Expression profile of genes from 12p in testicular germ cell tumors of adolescents and adults associated with i(12p) and amplification at 12p11.2-p12.1

被引:130
作者
Rodriguez, S
Jafer, O
Goker, H
Summersgill, BM
Zafarana, G
Gillis, AJM
van Gurp, RJHLM
Oosterhuis, JW
Lu, YJ
Huddart, R
Cooper, CS
Clark, J
Looijenga, LHJ
Shipley, JM
机构
[1] Inst Canc Res, Male Urol Canc Res Ctr, Sutton SM2 5NG, Surrey, England
[2] Erasmus MC Univ, Med Ctr, Dr Daniel Den Hoed Canc Ctr, Josephine Nefkens Inst,Pathol Lab Expt Pathooncol, NL-3000 DR Rotterdam, Netherlands
[3] Inst Canc Res, Sect Paediat Oncol, Sutton SM2 5NG, Surrey, England
[4] Royal Marsden Natl Hlth Serv Trust, Acad Dept Urol, Surrey, England
[5] Inst Canc Res, Sect Mol Carcinogenesis, Sutton SM2 5NG, Surrey, England
关键词
testicular germ cell tumors of adolescents and adults; isochromosome; 12p; amplification; microarray expression profiling; comparative expressed sequence hybridization; candidate genes;
D O I
10.1038/sj.onc.1206302
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
Gain of 12p material is invariably associated with testicular germ cell tumors (TGCTs) of adolescents and adults, most usually as an isochromosome 12p. We analyzed TGCTs with i(12p) using a global approach to expression profiling targeting chromosomes (comparative expressed sequence hybridization, CESH). This indicated overexpression of genes from 12p11.2-p12.1 relative to testis tissue and fibroblasts. The nonseminoma subtype showed higher levels of expression than seminomas. Notably, 12p11.2-p12.1 is amplified in about 10% of TGCTs and CESH analysis of such amplicon cases showed high levels of overexpression from this region. Microarray analysis, including cDNA clones representing most UniGene clusters from 12p11.2-p12.1, was applied to DNA and RNA from 5 TGCTs with amplification of 12p11.2-p12.1 and seven TGCTs with gain of the entire short arm of chromosome 12. Expression profiles were consistent with the CESH data and overexpression of EST595078, MRPS35 and LDHB at 12p11.2-p12.1 was detected in most TGCTs. High-level overexpression of BCAT1 was specific to nonseminomas and overexpression of genes such as CMAS, EKI1, KRAS2, SURB7 and various ESTs correlated with their amplification. Genes such as CCND2, GLU3, LRP6 and HPH1 at 12p13 were also overexpressed. The overexpressed sequences identified, particularly those in the region amplified, represent candidate genes for involvement in TGCT development.
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页码:1880 / 1891
页数:12
相关论文
共 35 条
[1]  
ATKIN NB, 1982, LANCET, V2, P1349
[2]  
BALDINI A, 1990, AM J HUM GENET, V46, P784
[3]   Involvement of Myc targets in c-myc and N-myc induced human tumors [J].
Ben-Yosef, T ;
Yanuka, O ;
Halle, D ;
Benvenisty, N .
ONCOGENE, 1998, 17 (02) :165-171
[4]   AN EMBRYONICALLY EXPRESSED GENE IS A TARGET FOR C-MYC REGULATION VIA THE C-MYC-BINDING SEQUENCE [J].
BENVENISTY, N ;
LEDER, A ;
KUO, A ;
LEDER, P .
GENES & DEVELOPMENT, 1992, 6 (12B) :2513-2523
[5]   Testicular germ-cell cancer [J].
Bosl, GJ ;
Motzer, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (04) :242-253
[6]  
Bourdon V, 2002, CANCER RES, V62, P6218
[7]   Identification of amplified and expressed genes in breast cancer by comparative hybridization onto microarrays of randomly selected cDNA clones [J].
Clark, J ;
Edwards, S ;
John, M ;
Flohr, P ;
Gordon, T ;
Maillard, K ;
Giddings, I ;
Brown, C ;
Bagherzadeh, A ;
Campbell, C ;
Shipley, J ;
Wooster, R ;
Cooper, CS .
GENES CHROMOSOMES & CANCER, 2002, 34 (01) :104-114
[8]   ROBUST LOCALLY WEIGHTED REGRESSION AND SMOOTHING SCATTERPLOTS [J].
CLEVELAND, WS .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1979, 74 (368) :829-836
[9]   C-erbB-2 in breast cancer: Development of a clinically useful marker [J].
Hayes, DF ;
Thor, AD .
SEMINARS IN ONCOLOGY, 2002, 29 (03) :231-245
[10]   Cell death by pyruvate deficiency in proliferative cultured calvarial osteoblasts [J].
Hinoi, E ;
Fujimori, S ;
Takemori, A ;
Yoneda, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 294 (05) :1177-1183