Mechanisms of anticancer drug resistance

被引:39
作者
Bergman, PJ
机构
[1] Anim Med Ctr, Donaldson Atwood Canc Clin, New York, NY 10021 USA
[2] Anim Med Ctr, Flaherty Comparat Oncol Lab, New York, NY 10021 USA
关键词
D O I
10.1016/S0195-5616(03)00004-4
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Chemotherapy agents are extremely important in the treatment of liquid malignancies, such as lymphoma, myeloma, and chronic lymphocytic leukemia. In addition, chemotherapy agents have proven effective in the adjuvant treatment of solid tumors, such as osteosarcoma, hemangiosarcoma, transitional cell carcinoma, and others. Unfortunately, chemotherapy resistance in these situations is the most significant cause of treatment failure. Therefore, the ability to predict, treat, or circumvent resistance is extremely likely to improve clinical outcomes. This article reviews the most widely investigated forms of chemotherapy resistance, such as reduced drug accumulation, increased DNA damage repairs decreased apoptosis, and others; however, new mechanisms are being found at an alarming pace. In addition, investigations to date have routinely centered on single-cell mechanisms of drug resistance, and cancer is truly a three-dimensional disease. The elucidation of mechanisms surrounding (1) how tumors interact with their surrounding normal microenvironment, (2) how tumors interact in a three-dimensional environment, and (3) a better understanding of basic tumor physiology and biology may supersede in importance those previously elucidated single-cell mechanisms of chemoresistance.
引用
收藏
页码:651 / +
页数:18
相关论文
共 135 条
  • [1] THE ROLE OF DNA TOPOISOMERASES-II IN DRUG-RESISTANCE
    ALTON, PA
    HARRIS, AL
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1993, 85 (02) : 241 - 245
  • [2] ALTUVIA S, 1993, J BIOL CHEM, V268, P27127
  • [3] DEPLETION OF O6-ALKYLGUANINE-DNA ALKYLTRANSFERASE CORRELATES WITH POTENTIATION OF TEMOZOLOMIDE AND CCNU TOXICITY IN HUMAN TUMOR-CELLS
    BAER, JC
    FREEMAN, AA
    NEWLANDS, ES
    WATSON, AJ
    RAFFERTY, JA
    MARGISON, GP
    [J]. BRITISH JOURNAL OF CANCER, 1993, 67 (06) : 1299 - 1302
  • [4] PLEIOTROPIC, MULTIDRUG-RESISTANT PHENOTYPE AND P-GLYCOPROTEIN - A REVIEW
    BAN, T
    [J]. CHEMOTHERAPY, 1992, 38 (03) : 191 - 196
  • [5] Myeloprotection with drug-resistance genes
    Banerjee, D
    Bertino, JR
    [J]. LANCET ONCOLOGY, 2002, 3 (03) : 154 - 158
  • [6] Apoptosis induction of POS canine osteosarcoma cells by vitamin D and retinoids
    Barroga, EF
    Kadosawa, T
    Asano, K
    Okumura, M
    Fujinaga, T
    [J]. JOURNAL OF VETERINARY MEDICAL SCIENCE, 1998, 60 (11) : 1269 - 1272
  • [7] The blood-brain barrier and oncology: new insights into function and modulation
    Bart, J
    Groen, HJM
    Hendrikse, NH
    van der Graaf, WTA
    Vaalburg, W
    de Vries, EGE
    [J]. CANCER TREATMENT REVIEWS, 2000, 26 (06) : 449 - 462
  • [8] Beck WT, 1996, CANCER RES, V56, P3010
  • [9] ALTERED DNA TOPOISOMERASE-II IN MULTIDRUG-RESISTANCE
    BECK, WT
    DANKS, MK
    WOLVERTON, JS
    GRANZEN, B
    CHEN, M
    SCHMIDT, CA
    BUGG, BY
    FRICHE, E
    SUTTLE, DP
    [J]. CYTOTECHNOLOGY, 1993, 11 (02) : 115 - 119
  • [10] NEW MECHANISMS OF HORMONE-SECRETION - MDR-LIKE GENE-PRODUCTS AS EXTRUSION PUMPS FOR HORMONES
    BECKER, KF
    ALLMEIER, H
    HOLLT, V
    [J]. HORMONE AND METABOLIC RESEARCH, 1992, 24 (05) : 210 - 213