Synergistic antitumor effect of an angiogenesis inhibitor (TNP-470) and tumor necrosis factor in mice

被引:4
作者
Amikura, Katsumi [1 ]
Matsuno, Seiki [1 ]
Egawa, Shinichi [1 ]
机构
[1] Tohoku Univ, Sch Med, Dept Surg 1, Aoba Ku, Sendai, Miyagi 9808574, Japan
关键词
TNP-470; tumor necrosis factor; angiogenesis inhibitor; mouse;
D O I
10.1007/s00595-006-3289-3
中图分类号
R61 [外科手术学];
学科分类号
摘要
Purpose. We investigated the potentiation of combination therapy using tumor necrosis factor (TNF) with TNP-470, a potent angiogenesis inhibitor. Methods. We evaluated the antitumor effect in vivo against subcutaneous (s.c.) MC38 mouse colon adenocarcinoma tumors in C57BL/6 mice. The mice were treated with a single bolus injection via the tail vein of 3 or 8 mu g rhTNF in 0.5% bovine serum albumin/normal saline (BSA/NS), or with 0.5% BSA/NS alone as a control, with or without TNP-470 pretreatment, given as 30 or 60mg/kg x 2 days, s.c. DNA synthesis in human umbilical endothelial cells (HUVEC) was assessed by [H-3]thymidine uptake after incubation with TNF, with or without TNP-470. Results. The antitumor effect of TNP-470 pretreatment combined with 3 mu g recombinant human (rh) TNF injection resulted in an 80% reduction of tumor volume compared with the control. This was significantly better than that induced by 3 mu g rhTNF alone (P < 0.005). DNA synthesis in HUVEC was inhibited by TNF with TNP-470 in a dose-dependent manner, but there was no enhanced effect against MC38 in vitro. Conclusions. These results suggest that the combination of the angiogenesis inhibitor TNP-470 and TNF might have a synergistic antitumor effect on solid tumors in vivo.
引用
收藏
页码:1069 / 1074
页数:6
相关论文
共 24 条
[1]  
ABE J, 1994, CANCER RES, V54, P3407
[2]  
Amikura K., 1995, Proceedings of the American Association for Cancer Research Annual Meeting, V36, P468
[3]  
ASHER A, 1987, J IMMUNOL, V138, P963
[4]  
Bhargava P, 1999, CLIN CANCER RES, V5, P1989
[5]  
CLAUSS M, 1990, J BIOL CHEM, V265, P7078
[6]   VASCULAR-PERMEABILITY FACTOR - A TUMOR-DERIVED POLYPEPTIDE THAT INDUCES ENDOTHELIAL-CELL AND MONOCYTE PROCOAGULANT ACTIVITY, AND PROMOTES MONOCYTE MIGRATION [J].
CLAUSS, M ;
GERLACH, M ;
GERLACH, H ;
BRETT, J ;
WANG, F ;
FAMILLETTI, PC ;
PAN, YCE ;
OLANDER, JV ;
CONNOLLY, DT ;
STERN, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (06) :1535-1545
[7]  
Coley W.B., 1893, AM J MED SCI, V105, P487, DOI DOI 10.1097/00000441-189305000-00001
[8]  
FRAKER DL, 1994, CANC PRINCIPLES PRAC, P179
[9]   ENHANCED RESPONSIVENESS OF ENDOTHELIUM IN THE GROWING MOTILE STATE TO TUMOR NECROSIS FACTOR CACHECTIN [J].
GERLACH, H ;
LIEBERMAN, H ;
BACH, R ;
GODMAN, G ;
BRETT, J ;
STERN, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (03) :913-931
[10]   SYNTHETIC ANALOGS OF FUMAGILLIN THAT INHIBIT ANGIOGENESIS AND SUPPRESS TUMOR-GROWTH [J].
INGBER, D ;
FUJITA, T ;
KISHIMOTO, S ;
SUDO, K ;
KANAMARU, T ;
BREM, H ;
FOLKMAN, J .
NATURE, 1990, 348 (6301) :555-557