COMPLEX COMPOSITION AND COAMPLIFICATION OF SAS AND MDM2 IN RING AND GIANT ROD MARKER CHROMOSOMES IN WELL-DIFFERENTIATED LIPOSARCOMA

被引:170
作者
PEDEUTOUR, F
SUIJKERBUIJK, RF
FORUS, A
VANGAAL, J
VANDEKLUNDERT, W
COINDRE, JM
NICOLO, G
COLLIN, F
VANHAELST, U
HUFFERMANN, K
TURCCAREL, C
机构
[1] LAB GENET MOLEC CANC HUMAINS,CNRS,URA 1462,F-06107 NICE 02,FRANCE
[2] CTR GEORGES FRANCOIS LEDERC,ANAT PATHOL LAB,DIJON,FRANCE
[3] FDN BERGONIE,ANAT PATHOL LAB,BORDEAUX,FRANCE
[4] UNIV NIJMEGEN HOSP,DEPT HUMAN GENET,6500 HB NIJMEGEN,NETHERLANDS
[5] UNIV NIJMEGEN HOSP,DEPT PATHOL,NIJMEGEN,NETHERLANDS
[6] NORWEGIAN RADIUM HOSP,DEPT TUMOR BIOL,OSLO,NORWAY
[7] IST NAZL RIC CANC,CITOISTOL PATOL LAB,I-16132 GENOA,ITALY
关键词
D O I
10.1002/gcc.2870100203
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Extra abnormal chromosomes (rings and giant rods) containing chromosome 12 sequences are characteristic of well-differentiated liposarcoma (WDLPS). By whole chromosome painting we found in 6 WDLPS that minimally 5 chromosomes had contributed to the formation of the extra abnormal chromosomes. To the constant chromosome 12 contribution, sequences were variably added from chromosomes 1, 4, and 16. Material from chromosomes 1, 4, and 12 was identified by painting in interphase nuclear projections (''blebs'') and in micronuclei consistent with the concept that blebs are precursors to micronuclei. The complexity of the mechanisms generating the extra abnormal chromosomes in WDLPS was also attested to by the diversity and, in some cases, intricacy of the patterns of fluorescence. To begin to fathom the function of the extra abnormal chromosomes we examined the amplification of genes, including SAS, MDM2, and GADDI53/CHOP, known to be in the region 12q13-14. SAS and MDM2 demonstrated constant co-amplification. GADDI53/CHOP, which is critically rearranged in myxoid liposarcoma, was not amplified in WDLPS. (C) 1994 Wiley-Liss, Inc.
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页码:85 / 94
页数:10
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