Identification of CD70 as a diagnostic biomarker for clear cell renal cell carcinoma by gene expression profiling, real-time RT-PCR and immunohistochemistry

被引:64
作者
Diegmann, J
Junker, K
Gerstmayer, B
Bosio, A
Hindermann, W
Rosenhahn, J
von Eggeling, F [1 ]
机构
[1] Univ Jena, Inst Human Genet & Anthropol, Core Unit Chip Applicat, D-07740 Jena, Germany
[2] Univ Jena, Dept Urol, D-07743 Jena, Germany
[3] Memorec Biotech GmbH, Med Mol Res Cologne, D-50829 Cologne, Germany
[4] Univ Jena, Inst Pathol, D-07743 Jena, Germany
关键词
cDNA-arrays; LightCycler; kidney; microarray; marker gene;
D O I
10.1016/j.ejca.2005.05.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The underlying molecular mechanisms or renal cell carcinoma (RCC) are poorly understood and more reliable markers for early diagnosis are needed. Hence, alternative strategies for biomarker discovery with appropriate validation technologies have to be performed. To elucidate genesis and progression of RCC we used high parallel chip based gene expression profiling comparing normal and tumour tissues. We compared corresponding control and tumour tissue samples from 10 patients with clear cell RCC. We isolated RNA from histologically well characterised tissue sections and performed reverse transcription, labelling and linear RNA amplification. Samples were hybridised on microarrays containing 642 human cDNAs. Of the 352 differentially expressed genes found, CD70 and FRA2 were selected for further evaluation by real-time RT-PCR. The analysis all showed a high potential to discriminate between normal and tumour tissue. Moreover, increased CD70 mRNA expression in tumour cells could be correlated to its expression at the protein level. Immunohistochemistry (IHC) showed very strong expression of CD70 in all tumour samples but no expression in adjacent normal kidney tissue. With our combined approach we were able to identify CD70 as a new marker for RCC, which may be useful in the future for improved immunohistochemical diagnosis. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1794 / 1801
页数:8
相关论文
共 24 条
[1]  
[Anonymous], 2004, PATHOLOGY GENETICS T
[2]   Identification and classification of differentially expressed genes in renal cell carcinoma by expression profiling on a global human 31,500-element cDNA array [J].
Boer, JM ;
Huber, WK ;
Sültmann, H ;
Wilmer, F ;
von Heydebreck, A ;
Haas, S ;
Korn, B ;
Gunawan, B ;
Vente, A ;
Füzesi, L ;
Vingron, M ;
Poustka, A .
GENOME RESEARCH, 2001, 11 (11) :1861-1870
[3]   Minimum information about a microarray experiment (MIAME) - toward standards for microarray data [J].
Brazma, A ;
Hingamp, P ;
Quackenbush, J ;
Sherlock, G ;
Spellman, P ;
Stoeckert, C ;
Aach, J ;
Ansorge, W ;
Ball, CA ;
Causton, HC ;
Gaasterland, T ;
Glenisson, P ;
Holstege, FCP ;
Kim, IF ;
Markowitz, V ;
Matese, JC ;
Parkinson, H ;
Robinson, A ;
Sarkans, U ;
Schulze-Kremer, S ;
Stewart, J ;
Taylor, R ;
Vilo, J ;
Vingron, M .
NATURE GENETICS, 2001, 29 (04) :365-371
[4]   Prognostic value of carbonic anhydrase IX and Ki67 as predictors of survival for renal clear cell carcinoma [J].
Bui, MHT ;
Visapaa, H ;
Seligson, D ;
Kim, H ;
Han, KR ;
Huang, Y ;
Horvath, S ;
Stanbridge, EJ ;
Palotie, A ;
Figlin, RA ;
Belldegrun, AS .
JOURNAL OF UROLOGY, 2004, 171 (06) :2461-2466
[5]  
Bui MHT, 2003, CLIN CANCER RES, V9, P802
[6]   The expression of CD70 and CD80 by gene-modified tumor cells induces an antitumor response depending on the MHC status [J].
Douin-Echinard, V ;
Bornes, S ;
Rochaix, P ;
Tilkin, AF ;
Peron, JM ;
Bonnet, J ;
Favre, G ;
Couderc, B .
CANCER GENE THERAPY, 2000, 7 (12) :1543-1556
[7]  
Eberwine J, 1996, BIOTECHNIQUES, V20, P584
[8]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[9]  
Gerritsen ME, 2002, EXP NEPHROL, V10, P114
[10]   Molecular classification of cancer: Class discovery and class prediction by gene expression monitoring [J].
Golub, TR ;
Slonim, DK ;
Tamayo, P ;
Huard, C ;
Gaasenbeek, M ;
Mesirov, JP ;
Coller, H ;
Loh, ML ;
Downing, JR ;
Caligiuri, MA ;
Bloomfield, CD ;
Lander, ES .
SCIENCE, 1999, 286 (5439) :531-537