Analysis of gene-expression profiles in testicular seminomas using a genome-wide cDNA microarray

被引:5
作者
Okada, K
Katagiri, T
Tsunoda, T
Mizutani, Y
Suzuki, Y
Kamada, M
Fujioka, T
Shuin, T
Miki, T
Nakamura, Y
机构
[1] Univ Tokyo, Inst Med Sci, Mol Med Lab, Ctr Human Genome,Minato Ku, Tokyo 1088639, Japan
[2] RIKEN, Inst Phys & Chem Res, SNP Res Ctr, Lab Med Informat,Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[3] Kyoto Prefectural Univ Med, Dept Urol, Kamigyo Ku, Kyoto 6028566, Japan
[4] Iwate Med Univ, Sch Med, Dept Urol, Morioka, Iwate 0208505, Japan
[5] Kochi Med Sch, Dept Urol, Kochi 7838505, Japan
关键词
testicular germ cell tumor; seminoma; cDNA microarray;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To identify new diagnostic markers for testicular germ cell tumors (TGCTs), including seminomas, as well as potential targets of new drugs for treating the disease, we compared gene-expression profiles of cancer cells from 13 seminomas with normal human testis using laser-capture microdissection and a cDNA microarray representing 23,040 genes. We identified 347 genes that were commonly up-regulated in seminoma cells. The functions of 227 were known to some extent; the remaining 120 included 55 ESTs. On the list were cyclin D2 (CCND2), prostate cancer over-expressed gene 1 (POV1), and junction plakoglobin (JUP), all of which were already known to be over-expressed in seminomas. On the other hand, our protocol selected 593 genes as being commonly down-regulated in seminoma cells. That list included 340 functionally characterized genes; the other 253 included 131 ESTs. To confirm the expression data, we performed semi-quantitative RT-PCR experiments with nine highly up-regulated genes, and the results supported those of our microarray analysis. The information provided here should prove useful for identifying genes whose products might serve as molecular targets for treatment of TGCTs.
引用
收藏
页码:1615 / 1635
页数:21
相关论文
共 39 条
[1]   Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling [J].
Alizadeh, AA ;
Eisen, MB ;
Davis, RE ;
Ma, C ;
Lossos, IS ;
Rosenwald, A ;
Boldrick, JG ;
Sabet, H ;
Tran, T ;
Yu, X ;
Powell, JI ;
Yang, LM ;
Marti, GE ;
Moore, T ;
Hudson, J ;
Lu, LS ;
Lewis, DB ;
Tibshirani, R ;
Sherlock, G ;
Chan, WC ;
Greiner, TC ;
Weisenburger, DD ;
Armitage, JO ;
Warnke, R ;
Levy, R ;
Wilson, W ;
Grever, MR ;
Byrd, JC ;
Botstein, D ;
Brown, PO ;
Staudt, LM .
NATURE, 2000, 403 (6769) :503-511
[2]   The human Pim-2 proto-oncogene and its testicular expression [J].
Baytel, D ;
Shalom, S ;
Madgar, I ;
Weissenberg, R ;
Don, J .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1998, 1442 (2-3) :274-285
[3]   Increase in testicular cancer incidence in six European countries: A birth cohort phenomenon [J].
Bergstrom, R ;
Adami, HO ;
Mohner, M ;
Zatonski, W ;
Storm, H ;
Ekbom, A ;
Tretli, S ;
Teppo, L ;
Akre, O ;
Hakulinen, T .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (11) :727-733
[4]   Regulatory and signaling properties of the Vav family [J].
Bustelo, XR .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (05) :1461-1477
[5]  
Chaganti RSK, 2000, CANCER RES, V60, P1475
[6]   Identification of a novel transcript up-regulated in a clinically aggressive prostate carcinoma [J].
Chuaqui, RF ;
Englert, CR ;
Strup, SE ;
Vocke, CD ;
Zhuang, ZP ;
Duray, PH ;
Bostwick, DG ;
Linehan, WM ;
Liotta, LA ;
EmmertBuck, MR .
UROLOGY, 1997, 50 (02) :302-307
[7]  
Davies R, 1999, CANCER RES, V59, p1747S
[8]   Delineation of prognostic biomarkers in prostate cancer [J].
Dhanasekaran, SM ;
Barrette, TR ;
Ghosh, D ;
Shah, R ;
Varambally, S ;
Kurachi, K ;
Pienta, KJ ;
Rubin, MA ;
Chinnaiyan, AM .
NATURE, 2001, 412 (6849) :822-826
[9]  
Dieckmann KP, 1997, CANCER, V80, P1954, DOI 10.1002/(SICI)1097-0142(19971115)80:10<1954::AID-CNCR12>3.3.CO
[10]  
2-6