Shiiki S, Fuchimoto S, Iwagaki H, Akazai Y, Matsubara N, Watanabe T, Orita K
First Department of Surgery, Okayama University Medical School, Japan.
Acta Med Okayama. 1991 Oct;45(5):339-45. doi: 10.18926/AMO/32201.
We investigated the antitumor activities of 5-fluorouracil (5-FU), 5'-deoxy-5-fluorouridine (5'-DFUR), 1-hexylcarbamoyl-5-fluorouracil (HCFU) and 1-(tetrahydro-2-furanyl)-5-fluorouracil (FT-207) in combination with hyperthermia in vitro. The antitumor effect of 5-FU (10(-4) M) was slightly enhanced by combination with hyperthermia (42 degrees C) for 2h, and the effect was determined to be additive. Synergistic enhancement of antitumor activity was obtained by the concurrent use of hyperthermia (42 degrees C, 2h) and 5'-DFUR (10(-4) M) or HCFU (10(-5) M). However, the antitumor effect of FT-207 (10(-4) M) in combination with hyperthermia was comparable that of hyperthermia alone. The synergistic enhancement of antitumor activity was not obtained for all drugs when the cells were preheated at 42 degrees C for 2h. On the other hand, when cells were pretreated with drugs before heat exposure, weak interactions were obtained after 5-FU and 5'-DFUR treatment, and a synergistic interaction was obtained after HCFU treatment. It is speculated that the metabolites of 5'-DFUR and HCFU enhance the cytotoxicity of 5-FU, or might change the threshold concentration for a cytotoxic effect of 5-FU in cancer cells.
我们研究了5-氟尿嘧啶(5-FU)、5'-脱氧-5-氟尿苷(5'-DFUR)、1-己基氨基甲酰基-5-氟尿嘧啶(HCFU)和1-(四氢-2-呋喃基)-5-氟尿嘧啶(FT-207)与热疗联合应用时的体外抗肿瘤活性。5-FU(10⁻⁴ M)与42℃热疗联合2小时后,其抗肿瘤作用略有增强,且该作用为相加作用。同时使用42℃热疗(2小时)和5'-DFUR(10⁻⁴ M)或HCFU(10⁻⁵ M)可获得抗肿瘤活性的协同增强。然而,FT-207(10⁻⁴ M)与热疗联合的抗肿瘤作用与单独热疗相当。当细胞在42℃预热2小时时,并非所有药物都能获得抗肿瘤活性的协同增强。另一方面,当细胞在热暴露前用药物预处理时,5-FU和5'-DFUR处理后有微弱相互作用,而HCFU处理后有协同相互作用。据推测,5'-DFUR和HCFU的代谢产物增强了5-FU的细胞毒性,或者可能改变了5-FU在癌细胞中产生细胞毒性作用的阈值浓度。