Discordant protein and mRNA expression in lung adenocarcinomas

被引:785
作者
Chen, GA
Gharib, TG
Huang, CC
Taylor, JMG
Misek, DE
Kardia, SLR
Giordano, TJ
Iannettoni, MD
Orringer, MB
Hanash, SM
Beer, DG
机构
[1] Univ Michigan, Sch Med, Dept Surg, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Biostat, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Dept Epidemiol, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Sch Med, Dept Pediat, Ann Arbor, MI 48109 USA
关键词
D O I
10.1074/mcp.M200008-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The relationship between gene expression measured at the mRNA level and the corresponding protein level is not well characterized in human cancer. In this study, we compared mRNA and protein expression for a cohort of genes in the same lung adenocarcinomas. The abundance of 165 protein spots representing 98 individual genes was analyzed in 76 lung adenocarcinomas and nine non-neoplastic lung tissues using two-dimensional polyacrylamide gel electrophoresis. Specific polypeptides were identified using matrix-assisted laser desorption/ ionization mass spectrometry. For the same 85 samples, mRNA levels were determined using oligonucleotide microarrays, allowing a comparative analysis of mRNA and protein expression among the 165 protein spots. Twenty-eight of the 165 protein spots (17%) or 21 of 98 genes (21.4%) had a statistically significant correlation between protein and mRNA expression (r > 0.2445; p < 0.05); however, among all 165 proteins the correlation coefficient values (r) ranged from -0.467 to 0.442. Correlation coefficient values were not related to protein abundance. Further, no significant correlation between mRNA and protein expression was found (r = -0.025) if the average levels of mRNA or protein among all samples were applied across the 165 protein spots (98 genes). The mRNA/ protein correlation coefficient also varied among proteins with multiple isoforms, indicating potentially separate isoform-specific mechanisms for the regulation of protein abundance. Among the 21 genes with a significant correlation between mRNA and protein, five genes differed significantly between stage I and stage III lung adenocarcinomas. Using a quantitative analysis of mRNA and protein expression within the same lung adenocarcinomas, we showed that only a subset of the proteins exhibited a significant correlation with mRNA abundance.
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页码:304 / 313
页数:10
相关论文
共 25 条
[1]   A comparison of selected mRNA and protein abundances in human liver [J].
Anderson, L ;
Seilhamer, J .
ELECTROPHORESIS, 1997, 18 (3-4) :533-537
[2]   Proteome and proteomics: New technologies, new concepts, and new words [J].
Anderson, NL ;
Anderson, NG .
ELECTROPHORESIS, 1998, 19 (11) :1853-1861
[3]   Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses [J].
Bhattacharjee, A ;
Richards, WG ;
Staunton, J ;
Li, C ;
Monti, S ;
Vasa, P ;
Ladd, C ;
Beheshti, J ;
Bueno, R ;
Gillette, M ;
Loda, M ;
Weber, G ;
Mark, EJ ;
Lander, ES ;
Wong, W ;
Johnson, BE ;
Golub, TR ;
Sugarbaker, DJ ;
Meyerson, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13790-13795
[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]   An immune response manifested by the common occurrence of annexins I and II autoantibodies and high circulating levels of IL-6 in lung cancer [J].
Brichory, FM ;
Misek, DE ;
Yim, AM ;
Krause, MC ;
Giordano, TJ ;
Beer, DG ;
Hanash, SM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (17) :9824-9829
[6]   Gene expression profiling:: monitoring transcription and translation products using DNA microarrays and proteomics [J].
Celis, JE ;
Kruhoffer, M ;
Gromova, I ;
Frederiksen, C ;
Ostergaard, M ;
Thykjaer, T ;
Gromov, P ;
Yu, JS ;
Pálsdóttir, H ;
Magnusson, N ;
Orntoft, TF .
FEBS LETTERS, 2000, 480 (01) :2-16
[7]   Accessing genetic information with high-density DNA arrays [J].
Chee, M ;
Yang, R ;
Hubbell, E ;
Berno, A ;
Huang, XC ;
Stern, D ;
Winkler, J ;
Lockhart, DJ ;
Morris, MS ;
Fodor, SPA .
SCIENCE, 1996, 274 (5287) :610-614
[8]   Bioinformatics beyond sequence: Mapping gene function in the embryo [J].
Davidson, D ;
Baldock, R .
NATURE REVIEWS GENETICS, 2001, 2 (06) :409-417
[9]   2D or not 2D [J].
Fey, SJ ;
Larsen, PM .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2001, 5 (01) :26-33
[10]  
Fung ET, 2000, CURR OPIN MOL THER, V2, P643