Kuwa K, Sakamoto S, Sassa S, Yoshimura S, Maemura M, Nakayama T
Medical Research Institute, Tokyo Medical and Dental University, Japan.
Anticancer Res. 1999 Nov-Dec;19(6B):5139-42.
Thymidylate synthase and thymidine kinase are key enzymes involved in the de novo and salvage pathways for pyrimidine nucleotide synthesis, respectively. Thymidylate synthase is inhibited by 5-fluorodeoxyuridine monophosphate, forming an inactive ternary complex with intracellular folate. We investigated the effects of 1-(2-tetrahydrofuryl)-5-FU plus uracil (UFT) with or without leucovorin on 1,2-dimethylhydrazine-induced rat colorectal carcinomas. Thirty-week administration of UFT with or without leucovorin markedly suppressed both colorectal carcinogenesis and tumor growth, resulted in the increase of thymidylate synthase inhibition and the decrease of thymidine kinase activity in the tumor cells. These results indicate that the combination of UFT with leucovorin could be useful in the development of pre- and post-operative adjuvant chemotherapy programs.
胸苷酸合成酶和胸苷激酶分别是参与嘧啶核苷酸从头合成途径和补救途径的关键酶。胸苷酸合成酶被5-氟脱氧尿苷单磷酸抑制,与细胞内叶酸形成无活性的三元复合物。我们研究了1-(2-四氢呋喃基)-5-氟尿嘧啶加尿嘧啶(UFT)联合或不联合亚叶酸对1,2-二甲基肼诱导的大鼠结直肠癌的影响。连续30周给予UFT联合或不联合亚叶酸显著抑制了结直肠癌的发生和肿瘤生长,导致肿瘤细胞中胸苷酸合成酶抑制作用增强和胸苷激酶活性降低。这些结果表明,UFT与亚叶酸联合应用可能有助于术前和术后辅助化疗方案的制定。