Global correlation of genome and transcriptome changes in classical Hodgkin lymphoma

被引:18
作者
Kluiver, Joost
Kok, Klaas
Pfeil, Ines
de Jong, Debora
Blokzijl, Tjasso
Harms, Geert
van der Vlies, Pieter
Diepstra, Arjan
Atayar, Cigdem
Poppema, Sibrand
Kueppers, Ralf
van den Berg, Anke
机构
[1] Univ Groningen, Med Ctr, Dept Pathol & Lab Med, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Med Ctr, Dept Clin Genet, Groningen, Netherlands
[3] GSF, Inst Clin Mol Biol & Tumor Genet, Munich, Germany
[4] Univ Duisburg Essen, Inst Cell Biol Tumor Res, Essen, Germany
关键词
Hodgkin lymphoma; SAGE; array-based CGH; IRAK1; FSCN1;
D O I
10.1002/hon.804
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To identify genes involved in the pathogenesis of classical Hodgkin lymphoma (cHL), we performed serial analysis of gene expression (SAGE) and array-based comparative genomic hybridization (aCGH). Comparison of SAGE libraries of cHL cell lines L428 and L1236 with that of germinal centre B cells revealed consistent overexpression of only 14 genes. In contrast, 141 genes were downregulated in both cHL cell lines, including many B cell and HLA genes. aCGH revealed gain of 2p, 7p, 9p, 11q and Xq and loss of 4q and 11q. Eighteen percent of the differentially expressed genes mapped to regions with loss or gain and a good correlation was observed between underexpression and loss or overexpression and gain of DNA. Remarkably, gain of 2p and 9p did not correlate with increased expression of the proposed target genes c-REL and JAK2. Downregullation of many genes within the HLA region also did not correlate with loss of DNA. FSCN1 and IRAK1 mapping at genomic loci (7p and Xq) that frequently showed gain were overexpressed in cHL cell lines and might be involved in the pathogenesis of cHL. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:21 / 29
页数:9
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