Therapeutic efficacy of endostatin exhibits a biphasic dose-response curve

被引:110
作者
Celik, I
Sürfücü, O
Dietz, C
Heymach, JV
Force, J
Höschele, I
Becker, CM
Folkman, J
Kisker, O
机构
[1] Univ Marburg, Dept Gen Surg, Univ Marburg Hosp, D-35043 Marburg, Germany
[2] Charite, Dept Obstet & Gynecol, Berlin, Germany
[3] Harvard Univ, Sch Med, Vasc Biol Program, Childrens Hosp, Boston, MA USA
[4] Harvard Univ, Sch Med, Dept Surg, Childrens Hosp, Boston, MA USA
[5] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Obstet & Gynecol, Boston, MA USA
[6] Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
D O I
10.1158/0008-5472.CAN-05-2617
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
We show here that recombinant endostatin protein has a biphasic effect on the inhibition of endothelial cell migration in vitro. In tumor-bearing animals, there is a similar biphasic effect on the inhibition of tumor growth and on circulating endothelial cells after once-daily s.c. injections. This biphasic effect is revealed as a U-shaped curve in which efficacy is optimal between very low and very high doses depending on the tumor type. This result may be applicable to other inhibitors of endothelial growth and to angiogenesis. Furthermore, these results have important implications for clinicians who administer angiogenesis inhibitors for cancer or other allgiogenesis-dependent diseases. When these results are taken together with two previous reports of angiogenesis inhibitors with a U-shaped dose-response, they suggest that other regulators of endothelial growth may display a similar pattern.
引用
收藏
页码:11044 / 11050
页数:7
相关论文
共 49 条
[1]
Endostatin's antiangiogenic signaling network [J].
Abdollahi, A ;
Hahnfeldt, P ;
Maercker, C ;
Gröne, HJ ;
Debus, J ;
Ansorge, W ;
Folkman, J ;
Hlatky, L ;
Huber, PE .
MOLECULAR CELL, 2004, 13 (05) :649-663
[2]
VEGF contributes to postnatal neovascularization by mobilizing bone marrow-derived endothelial progenitor cells [J].
Asahara, T ;
Takahashi, T ;
Masuda, H ;
Kalka, C ;
Chen, DH ;
Iwaguro, H ;
Inai, Y ;
Silver, M ;
Isner, JM .
EMBO JOURNAL, 1999, 18 (14) :3964-3972
[3]
Benelli R, 2003, INT J ONCOL, V22, P87
[4]
Rapamycin-induced endothelial cell death and tumor vessel thrombosis potentiate cytotoxic therapy against pancreatic cancer [J].
Bruns, CJ ;
Koehl, GE ;
Guba, M ;
Yezhelyev, M ;
Steinbauer, M ;
Seeliger, H ;
Schwend, A ;
Hoehn, A ;
Jauch, KW ;
Geissler, EK .
CLINICAL CANCER RESEARCH, 2004, 10 (06) :2109-2119
[5]
Quantitative analysis of biomarkers defines an optimal biological dose for recombinant human endostatin in primary human tumors [J].
Davis, DW ;
Shen, Y ;
Mullani, NA ;
Wen, S ;
Herbst, RS ;
O'Reilly, M ;
Abbruzzese, JL ;
McConkey, DJ .
CLINICAL CANCER RESEARCH, 2004, 10 (01) :33-42
[6]
Unfulfilled promise of endostatin in a gene therapy-xenotransplant model of human acute lymphocytic leukemia [J].
Eisterer, W ;
Jiang, XY ;
Bachelot, T ;
Pawliuk, R ;
Abramovich, C ;
Leboulch, P ;
Hogge, D ;
Eaves, C .
MOLECULAR THERAPY, 2002, 5 (04) :352-359
[7]
Angiostatin and endostatin inhibit endothelial cell migration in response to FGF and VEGF without interfering with specific intracellular signal transduction pathways [J].
Eriksson, K ;
Magnusson, P ;
Dixelius, J ;
Claesson-Welsh, L ;
Cross, MJ .
FEBS LETTERS, 2003, 536 (1-3) :19-24
[8]
FOLKMAN J, 2003, CANC MED, V6, P161
[9]
The antitumoral effect of endostatin and angiostatin is associated with a down-regulation of vascular endothelial growth factor expression in tumor cells [J].
Hajitou, A ;
Grignet-Debrus, C ;
Devy, L ;
Berndt, S ;
Blacher, S ;
Deroanne, CF ;
Bajou, K ;
Fong, T ;
Chiang, YW ;
Foidart, JM ;
Noël, A .
FASEB JOURNAL, 2002, 16 (11) :1802-+
[10]
Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis [J].
Hanahan, D ;
Folkman, J .
CELL, 1996, 86 (03) :353-364