Gene expression profiling of clear cell renal cell carcinoma: Gene identification and prognostic classification

被引:307
作者
Takahashi, M
Rhodes, DR
Furge, KA
Kanayamat, H
Kagawa, S
Haab, BB
Teh, BT
机构
[1] Van Andel Res Inst, Canc Genet Lab, Grand Rapids, MI 49503 USA
[2] Van Andel Res Inst, Lab DNA & Prot Microrray Technol, Grand Rapids, MI 49503 USA
[3] Van Andel Res Inst, Mol Oncol Lab, Grand Rapids, MI 49503 USA
[4] Univ Tokushima, Sch Med, Dept Urol, Tokushima 7708503, Japan
关键词
D O I
10.1073/pnas.171209998
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To better understand the molecular mechanisms that underlie the tumorigenesis and progression of clear cell renal cell carcinoma (ccRCC), we studied the gene expression profiles of 29 ccRCC tumors obtained from patients with diverse clinical outcomes by using 21,632 cDNA microarrays. We identified gene expression alterations that were both common to most of the ccRCC studied and unique to clinical subsets. There was a significant distinction in gene expression profile between patients with a relatively non-aggressive form of the disease [100% survival after 5 years with the majority (15/17 or 88%) having no clinical evidence of metastasis] versus patients with a relatively aggressive form of the disease (average survival time 25.4 months with a 0% 5-year survival rate). Approximately 40 genes most accurately make this distinction, some of which have previously been implicated in turnorigenesis and metastasis. To test the robustness and potential clinical usefulness of this molecular distinction, we simulated its use as a prognostic tool in the clinical setting. In 96% of the ccRCC cases tested, the prediction was compatible with the clinical outcome, exceeding the accuracy of prediction by staging. These results suggest that two molecularly distinct forms of ccRCC exist and that the integration of expression profile data with clinical parameters could serve to enhance the diagnosis and prognosis of ccRCC. Moreover, the identified genes provide insight into the molecular mechanisms of aggressive ccRCC and suggest intervention strategies.
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页码:9754 / 9759
页数:6
相关论文
共 32 条
[1]  
Ahonen M, 1998, CANCER RES, V58, P2310
[2]   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
[3]  
Bachman KE, 1999, CANCER RES, V59, P798
[4]   Molecular classification of cutaneous malignant melanoma by gene expression profiling [J].
Bittner, M ;
Meitzer, P ;
Chen, Y ;
Jiang, Y ;
Seftor, E ;
Hendrix, M ;
Radmacher, M ;
Simon, R ;
Yakhini, Z ;
Ben-Dor, A ;
Sampas, N ;
Dougherty, E ;
Wang, E ;
Marincola, F ;
Gooden, C ;
Lueders, J ;
Glatfelter, A ;
Pollock, P ;
Carpten, J ;
Gillanders, E ;
Leja, D ;
Dietrich, K ;
Beaudry, C ;
Berens, M ;
Alberts, D ;
Sondak, V ;
Hayward, N ;
Trent, J .
NATURE, 2000, 406 (6795) :536-540
[5]  
Edgren M, 1999, ANTICANCER RES, V19, P869
[6]   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
[7]  
Eisen MB, 1999, METHOD ENZYMOL, V303, P179
[8]   Transforming growth factor-beta type II receptor confers tumor suppressor activity in murine renal carcinoma (RENCA) cells [J].
Engel, JD ;
Kundu, SD ;
Yang, T ;
Yang, S ;
Goodwin, S ;
Janulis, L ;
Cho, JS ;
Chang, J ;
Kim, SJ ;
Lee, C .
UROLOGY, 1999, 54 (01) :164-170
[9]   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
[10]   Gene-expression profiles in hereditary breast cancer. [J].
Hedenfalk, I ;
Duggan, D ;
Chen, YD ;
Radmacher, M ;
Bittner, M ;
Simon, R ;
Meltzer, P ;
Gusterson, B ;
Esteller, M ;
Kallioniemi, OP ;
Wilfond, B ;
Borg, Å ;
Trent, J ;
Raffeld, M ;
Yakhini, Z ;
Ben-Dor, A ;
Dougherty, E ;
Kononen, J ;
Bubendorf, L ;
Fehrle, W ;
Pittaluga, S ;
Gruvberger, S ;
Loman, N ;
Johannsoson, O ;
Olsson, H ;
Sauter, G .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (08) :539-548