Application of DNA Microarrays in pharmacogenomics and toxicogenomics

被引:42
作者
Chin, KV [1 ]
Kong, ANT
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Med & Pharmacol, New Brunswick, NJ 08901 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Canc Inst New Jersey, New Brunswick, NJ 08901 USA
[3] Rutgers State Univ, Ernest Mario Sch Pharm, Dept Pharmaceut, Piscataway, NJ 08854 USA
关键词
microarray; pharmacogenomics; toxicogenomics; signal transduction; apoptosis;
D O I
10.1023/A:1021425004264
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Many drugs or xenobiotics can induce specific or nonspecific cellular signal transduction events that activate various physiologic and pharmacologic responses including homeostasis, proliferation, differentiation, apoptosis, and necrosis. To minimize the insults caused by these xenobiotics, tissues and organs are equipped with protective mechanisms that either pump drugs out of the cells (e. g., the multidrug- resistant, mdr, family of proteins) or increase the level of detoxifying enzymes such as phase I and II drug- metabolizing enzymes (DMEs), after exposure to xenobiotics. This review discusses the molecular analysis of pharmaco- or toxicogenomic gene expression profiles following exposure to cancer chemotherapeutic and chemopreventive agents. We present the development of DNA microarray technology and its use in expression profiling of possible signal transduction events elicited by these compounds, and its potential future applications in drug discovery and development in the pharmaceutical industry.
引用
收藏
页码:1773 / 1778
页数:6
相关论文
共 30 条
  • [1] Afshari CA, 1999, CANCER RES, V59, P4759
  • [2] NUMBER OF CPG ISLANDS AND GENES IN HUMAN AND MOUSE
    ANTEQUERA, F
    BIRD, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) : 11995 - 11999
  • [3] 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
  • [4] CLONING OF NRF1, AN NF-E2-RELATED TRANSCRIPTION FACTOR, BY GENETIC SELECTION IN YEAST
    CHAN, JY
    HAN, XL
    KAN, YW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (23) : 11371 - 11375
  • [5] ISOLATION OF CDNA-ENCODING THE HUMAN NF-E2 PROTEIN
    CHAN, JY
    HAN, XL
    KAN, YW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (23) : 11366 - 11370
  • [6] THE TOXICITY OF MENADIONE AND MITOZANTRONE IN HUMAN LIVER-DERIVED HEP G2 HEPATOMA-CELLS
    DUTHIE, SJ
    GRANT, MH
    [J]. BIOCHEMICAL PHARMACOLOGY, 1989, 38 (08) : 1247 - 1255
  • [7] Cluster analysis and display of genome-wide expression patterns
    Eisen, MB
    Spellman, PT
    Brown, PO
    Botstein, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) : 14863 - 14868
  • [8] Mutational analysis using oligonucleotide microarrays
    Hacia, JG
    Collins, FS
    [J]. JOURNAL OF MEDICAL GENETICS, 1999, 36 (10) : 730 - 736
  • [9] HU R, 2001, AAPS PHARMSCI S, V3, P2333
  • [10] Regulation of the antioxidant response element by protein kinase C-mediated phosphorylation of NF-E2-related factor 2
    Huang, HC
    Nguyen, T
    Pickett, CB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) : 12475 - 12480