Abolished angiogenicity and tumorigenicity of rat glioma by 1-naphthalenemonosulfonate

被引:11
作者
Cuevas, P [1 ]
Carceller, F
Diaz, D
Reimers, D
Fernández, M
Lozano, RM
González-Corrochano, R
Giménez-Gallego, G
机构
[1] Hosp Ramon y Cajal, Dept Invest, E-28034 Madrid, Spain
[2] Univ Complutense, CAI Resonancia Magnet Nucl, Inst Pluridisciplinar, E-28040 Madrid, Spain
[3] CSIC, Ctr Invest Biol, Madrid, Spain
关键词
glioma; anti-angiogenic tumor therapy; pro-apoptotic tumor therapy; fibroblast growth factors; 1-naphthalenemonosulfonate;
D O I
10.1016/S0304-3940(01)02006-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Suramins and suradistas, an important group of potential anti-cancer agents, inhibit fibroblast growth factor (FGF) mitogenic activity. It has been shown that naphthalenesulfonates, with a common chemical function to the family of suramins and suradistas, mimic their inhibitory activity, abolishing FGF-induced angiogenesis in vivo, and inducing apoptosis of C6 glioma cells in culture. In the present report, we show that intratumoral administration of 1-naphthalenemonosulfonate induces a considerable regression of gliomas in rats, significantly enhances apoptosis, and attenuates tumor angiogenesis. These findings may lead to new approaches for the treatment of glioblastoma, a most common primary malignant brain tumor of very poor prognosis, as well as of other angiogenesis-dependent malignancies. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:185 / 188
页数:4
相关论文
共 21 条
[1]  
[Anonymous], 1995, The molecular basis of cancer
[2]   APOPTOSIS OF VASCULAR ENDOTHELIAL-CELLS BY FIBROBLAST GROWTH-FACTOR DEPRIVATION [J].
ARAKI, S ;
SHIMADA, Y ;
KAJI, K ;
HAYASHI, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 168 (03) :1194-1200
[3]   SINGLE TOPICAL APPLICATION OF HUMAN RECOMBINANT BASIC FIBROBLAST GROWTH-FACTOR (RBFGF) PROMOTES NEOVASCULARIZATION IN RAT CEREBRAL-CORTEX [J].
CUEVAS, P ;
GIMENEZGALLEGO, G ;
CARCELLER, F ;
CUEVAS, B ;
CRESPO, A .
SURGICAL NEUROLOGY, 1993, 39 (05) :380-384
[4]   Suppression of acidic fibroblast growth factor-dependent angiogenesis by the antigrowth activity of 1,3,6-naphthalenetrisulfonate [J].
Cuevas, P ;
Lozano, RM ;
Giménez-Gallego, G .
NEUROLOGICAL RESEARCH, 1999, 21 (02) :191-194
[5]   Apoptosis of glioma cells induced by the fibroblast growth factor inhibitor 1.3.6-naphthalenetrisulfonate [J].
Cuevas, P ;
Reimers, D ;
Diaz, D ;
Lozano, RM ;
Giménez-Gallego, G .
NEUROSCIENCE LETTERS, 1999, 275 (02) :149-151
[6]   ANGIOGENESIS IN CANCER, VASCULAR, RHEUMATOID AND OTHER DISEASE [J].
FOLKMAN, J .
NATURE MEDICINE, 1995, 1 (01) :27-31
[7]   TUMOR ANGIOGENESIS [J].
FOLKMAN, J .
ADVANCES IN CANCER RESEARCH, 1985, 43 :175-203
[8]  
Fuks Z, 1995, Cancer J Sci Am, V1, P62
[9]   DORMANCY OF MICROMETASTASES - BALANCED PROLIFERATION AND APOPTOSIS IN THE PRESENCE OF ANGIOGENESIS SUPPRESSION [J].
HOLMGREN, L ;
OREILLY, MS ;
FOLKMAN, J .
NATURE MEDICINE, 1995, 1 (02) :149-153
[10]   REGULATORS OF ANGIOGENESIS [J].
KLAGSBRUN, M .
ANNUAL REVIEW OF PHYSIOLOGY, 1991, 53 :217-239