Kanai T, Konno H, Tanaka T, Baba M, Matsumoto K, Nakamura S, Yukita A, Asano M, Suzuki H, Baba S
Second Department of Surgery, Hamamatsu University School of Medicine, Japan.
Int J Cancer. 1998 Sep 11;77(6):933-6. doi: 10.1002/(sici)1097-0215(19980911)77:6<933::aid-ijc23>3.0.co;2-0.
In order to determine whether the inhibition of vascular-endothelial-growth-factor (VEGF) activity by administration of an immunoneutralizing antibody could suppress tumor growth and metastasis in spontaneous metastatic models of human colon and gastric carcinoma, 4 human carcinoma xenografts, 2 human colon carcinomas (TK4 and TK 13) and 2 gastric carcinomas (MT2 and MT5) were transplanted orthotopically into nude mice. The anti-VEGF antibody (MV833, 100 microg/mouse) or the same volume of saline was administered i.p. on alternative days from day 10 after transplantation. With each of the 4 xenografts, administration of MV833 significantly inhibited not only primary tumor growth but also macroscopic liver metastasis, although the growth rate varied. The inhibitory effect of MV833 on primary tumor growth appeared to have no correlation with the level of VEGF in tumor. Body-weight gain in each treated group was comparable with that in the control group. No toxicity of the antibody was observed. These results suggest that an anti-VEGF antibody can be effective against a wide variety of cancers, and that VEGF may be a possible target for cancer therapy.
为了确定给予免疫中和抗体抑制血管内皮生长因子(VEGF)活性是否能抑制人结肠癌和胃癌自发转移模型中的肿瘤生长和转移,将4种人癌异种移植物,2种人结肠癌(TK4和TK13)和2种胃癌(MT2和MT5)原位移植到裸鼠体内。从移植后第10天起,每隔一天腹腔注射抗VEGF抗体(MV833,100μg/小鼠)或相同体积的生理盐水。对于4种异种移植物中的每一种,MV833的给药不仅显著抑制了原发性肿瘤的生长,还显著抑制了肉眼可见的肝转移,尽管生长速率有所不同。MV833对原发性肿瘤生长的抑制作用似乎与肿瘤中VEGF的水平无关。每个治疗组的体重增加与对照组相当。未观察到该抗体的毒性。这些结果表明,抗VEGF抗体可能对多种癌症有效,并且VEGF可能是癌症治疗的一个潜在靶点。