Microarray analysis of xenograft-derived cancer cell lines representing multiple experimental models of human prostate cancer

被引:22
作者
Glinsky, GV [1 ]
Krones-Herzig, A [1 ]
Glinskii, AB [1 ]
Gebauer, G [1 ]
机构
[1] Sidney Kimmel Canc Ctr, San Diego, CA 92121 USA
关键词
prostate cancer cell lines; cDNA microarray; gene expression; nude mouse model;
D O I
10.1002/mc.10139
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
Expression analysis of 7129 transcripts was carried out in five human prostate cancer cell lines derived from orthotopic xenografts after one to five passages in nude mice and primary cultures of human normal prostate epithelial (NPE) cells. These experiments identified a consensus class of 214 genes (43 up- and 171 downregulated transcripts), expression of which was altered at least twofold in the same direction in all the cell lines relative to NPE cells. To validate the relevance of altered expression behavior of these genes for human prostate cancer, their expression pattern was evaluated in multiple additional experimental and clinical settings. Expression of 170 of these 214 genes (79%) was altered in the same direction in vivo in experimental human prostate tumors in mice. Similarly, the expression of 151 of the 214 genes (71 %) was altered in the same direction in M 12 cells, a variant of an SV40 large T antigen transformed normal human prostate epithelial cell line selected for increased malignancy in vivo. In clinical samples of human prostate tumors, the changes in transcript expression levels of majority of these genes (85% of downregulated and 76% of upregulated transcripts) are consistent with alterations of their expression pattern in xenograft-derived cancer cell lines. These results imply that the expression pattern of a large class of genes is consistently altered in multiple experimental models and clinical samples of human prostate cancer and underscore the potential relevance of the xenograft models and cell lines derived from them for expression analysis studies relevant to human cancer. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:209 / 221
页数:13
相关论文
共 37 条
[1]  
An ZL, 1998, PROSTATE, V34, P169
[2]   TUMORIGENICITY OF SV40 T-ANTIGEN IMMORTALIZED HUMAN PROSTATE EPITHELIAL-CELLS - ASSOCIATION WITH DECREASED EPIDERMAL GROWTH-FACTOR RECEPTOR (EGFR) EXPRESSION [J].
BAE, VL ;
JACKSONCOOK, CK ;
BROTHMAN, AR ;
MAYGARDEN, SJ ;
WARE, JL .
INTERNATIONAL JOURNAL OF CANCER, 1994, 58 (05) :721-729
[3]  
Bae VL, 1998, PROSTATE, V34, P275, DOI 10.1002/(SICI)1097-0045(19980301)34:4<275::AID-PROS5>3.0.CO
[4]  
2-G
[5]   Transcriptional activation by p53 of the human type IV collagenase (gelatinase A or matrix metalloproteinase 2) promoter [J].
Bian, JH ;
Sun, Y .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (11) :6330-6338
[6]   p53 regulates caveolin gene transcription, cell cholesterol, and growth by a novel mechanism [J].
Bist, A ;
Fielding, CJ ;
Fielding, PE .
BIOCHEMISTRY, 2000, 39 (08) :1966-1972
[7]   CONTROL OF ANGIOGENESIS IN FIBROBLASTS BY P53 REGULATION OF THROMBOSPONDIN-1 [J].
DAMERON, KM ;
VOLPERT, OV ;
TAINSKY, MA ;
BOUCK, N .
SCIENCE, 1994, 265 (5178) :1582-1584
[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]   Thrombospondin-1, vascular endothelial growth factor and fibroblast growth factor-2 are key functional regulators of angiogenesis in the prostate [J].
Doll, JA ;
Reiher, FK ;
Crawford, SE ;
Pins, MR ;
Campbell, SC ;
Bouck, NP .
PROSTATE, 2001, 49 (04) :293-305
[10]   MOLECULAR-CLONING AND TISSUE EXPRESSION OF FAT, THE HUMAN HOMOLOG OF THE DROSOPHILA FAT GENE THAT IS LOCATED ON CHROMOSOME 4Q34-Q35 AND ENCODES A PUTATIVE ADHESION MOLECULE [J].
DUNNE, J ;
HANBY, AM ;
POULSOM, R ;
JONES, TA ;
SHEER, D ;
CHIN, WG ;
DA, SM ;
ZHAO, Q ;
BEVERLEY, PCL ;
OWEN, MJ .
GENOMICS, 1995, 30 (02) :207-223