Gene expression profile of Ewing sarcoma cell lines differing in their EWS-FLI1 fusion type

被引:12
作者
Bandrés, E
Malumbres, R
Escalada, A
Cubedo, E
González, I
Honorato, B
Zarate, R
García-Foncillas, J
de Alava, E
机构
[1] Univ Navarra, Ctr Appl Med Res, CIMA, Lab Pharmacogenom, Pamplona 31008, Spain
[2] Univ Navarra, Ctr Appl Med Res, Canc Res Program, Pamplona 31008, Spain
[3] Univ Salamanca, Canc Res Ctr, Lab Mol Pathol, E-37008 Salamanca, Spain
关键词
Ewing sarcoma cell lines; EWS-FLI-1; microarray; gene expression profile;
D O I
10.1097/01.mph.0000184576.38835.e2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The t(11;22)(q24;q12) translocation is present in up to 95% of Ewing tumor patients and results in the formation of an EWS-FLI-1 fusion gene that encodes a chimeric transcription factor. Many alternative forms of EWS-FLI-1 exist because of variations in the location of the EWS and FLI-1 genomic breakpoints. Previous reports have shown that the type I fusion is associated with a significantly better prognosis than the other fusion types. It has been suggested that the observed clinical discrepancies result from different transactivation potentials of the various EWS-FLI-1 fusion proteins. In an attempt to identify genes whose expression levels are differentially modulated by structurally different EWS-FLI-1 transcription factors, we have used microarray technology to interrogate 19,000 sequence genes to compare gene expression profile of type I or non-type I Ewing sarcoma cell lines. Data analysis showed few qualitative differences on gene expression-expression of only 41 genes (0.215% of possible sequences analyzed) differed significantly between Ewing tumor cell lines carrying EWS-FLI-1 fusion type 1 with respect to those with non-type 1 fusion.
引用
收藏
页码:537 / 542
页数:6
相关论文
共 31 条
[1]   Biology of EWS/ETS fusions in Ewing's family tumors [J].
Arvand, A ;
Denny, CT .
ONCOGENE, 2001, 20 (40) :5747-5754
[2]   Variability in gene expression patterns of Ewing tumor cell lines differing in EWS-FLI1 fusion type [J].
Aryee, DNT ;
Sommergruber, W ;
Muehlbacher, K ;
Dockhorn-Dworniczak, B ;
Zoubek, A ;
Kovar, H .
LABORATORY INVESTIGATION, 2000, 80 (12) :1833-1844
[3]  
Bartman AE, 1999, INT J CANCER, V80, P210
[4]   Ets and retroviruses - transduction and activation of members of the Ets oncogene family in viral oncogenesis [J].
Blair, DG ;
Athanasiou, M .
ONCOGENE, 2000, 19 (55) :6472-6481
[5]   A CONSERVED BINDING MOTIF DEFINES NUMEROUS CANDIDATE TARGET PROTEINS FOR BOTH CDC42 AND RAC GTPASES [J].
BURBELO, PD ;
DRECHSEL, D ;
HALL, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (49) :29071-29074
[6]   Ewing family tumors: Potential prognostic value of reverse transcriptase polymerase chain reaction detection of minimal residual disease in peripheral blood samples [J].
de Alava, E ;
Lozano, MD ;
Patino, A ;
Sierrasesumaga, L ;
Pardo-Mindan, FJ .
DIAGNOSTIC MOLECULAR PATHOLOGY, 1998, 7 (03) :152-157
[7]   THE EWING FAMILY OF TUMORS - A SUBGROUP OF SMALL-ROUND-CELL TUMORS DEFINED BY SPECIFIC CHIMERIC TRANSCRIPTS [J].
DELATTRE, O ;
ZUCMAN, J ;
MELOT, T ;
GARAU, XS ;
ZUCKER, JM ;
LENOIR, GM ;
AMBROS, PF ;
SHEER, D ;
TURCCAREL, C ;
TRICHE, TJ ;
AURIAS, A ;
THOMAS, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (05) :294-299
[8]   GENE FUSION WITH AN ETS DNA-BINDING DOMAIN CAUSED BY CHROMOSOME-TRANSLOCATION IN HUMAN TUMORS [J].
DELATTRE, O ;
ZUCMAN, J ;
PLOUGASTEL, B ;
DESMAZE, C ;
MELOT, T ;
PETER, M ;
KOVAR, H ;
JOUBERT, I ;
DEJONG, P ;
ROULEAU, G ;
AURIAS, A ;
THOMAS, G .
NATURE, 1992, 359 (6391) :162-165
[9]   The prooncoprotein EWS binds calmodulin and is phosphorylated by protein kinase C through an IQ domain [J].
Deloulme, JC ;
Prichard, L ;
Delattre, O ;
Storm, DR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (43) :27369-27377
[10]  
Im YH, 2000, CANCER RES, V60, P1536