Distinct types of primary cutaneous large B-cell lymphoma identified by gene expression profiling

被引:183
作者
Hoefnagel, JJ
Dijkman, R
Basso, K
Jansen, PM
Hallermann, C
Willemze, R
Tensen, CP
Vermeer, MH
机构
[1] Leiden Univ, Med Ctr, Dept Dermatol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Pathol, NL-2300 RC Leiden, Netherlands
[3] Columbia Univ, Inst Canc Genet, New York, NY USA
[4] Univ Hosp Gottingen, Dept Dermatol, Gottingen, Germany
关键词
D O I
10.1182/blood-2004-04-1594
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the European Organization for Research and Treatment of Cancer (EORTC) classification 2 types of primary cutaneous large B-cell lymphoma (PCLBCL) are distinguished: primary cutaneous follicle center cell lymphomas (PCFCCL) and PCLBCL of the leg (PCLBCL-leg). Distinction between both groups is considered important because of differences in prognosis (5-year survival > 95% and 52%, respectively) and the first choice of treatment (radiotherapy or systemic chemotherapy, respectively), but is not generally accepted. To establish a molecular basis for this subdivision in the EORTC classification, we investigated the gene expression profiles of 21 PCLBCLs by oligonucleotide microarray analysis. Hierarchical clustering based on a B-cell signature (7450 genes) classified PCLBCL into 2 distinct subgroups consisting of, respectively, 8 PCFCCLs and 13 PCLBCLs-leg. PCLBCLs-leg showed increased expression of genes associated with cell proliferation; the proto-oncogenes Pim-1, Pim-2, and c-Myc; and the transcription factors Mum1/IRF4 and Oct-2. In the group of PCFCCL high expression of SPINK2 was observed. Further analysis suggested that PCFCCLs and PCLBCLs-leg have expression profiles similar to that of germinal center B-cell-like and activated B-cell-like diffuse large B-cell lymphoma, respectively. The results of this study suggest that different pathogenetic mechanisms are involved in the development of PCFCCLs and PCLBCLs-leg and provide molecular support for the subdivision used in the EORTC classification.
引用
收藏
页码:3671 / 3678
页数:8
相关论文
共 51 条
[31]  
LIDA S, 1997, NAT GENET, V17, P226
[32]   Comparative genomic hybridization analysis of primary cutaneous B-cell lymphomas: Identification of common genomic alterations in disease pathogenesis [J].
Mao, X ;
Lillington, D ;
Child, F ;
Russell-Jones, R ;
Young, B ;
Whittaker, S .
GENES CHROMOSOMES & CANCER, 2002, 35 (02) :144-155
[33]   MOLECULAR-CLONING OF LSIRF, A LYMPHOID-SPECIFIC MEMBER OF THE INTERFERON REGULATORY FACTOR FAMILY THAT BINDS THE INTERFERON-STIMULATED RESPONSE ELEMENT (ISRE) [J].
MATSUYAMA, T ;
GROSSMAN, A ;
MITTRUCKER, HW ;
SIDEROVSKI, DP ;
KIEFER, F ;
KAWAKAMI, T ;
RICHARDSON, CD ;
TANIGUCHI, T ;
YOSHINAGA, SK ;
MAK, TW .
NUCLEIC ACIDS RESEARCH, 1995, 23 (12) :2127-2136
[34]   Requirement for the Transcription Factor LSIRF/IRF4 for Mature B and T Lymphocyte Function [J].
Mittrucker, Hans-Willi ;
Matsuyama, Toshifumi ;
Grossman, Alex ;
Kundig, Thomas M. ;
Potter, Julia ;
Shahinian, Arda ;
Wakeham, Andrew ;
Patterson, Bruce ;
Ohashi, Pamela S. ;
Mak, Tak W. .
JOURNAL OF IMMUNOLOGY, 2017, 199 (11) :3717-3720
[35]   ORGANIZATION AND SEQUENCE OF THE GENE ENCODING THE HUMAN ACROSIN-TRYPSIN INHIBITOR (HUSI-II) [J].
MORITZ, A ;
GRZESCHIK, KH ;
WINGENDER, E ;
FINK, E .
GENE, 1993, 123 (02) :277-281
[36]   Mutations of the BCL6 proto-oncogene disrupt its negative autoregulation in diffuse large B-cell lymphoma [J].
Pasqualucci, L ;
Migliazza, A ;
Basso, K ;
Houldsworth, J ;
Chaganti, RSK ;
Dalla-Favera, R .
BLOOD, 2003, 101 (08) :2914-2923
[37]   Primary cutaneous large B-cell lymphoma of the leg: Histogenetic analysis of a controversial clinicopathologic entity [J].
Paulli, M ;
Viglio, A ;
Vivenza, D ;
Capello, D ;
Rossi, D ;
Riboni, R ;
Lucioni, M ;
Incardona, P ;
Boveri, E ;
Bellosta, M ;
Orlandi, E ;
Borroni, G ;
Lazzarino, M ;
Berti, E ;
Alessi, E ;
Magrini, U ;
Gaidano, G .
HUMAN PATHOLOGY, 2002, 33 (09) :937-943
[38]   The use of molecular profiling to predict survival after chemotherapy for diffuse large-B-cell lymphoma [J].
Rosenwald, A ;
Wright, G ;
Chan, WC ;
Connors, JM ;
Campo, E ;
Fisher, RI ;
Gascoyne, RD ;
Muller-Hermelink, HK ;
Smeland, EB ;
Staudt, LM .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (25) :1937-1947
[39]   Cell cycle deregulation in B-cell lymphomas [J].
Sánchez-Beato, M ;
Sánchez-Aguilera, A ;
Piris, MA .
BLOOD, 2003, 101 (04) :1220-1235
[40]  
SANTUCCI M, 1991, CANCER, V67, P2311, DOI 10.1002/1097-0142(19910501)67:9<2311::AID-CNCR2820670918>3.0.CO