Transformation of follicular lymphoma to diffuse large cell lymphoma is associated with a heterogeneous set of DNA copy number and gene expression alterations

被引:173
作者
Martinez-Climent, JA
Alizadeh, AA
Segraves, R
Blesa, D
Rubio-Moscardo, F
Albertson, DG
Garcia-Conde, J
Dyer, MJS
Levy, R
Pinkel, D
Lossos, IS
机构
[1] Univ Valencia, Hosp Clin, Dept Hematol & Med Oncol, Valencia 46010, Spain
[2] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA USA
[3] Stanford Univ, Sch Med, Dept Med, Stanford, CA USA
[4] Univ Calif San Francisco, Comprehens Canc Ctr, San Francisco, CA USA
[5] Univ Calif San Francisco, Canc Res Inst, San Francisco, CA USA
[6] Univ Leicester, Dept Haematol, Leicester, Leics, England
关键词
D O I
10.1182/blood-2002-07-2119
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genomic aberrations in a series of paired biopsy samples from patients who presented initially with follicle center lymphoma (FCL) and subsequently transformed to diffuse large B-cell lymphoma (DLBCL) were measured by array comparitive genomic hybridization (CGH). The consequences of these aberrations on gene expression were determined by comparison with expression analysis on these specimens using cbNA microarrays. A heterogeneous pattern of acquired genomic abnormalities was observed upon transformation, some of which Were recurrent in small subsets of patients. Some, of the genomic aberration acquired upon transformation, such as gain/amplification of 1q21-q24., 2p16 (REL/BCL11A gene loci), 3qV-q29 (including the BCL6 locus), 7q11.2-q22.1 12pter-q12, 18q21 (including the BCL2 locus) and Xq, and deletion of 6q22-q24, 13q14-q21 and 17p13 (P53 locus) have been previously implicated in the FCL/DLBCL pathogenesis. 16 addition, novel genomic imbalances not previously reported in association with FCL transformation, such as overrepresentation of 4p12-pter, 5p12-p15, 6p12.3-p21, 9p23,9q13 q31,16q, 17q21, and loss of 1p36.3, 4021-q23, 5q21-q23, 9q31-qter, 11q24-q25, and 15q23, were identified. We observed a differential expression profile of many genes within regions of gain and deletion upon transformation, including novel target genes associated with FCL transformation. However, other genes did not show deregulated expression despite their location within these areas. In summary, the combination of array CGH and expression analysis provides a more comprehensive picture of the transformation of FCL to DLBCL. This process is associated with the acquisition of a variable spectrum of genomic imbalances affecting recurrent chromosomal areas that harbor overexpressed or underexpressed genes targeted upon transformation. (C) 2003 by The American Society of Hematology.
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页码:3109 / 3117
页数:9
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