SM
Slootweg, PJ
Manni, JJ
Hanselaar, AGJM
De Wilde, PCM
机构
[1] Univ Hosp Maastricht, Cytogenet Unit, Dept Clin Genet, NL-6202 AZ Maastricht, Netherlands
[2] Univ Hosp Maastricht, Dept Otorhinolaryngol Head & Neck Surg, NL-6202 AZ Maastricht, Netherlands
[3] Univ St Radboud, Ctr Med, Dept Pathol, NL-6500 HB Nijmegen, Netherlands
[4] Catharina Hosp Eindhoven, Dept Oral & Maxillofacial Surg, NL-5602 ZA Eindhoven, Netherlands
[5] Univ Utrecht, Ctr Med, Dept Pathol, NL-3508 GA Utrecht, Netherlands
关键词
human genome; comparative genomic hybridization; head and neck neoplasms; tongue neoplasms; metastasis;
D O I
10.1016/j.oraloncology.2003.09.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumors of different metastatic behavior possibly differ in genomic constitution. We identified molecular cytogenetic differences between a group of metastasized and nonmetastasized primary tongue tumors by comparative genomic hybridization. Most frequent chromosome copy number changes for metastasized and nonmetastasized tumors were +8q (100% and 71%, respectively) and +3q (56% and 43%, respectively). Metastasized tumors showed significantly more chromosome copy number changes than nonmetastasized tumors. High copy number gains were exclusively found in metastasized tumors for 3q23-qter, 5p, 12p and 13q2l-q22. Genomic imbalances occurring in metastasized tumors but not in nonmetastasized tumours were +7q2l (44%), +14q (33%), and -15q (33%). The genetic constitution of primary tongue tumors that metastasize differs from tongue tumors that do not metastasize. Our data, although obtained from a relative small group of tumors, spotlights copy number gain of chromosome region 7q21 as a potential marker for metastatic behavior. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:364 / 371
页数:8
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