Gene expression profiling of cancer by use of DNA arrays: how far from the clinic?

被引:59
作者
Bertucci, F
Houlgatte, R
Nguyen, C
Viens, P
Jordan, BR
Birnbaum, D
机构
[1] IFR57, INSERM, U119, Oncol Mol Lab,IPC,TAGC, F-13009 Marseille, France
[2] IFR57, CIML Luminy, TAGC, Marseille, France
[3] Univ Aix Marseille 2, Marseille, France
[4] Marseille Genopole, Marseille, France
关键词
D O I
10.1016/S1470-2045(01)00557-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
DNA arrays allow the simultaneous analysis of expression levels for thousands of genes in normal and pathological tissues and hold great promise in molecular medicine, notably in cancer research. The great biological and clinical diversity present in human tumours is poorly characterised by the current classification systems. DNA arrays can provide a better understanding of oncogenesis, leading to improvements in cancer management. First, the identification of new target genes and pathways will allow the development of specific molecular-based anticancer drugs. Secondly, expression profiles will permit tumour classification in more homogeneous diagnostic and prognostic groups, as well as the identification of new clinically and biologically relevant tumour subclasses. Here, we review the technology and present some cancer studies with promising results. Finally, we discuss some of the issues that must be resolved in the near future, so that DNA arrays can fulfil the aims mentioned above.
引用
收藏
页码:674 / 682
页数:9
相关论文
共 69 条
  • [41] DIFFERENTIAL GENE-EXPRESSION IN THE MURINE THYMUS ASSAYED BY QUANTITATIVE HYBRIDIZATION OF ARRAYED CDNA CLONES
    NGUYEN, C
    ROCHA, D
    GRANJEAUD, S
    BALDIT, M
    BERNARD, K
    NAQUET, P
    JORDAN, BR
    [J]. GENOMICS, 1995, 29 (01) : 207 - 216
  • [42] Status of bcr-abl tyrosine kinase inhibitors in chronic myelogenous leukemia
    O'Dwyer, ME
    Druker, BJ
    [J]. CURRENT OPINION IN ONCOLOGY, 2000, 12 (06) : 594 - 597
  • [43] Ono K, 2000, CANCER RES, V60, P5007
  • [44] PARKIN DM, 1990, INT J CANCER, V80, P827
  • [45] Inhibitory effects of combinations of HER-2/neu antibody and chemotherapeutic agents used for treatment of human breast cancers
    Pegram, M
    Hsu, S
    Lewis, G
    Pietras, R
    Beryt, M
    Sliwkowski, M
    Coombs, D
    Baly, D
    Kabbinavar, F
    Slamon, D
    [J]. ONCOGENE, 1999, 18 (13) : 2241 - 2251
  • [46] Keeping genome databases clean and up to date
    Pennisi, E
    [J]. SCIENCE, 1999, 286 (5439) : 447 - 450
  • [47] Distinctive gene expression patterns in human mammary epithelial cells and breast cancers
    Perou, CM
    Jeffrey, SS
    Van de Rijn, M
    Rees, CA
    Eisen, MB
    Ross, DT
    Pergamenschikov, A
    Williams, CF
    Zhu, SX
    Lee, JCF
    Lashkari, D
    Shalon, D
    Brown, PO
    Botstein, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (16) : 9212 - 9217
  • [48] Molecular portraits of human breast tumours
    Perou, CM
    Sorlie, T
    Eisen, MB
    van de Rijn, M
    Jeffrey, SS
    Rees, CA
    Pollack, JR
    Ross, DT
    Johnsen, H
    Akslen, LA
    Fluge, O
    Pergamenschikov, A
    Williams, C
    Zhu, SX
    Lonning, PE
    Borresen-Dale, AL
    Brown, PO
    Botstein, D
    [J]. NATURE, 2000, 406 (6797) : 747 - 752
  • [49] High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
    Pinkel, D
    Seagraves, R
    Sudar, D
    Clark, S
    Poole, I
    Kowbel, D
    Collins, C
    Kuo, WL
    Chen, C
    Zhai, Y
    Dairkee, SH
    Ljung, BM
    Gray, JW
    Albertson, DG
    [J]. NATURE GENETICS, 1998, 20 (02) : 207 - 211
  • [50] Pisani P, 1999, INT J CANCER, V83, P18, DOI 10.1002/(SICI)1097-0215(19990924)83:1&lt