Redefining the target: Chemotherapeutics as antiangiogenics

被引:329
作者
Miller, KD [1 ]
Sweeney, CJ [1 ]
Sledge, GW [1 ]
机构
[1] Indiana Univ, Sch Med, Div Hematol & Oncol, Indianapolis, IN 46202 USA
关键词
D O I
10.1200/JCO.2001.19.4.1195
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Angiogenesis, or new blood vessel formation, is now known to play an important role in both growth and metastasis of many cancers. The central importance of angiogenesis and the understanding of how new blood vessels are formed, has led to novel therapies designed to interrupt this process. Though specific antiangiogenic compounds have only recently entered the clinic, they herald a new era, one in which biology is the basis for therapy. The intense interest in angiogenesis has also lead to a re-examination of the activity of many established cytotoxic agents. Claims of antiangiogenic activity abound, unfortunately, with no common criteria and often little evidence of clinical relevance. What are we to think? Have oncologists unknowingly been administering antiangiogenic therapy all these! years? If chemotherapeutics are really antiangiogenics in disguise, why have they failed to cure most solid tumors? Might the hard-learned lessons of chemotherapy resistance pertain to the novel antiangiogenics as well? Though we can offer no certain answers to these important questions, we do offer a framework on which to order the rapidly burgeoning literature. We suggest criteria by which a cytotoxic agent might reasonably be considered to have meaningful antiangiogenic activity. finally, we describe patential mechanisms of resistance to antiangiogenic chemotherapies-some of which may apply to the pure antiangiogenics currently in development.
引用
收藏
页码:1195 / 1206
页数:12
相关论文
共 144 条
  • [1] Aikawa H, 1999, ANTICANCER RES, V19, P4305
  • [2] Albini A, 1998, Pathol Oncol Res, V4, P230
  • [3] Algire GH, 1943, J NATL CANCER I, V4, P1
  • [4] Alonso DF, 1999, INT J CANCER, V83, P242, DOI 10.1002/(SICI)1097-0215(19991008)83:2<242::AID-IJC16>3.0.CO
  • [5] 2-8
  • [6] [Anonymous], CANC C HIGHLIGHTS
  • [7] Taxol involution of collagen-induced arthritis:: Ultrastructural correlation with the inhibition of synovitis and neovascularization
    Arsenault, AL
    Lhoták, S
    Hunter, WL
    Banquerigo, MLC
    Brahn, E
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 86 (03): : 280 - 289
  • [8] Assimakopoulou M, 1997, ANTICANCER RES, V17, P4747
  • [9] TUMOR-INDUCED ANGIOGENESIS - LACK OF INHIBITION BY IRRADIATION
    AUERBACH, R
    ARENSMAN, R
    KUBAI, L
    FOLKMAN, J
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1975, 15 (02) : 241 - 245
  • [10] MIGRATION AND PROLIFERATION OF ENDOTHELIAL CELLS IN PREFORMED AND NEWLY FORMED BLOOD-VESSELS DURING TUMOR ANGIOGENESIS
    AUSPRUNK, DH
    FOLKMAN, J
    [J]. MICROVASCULAR RESEARCH, 1977, 14 (01) : 53 - 65