Signal transduction pathway targets for anticancer drug discovery

被引:25
作者
Adjei, AA [1 ]
机构
[1] Mayo Clin, Div Med Oncol, Rochester, MN 55905 USA
关键词
D O I
10.2174/1381612003400821
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
There are currently over 80 agents officially approved for the treatment of cancer world-wide. However, the most common epithelial cancers, which cause greater than 75% of cancer deaths, remain incurable. Most drugs have been developed empirically by testing large numbers of chemicals on rapidly growing transplantable rodent tumors, and more recently, human tumor xenografts. This approach has identified prodeminantly DNA-active drugs that are considerably toxic and have limited efficacy. Novel molecular targets, which are selective for neoplastic cells, are needed for chemotherapeutic agents to improve cure rates of epithelial malignancies, with acceptable toxicity. In recent years, agents inhibiting signal transduction pathway molecules have entered clinical trials. These include antibodies and small molecules, which inhibit growth factor receptors and their receptor tyrosine kinases, inhibitors of cytoplasmic second messengers such as ras, raf and MEK, inhibitors of protein trafficking, and inhibitors of protein degradation.
引用
收藏
页码:361 / 378
页数:18
相关论文
共 124 条
  • [21] c-erbB2 overexpression decreases the benefit of adjuvant tamoxifen in early-stage breast cancer without axillary lymph node metastases
    Carlomagno, C
    Perrone, F
    Gallo, C
    DeLaurentiis, M
    Lauria, R
    Morabito, A
    Pettinato, G
    Panico, L
    DAntonio, A
    Bianco, AR
    DePlacido, S
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (10) : 2702 - 2708
  • [22] Phosphoinositide kinases
    Carpenter, CL
    Cantley, LC
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1996, 8 (02) : 153 - 158
  • [23] Chaudhry A, 1999, CLIN CANCER RES, V5, P3385
  • [24] UCN-01-mediated G1 arrest in normal but not tumor breast cells is pRb-dependent and p53-independent
    Chen, XM
    Lowe, M
    Keyomarsi, K
    [J]. ONCOGENE, 1999, 18 (41) : 5691 - 5702
  • [25] RAPAMYCIN FKBP SPECIFICALLY BLOCKS GROWTH-DEPENDENT ACTIVATION OF AND SIGNALING BY THE 70 KD S6 PROTEIN-KINASES
    CHUNG, J
    KUO, CJ
    CRABTREE, GR
    BLENIS, J
    [J]. CELL, 1992, 69 (07) : 1227 - 1236
  • [26] PDGF-DEPENDENT AND INSULIN-DEPENDENT PP70(S6K) ACTIVATION MEDIATED BY PHOSPHATIDYLINOSITOL-3-OH KINASE
    CHUNG, JK
    GRAMMER, TC
    LEMON, KP
    KAZLAUSKAS, A
    BLENIS, J
    [J]. NATURE, 1994, 370 (6484) : 71 - 75
  • [27] Ciardiello F, 1999, CLIN CANCER RES, V5, P909
  • [28] COBLEIGH MA, 1998, P AN M AM SOC CLIN, V17, pA97
  • [29] COX AD, 1997, BIOCHIM BIOPHYS ACTA, V1333, P51
  • [30] FOS AND JUN - THE AP-1 CONNECTION
    CURRAN, T
    FRANZA, BR
    [J]. CELL, 1988, 55 (03) : 395 - 397