Microarray based diagnosis profits from better documentation of gene expression signatures

被引:20
作者
Kostka, Dennis [1 ]
Spang, Rainer [2 ]
机构
[1] Max Planck Inst Mol Genet, Dept Computat Mol Biol, Berlin, Germany
[2] Univ Regensburg, Computat Diagnost Grp, Inst Funct Gen, Regensburg, Germany
关键词
D O I
10.1371/journal.pcbi.0040022
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microarray gene expression signatures hold great promise to improve diagnosis and prognosis of disease. However, current documentation standards of such signatures do not allow for an unambiguous application to study-external patients. This hinders independent evaluation, effectively delaying the use of signatures in clinical practice. Data from eight publicly available clinical microarray studies were analyzed and the consistency of study-internal with study-external diagnoses was evaluated. Study-external classifications were based on documented information only. Documenting a signature is conceptually different from reporting a list of genes. We show that even the exact quantitative specification of a classification rule alone does not define a signature unambiguously. We found that discrepancy between study-internal and study-external diagnoses can be as frequent as 30% (worst case) and 18% (median). By using the proposed documentation by value strategy, which documents quantitative preprocessing information, the median discrepancy was reduced to 1%. The process of evaluating microarray gene expression diagnostic signatures and bringing them to clinical practice can be substantially improved and made more reliable by better documentation of the signatures.
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页数:6
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共 29 条
  • [1] Affymetrix, 2002, STAT ALG DESCR DOC
  • [2] Gene-expression profiles predict survival of patients with lung adenocarcinoma
    Beer, DG
    Kardia, SLR
    Huang, CC
    Giordano, TJ
    Levin, AM
    Misek, DE
    Lin, L
    Chen, GA
    Gharib, TG
    Thomas, DG
    Lizyness, ML
    Kuick, R
    Hayasaka, S
    Taylor, JMG
    Iannettoni, MD
    Orringer, MB
    Hanash, S
    [J]. NATURE MEDICINE, 2002, 8 (08) : 816 - 824
  • [3] Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses
    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
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) : 13790 - 13795
  • [4] Biganzoli E, 2005, LANCET, V365, P1683, DOI 10.1016/S0140-6736(05)66537-3
  • [5] Oncogenic pathway signatures in human cancers as a guide to targeted therapies
    Bild, AH
    Yao, G
    Chang, JT
    Wang, QL
    Potti, A
    Chasse, D
    Joshi, MB
    Harpole, D
    Lancaster, JM
    Berchuck, A
    Olson, JA
    Marks, JR
    Dressman, HK
    West, M
    Nevins, JR
    [J]. NATURE, 2006, 439 (7074) : 353 - 357
  • [6] A comparison of normalization methods for high density oligonucleotide array data based on variance and bias
    Bolstad, BM
    Irizarry, RA
    Åstrand, M
    Speed, TP
    [J]. BIOINFORMATICS, 2003, 19 (02) : 185 - 193
  • [7] A COEFFICIENT OF AGREEMENT FOR NOMINAL SCALES
    COHEN, J
    [J]. EDUCATIONAL AND PSYCHOLOGICAL MEASUREMENT, 1960, 20 (01) : 37 - 46
  • [8] A benchmark for affymetrix GeneChip expression measures
    Cope, LM
    Irizarry, RA
    Jaffee, HA
    Wu, ZJ
    Speed, TP
    [J]. BIOINFORMATICS, 2004, 20 (03) : 323 - 331
  • [9] Hastie T, 2004, J MACH LEARN RES, V5, P1391
  • [10] Gene expression predictors of breast cancer outcomes
    Huang, E
    Cheng, SH
    Dressman, H
    Pittman, J
    Tsou, MH
    Horng, CF
    Bild, A
    Iversen, ES
    Liao, M
    Chen, CM
    West, M
    Nevins, JR
    Huang, AT
    [J]. LANCET, 2003, 361 (9369) : 1590 - 1596