Manda T, Nishigaki F, Mukumoto S, Masuda K, Nakamura T, Shimomura K
Department of Pharmacology, Fujisawa Pharmaceutical Co. Ltd., Osaka, Japan.
Eur J Cancer. 1990 Feb;26(2):93-9. doi: 10.1016/0277-5379(90)90289-6.
The antitumor effects of recombinant human tumor necrosis factor-alpha (rTNF-alpha) and 5-fluorouracil (5-FU) in combination treatment were examined on Meth A fibrosarcoma implanted intradermally in mice. Growth of the tumor was inhibited when rTNF-alpha was given i.v. on day 7 or 11 after implantation, but the effect was countered when 5-FU was additionally given i.p. once a day on days 1-4 after implantation. Conversely, 5-FU given on days 5-8 after implantation augmented the antitumor effects of rTNF-alpha. Injection of carbon particles showed that fine capillaries did not develop in the tumors of mice treated with 5-FU on days 1-4 after implantation, but that a delicate network of capillaries developed in the tumors of both the mice treated with 5-FU on days 5-8 after implantation and the controls given saline. The results show that the timing of 5-FU treatment is important when attempting to enhance the antitumor effects of rTNF-alpha, and suggest that these effects are directly associated with newly formed fine capillaries in the tumor.
研究了重组人肿瘤坏死因子-α(rTNF-α)与5-氟尿嘧啶(5-FU)联合治疗对皮下接种于小鼠的Meth A纤维肉瘤的抗肿瘤作用。在接种后第7天或第11天静脉注射rTNF-α可抑制肿瘤生长,但在接种后第1 - 4天每天腹腔注射一次5-FU时,这种作用会被抵消。相反,在接种后第5 - 8天给予5-FU可增强rTNF-α的抗肿瘤作用。碳粒注射显示,在接种后第1 - 4天接受5-FU治疗的小鼠肿瘤中未形成细毛细血管,而在接种后第5 - 8天接受5-FU治疗的小鼠肿瘤以及给予生理盐水的对照小鼠肿瘤中均形成了精细的毛细血管网络。结果表明,在试图增强rTNF-α的抗肿瘤作用时,5-FU治疗的时机很重要,并且提示这些作用与肿瘤中新形成的细毛细血管直接相关。