Inhibition of angiogenesis and invasion in malignant gliomas

被引:46
作者
Chi, Andrew [1 ]
Norden, Andrew D. [1 ]
Wen, Patrick Y. [1 ]
机构
[1] Brigham & Womens Hosp, Dept Neurol, Dana Farber Brigham & Womens Canc Ctr, Div Neurooncol,Ctr Neurooncol, Boston, MA 02115 USA
关键词
angiogenesis; glioblastoma; invasion; malignant glioma; targeted molecular therapy;
D O I
10.1586/14737140.7.11.1537
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant gliomas confer a dismal prognosis. As the molecular events that underlie tumor angiogenesis are elucidated, angiogenesis inhibition is emerging as a promising therapy for recurrent and newly diagnosed tumors. Data from animal studies suggest that angiogenesis inhibition may promote an invasive phenotype in tumor cells. This may represent an important mechanism of resistance to antiangiogenic therapies. Recent studies have begun to clarify the mechanisms by which glioma cells detach from the tumor mass, remodel the extracellular matrix and infiltrate normal brain. An array of potential therapeutic targets exists. Combination therapy with antiangiogenic and novel anti-invasion agents is a promising approach that may produce a synergistic antitumor effect and a survival benefit for patients with these devastating tumors.
引用
收藏
页码:1537 / 1560
页数:24
相关论文
共 294 条
  • [71] FOLKMAN J, 1971, NEW ENGL J MED, V285, P1182
  • [72] WHAT IS THE EVIDENCE THAT TUMORS ARE ANGIOGENESIS DEPENDENT
    FOLKMAN, J
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1990, 82 (01): : 4 - 6
  • [73] Fong TAT, 1999, CANCER RES, V59, P99
  • [74] Gelatinase-A (MMP-2), gelatinase-B (MMP-9) and membrane type matrix metalloproteinase-1 (MT1-MMP) are involved in different aspects of the pathophysiology of malignant gliomas
    Forsyth, PA
    Wong, H
    Laing, TD
    Rewcastle, NB
    Morris, DG
    Muzik, H
    Leco, KJ
    Johnston, RN
    Brasher, PMA
    Sutherland, G
    Edwards, DR
    [J]. BRITISH JOURNAL OF CANCER, 1999, 79 (11-12) : 1828 - 1835
  • [75] Forsythe JA, 1996, MOL CELL BIOL, V16, P4604
  • [76] Zd6474, an inhibitor of VEGFR and EGFR tyrosine kinase activity in combination with radiotherapy
    Frederick, B
    Gustafson, D
    Bianco, C
    Ciardiello, F
    Dimery, I
    Raben, D
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2006, 64 (01): : 33 - 37
  • [77] Gene expression profiling of gliomas strongly predicts survival
    Freije, WA
    Castro-Vargas, FE
    Fang, ZX
    Horvath, S
    Cloughesy, T
    Liau, LM
    Mischel, PS
    Nelson, SF
    [J]. CANCER RESEARCH, 2004, 64 (18) : 6503 - 6510
  • [78] Cathepsin D is a potential serum marker for poor prognosis in glioma patients
    Fukuda, ME
    Iwadate, Y
    Machida, T
    Hiwasa, T
    Nimura, Y
    Nagai, Y
    Takiguchi, M
    Tanzawa, H
    Yamaura, A
    Seki, N
    [J]. CANCER RESEARCH, 2005, 65 (12) : 5190 - 5194
  • [79] Fulton D, 1996, J NEURO-ONCOL, V27, P149
  • [80] Furukawa K, 2006, INT J ONCOL, V29, P73