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Species differences in substrate specificity of pyrimidine nucleoside phosphorylase.

作者信息

Maehara Y, Sakaguchi Y, Kusumoto T, Kusumoto H, Sugimachi K

机构信息

Cancer Center of Kyushu University Hospital, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

J Surg Oncol. 1989 Nov;42(3):184-6. doi: 10.1002/jso.2930420311.

DOI:10.1002/jso.2930420311
PMID:2811382
Abstract

To compare the activity of pyrimidine nucleoside phosphorylase (PNP), an enzyme involved in the metabolism of 5-fluorouracil (5-FU), we used uridine (Urd), deoxyuridine (dUrd), and thymidine (dThd) as substrates and human, rat, and mouse neoplastic and normal tissues. As PNP activity was higher in the tumor tissues than in the normal ones in all species examined, the level of PNP activity is expected to be one critical factor linked to the effectiveness of 5-FU. In rats and mice, the ratio of the activities of Urd, dUrd, and dThd was about 10:7:1, whereas in humans, the ratio was 1:30:20. The main enzyme of PNP is Urd phosphorylase in rodents and dThd phosphorylase in humans. Therefore, when examining the metabolism of 5-FU and its analogues for potential clinical application, human tissues should be used.

摘要

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