Co-amplification and overexpression of CDK4, SAS and MDM2 occurs frequently in human parosteal osteosarcomas

被引:127
作者
Wunder, JS
Eppert, K
Burrow, SR
Gogkoz, N
Bell, RS
Andrulis, IL
机构
[1] Univ Toronto, Dept Mol & Med Genet, Toronto, ON, Canada
[2] Univ Toronto, Lab Med & Pathobiol, Toronto, ON, Canada
[3] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[4] Mt Sinai Hosp, Univ Musculoskeletal Oncol Unit, Toronto, ON M5G 1X5, Canada
关键词
gene amplification; CDK4; SAS; osteosarcoma;
D O I
10.1038/sj.onc.1202346
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Amplification of genes in the 12q13-15 region occurs frequently in several malignancies including osteosarcoma. The products of these amplified genes are thought to provide cancer cells with a selective growth advantage; however, the specific gene(s) driving this amplicon is unknown. We have previously shown that the SAS gene is amplified in most parosteal osteosarcomas. In this study we analysed additional putative growth regulatory genes in this chromosomal region in 24 primary osteosarcoma specimens. CDK4 and SAS were coamplified in 6/6 parosteal tumors, and MDM2 was also amplified in 4/5 parosteal cases, In comparison, amplification occurred in only 2/16 classical intramedullary osteosarcomas and involved the SAS gene. Each amplified gene had a correspondingly elevated mRNA level. Four high grade intramedullary tumors had elevated mRNA expression of SAS, but did not exhibit gene amplification, Gene amplification/overexpression was not associated with metastatic disease and did not change markedly with tumor progression, as evidenced by analysis of sequential tumor specimens from eight patients. Three other genes in the 12q13-15 region (CDK2, WNT1 and WNT10b) were not amplified in any of the tumors. The different patterns of gene amplification and overexpression of CDK4, SAS and MDM2 in parosteal and intramedullary osteosarcomas may help explain the disparity in the biological behaviour of these two types of osteosarcoma.
引用
收藏
页码:783 / 788
页数:6
相关论文
共 71 条
[41]  
Mousses S, 1996, MODERN PATHOL, V9, P1
[42]   MDM2 GENE AMPLIFICATION IN BONE AND SOFT-TISSUE TUMORS - ASSOCIATION WITH TUMOR PROGRESSION IN DIFFERENTIATED ADIPOSE-TISSUE TUMORS [J].
NAKAYAMA, T ;
TOGUCHIDA, J ;
WADAYAMA, BI ;
KANOE, H ;
KOTOURA, Y ;
SASAKI, MS .
INTERNATIONAL JOURNAL OF CANCER, 1995, 64 (05) :342-346
[43]   CHARACTERIZATION OF THE 12Q13-15 AMPLICON IN SOFT-TISSUE TUMORS [J].
NILBERT, M ;
RYDHOLM, A ;
MITELMAN, F ;
MELTZER, PS ;
MANDAHL, N .
CANCER GENETICS AND CYTOGENETICS, 1995, 83 (01) :32-36
[44]   SAS is amplified predominantly in surface osteosarcoma [J].
NobleTopham, SE ;
Burrow, SR ;
Eppert, K ;
Kandel, RA ;
Meltzer, PS ;
Bell, RS ;
Andrulis, IL .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1996, 14 (05) :700-705
[45]   QUANTITATIVE-ANALYSIS OF MDR1 (MULTIDRUG RESISTANCE) GENE-EXPRESSION IN HUMAN TUMORS BY POLYMERASE CHAIN-REACTION [J].
NOONAN, KE ;
BECK, C ;
HOLZMAYER, TA ;
CHIN, JE ;
WUNDER, JS ;
ANDRULIS, IL ;
GAZDAR, AF ;
WILLMAN, CL ;
GRIFFITH, B ;
VONHOFF, DD ;
RONINSON, IB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (18) :7160-7164
[46]   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
[47]   SUPERNUMERARY RING CHROMOSOMES IN 5 BONE AND SOFT-TISSUE TUMORS OF LOW OR BORDERLINE MALIGNANCY [J].
ORNDAL, C ;
MANDAHL, N ;
RYDHOLM, A ;
WILLEN, H ;
BROSJO, O ;
HEIM, S ;
MITELMAN, F .
CANCER GENETICS AND CYTOGENETICS, 1992, 60 (02) :170-175
[48]  
RAYMOND AK, 1991, CLIN ORTHOP RELAT R, P140
[49]  
Reifenberger G, 1996, CANCER RES, V56, P5141
[50]  
REIFENBERGER G, 1994, CANCER RES, V54, P4299