MDM2 GENE AMPLIFICATION IN BONE AND SOFT-TISSUE TUMORS - ASSOCIATION WITH TUMOR PROGRESSION IN DIFFERENTIATED ADIPOSE-TISSUE TUMORS

被引:112
作者
NAKAYAMA, T
TOGUCHIDA, J
WADAYAMA, BI
KANOE, H
KOTOURA, Y
SASAKI, MS
机构
[1] KYOTO UNIV,CTR RADIAT BIOL,SAKYO KU,KYOTO 606,JAPAN
[2] KYOTO UNIV,BIOMED ENGN RES CTR,SAKYO KU,KYOTO 606,JAPAN
关键词
D O I
10.1002/ijc.2910640511
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have studied 107 bone and soft-tissue sarcomas and 8 lipomas for amplification of the MDM2 gene. This gene was amplified in 3 out of 67 osteosarcomas, 3 out of 20 malignant fibrous histiocytomas, 4 out of 20 liposarcomas, and 4 out of 8 lipomas. The amplification was associated with overexpression of mRNA. In osteosarcomas, contrary to previous findings, all amplifications were observed in primary lesions. In liposarcomas, the amplification was seen exclusively in well-differentiated tumors with high frequency (4/5) but not in other subtypes (0/15). In addition, MDM2 amplification was also frequently found in deep-seated intra- or intermuscular lipomas (4/5). Hence, it is suggested that MDM2 amplification plays a significant role in the development of differentiated adipose-tissue tumors. Three well-differentiated liposarcomas with MDM2 amplification coexisted with high-grade dedifferentiated sarcomas, in which MDM2 amplification was also observed. Interestingly, in 2 of these cases, the grades of amplification correlated with the histological grades, indicating an important role of MDM2 overexpression in tumor progression. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:342 / 346
页数:5
相关论文
共 20 条
[11]   THE MDM-2 ONCOGENE PRODUCT FORMS A COMPLEX WITH THE P53 PROTEIN AND INHIBITS P53-MEDIATED TRANSACTIVATION [J].
MOMAND, J ;
ZAMBETTI, GP ;
OLSON, DC ;
GEORGE, D ;
LEVINE, AJ .
CELL, 1992, 69 (07) :1237-1245
[12]   MDM2 GENE AMPLIFICATION CORRELATES WITH RING CHROMOSOMES IN SOFT-TISSUE TUMORS [J].
NILBERT, M ;
RYDHOLM, A ;
WILLEN, H ;
MITELMAN, F ;
MANDAHL, N .
GENES CHROMOSOMES & CANCER, 1994, 9 (04) :261-265
[13]   AMPLIFICATION OF A GENE ENCODING A P53-ASSOCIATED PROTEIN IN HUMAN SARCOMAS [J].
OLINER, JD ;
KINZLER, KW ;
MELTZER, PS ;
GEORGE, DL ;
VOGELSTEIN, B .
NATURE, 1992, 358 (6381) :80-83
[14]   COMPLEX COMPOSITION AND COAMPLIFICATION OF SAS AND MDM2 IN RING AND GIANT ROD MARKER CHROMOSOMES IN WELL-DIFFERENTIATED LIPOSARCOMA [J].
PEDEUTOUR, F ;
SUIJKERBUIJK, RF ;
FORUS, A ;
VANGAAL, J ;
VANDEKLUNDERT, W ;
COINDRE, JM ;
NICOLO, G ;
COLLIN, F ;
VANHAELST, U ;
HUFFERMANN, K ;
TURCCAREL, C .
GENES CHROMOSOMES & CANCER, 1994, 10 (02) :85-94
[15]   FUSION OF THE DOMINANT-NEGATIVE TRANSCRIPTION REGULATOR CHOP WITH A NOVEL GENE FUS BY TRANSLOCATION T(12-16) IN MALIGNANT LIPOSARCOMA [J].
RABBITTS, TH ;
FORSTER, A ;
LARSON, R ;
NATHAN, P .
NATURE GENETICS, 1993, 4 (02) :175-180
[16]  
REIFENBERGER G, 1993, CANCER RES, V53, P2736
[17]  
Sambrook J., 1989, MOL CLONING LAB MANU
[18]  
TOGUCHIDA J, 1992, CANCER RES, V52, P6194
[19]   CYTOGENETIC STUDIES OF ADIPOSE-TISSUE TUMORS .2. RECURRENT RECIPROCAL TRANSLOCATION T(12-16)(Q13-P11) IN MYXOID LIPOSARCOMAS [J].
TURCCAREL, C ;
LIMON, J ;
DALCIN, P ;
RAO, U ;
KARAKOUSIS, C ;
SANDBERG, AA .
CANCER GENETICS AND CYTOGENETICS, 1986, 23 (04) :291-299
[20]   P53 EXPRESSION AND ITS RELATIONSHIP TO DNA ALTERATIONS IN BONE AND SOFT-TISSUE SARCOMAS [J].
WADAYAMA, B ;
TOGUCHIDA, J ;
YAMAGUCHI, T ;
SASAKI, MS ;
KOTOURA, Y ;
YAMAMURO, T .
BRITISH JOURNAL OF CANCER, 1993, 68 (06) :1134-1139