Yoshida M, Hoshi A, Kuretani K
Nucleic Acids Symp Ser. 1980(8):s175-8.
The mechanism of the reversal of 5-fluorouracil cytotoxicity in L5178Y cells by hypoxanthine, adenine and inosine was examined in a cell-free system. A crude extract of the cells possessed high hypoxanthine and adenine phosphoribosyltransferase and purine nucleoside phosphorylase activities. Hypoxanthine (2 mM), adenine (5 mM) and inosine (5 mM) inhibited the nucleotide formation from 5-fluorouracil at 0.2 mM 5-phosphoribosyl 1-pyrophosphate (PRPP). However, at a higher concentration of PRPP (2.5 mM), the inhibition of hypoxanthine was not found. It suggests that the inhibition of 5-fluorouracil metabolism is due to a deficiency of PRPP induced by phosphoribosylation of hypoxanthine and adenine.
在无细胞体系中研究了次黄嘌呤、腺嘌呤和肌苷逆转L5178Y细胞中5-氟尿嘧啶细胞毒性的机制。细胞的粗提取物具有高次黄嘌呤和腺嘌呤磷酸核糖基转移酶以及嘌呤核苷磷酸化酶活性。次黄嘌呤(2 mM)、腺嘌呤(5 mM)和肌苷(5 mM)在0.2 mM 5-磷酸核糖1-焦磷酸(PRPP)存在时抑制了由5-氟尿嘧啶形成核苷酸。然而,在较高浓度的PRPP(2.5 mM)时,未发现次黄嘌呤的抑制作用。这表明5-氟尿嘧啶代谢的抑制是由于次黄嘌呤和腺嘌呤的磷酸核糖基化诱导的PRPP缺乏所致。