Kubota Tetsuro
Department of Surgery, School of Medicine, Keio University, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.
Int J Clin Oncol. 2003 Jun;8(3):127-31. doi: 10.1007/s10147-003-0319-7.
Dihydropyrimidine dehydrogenase (DPD) is a rate-limiting enzyme of (fluorinated) pyrimidine degradation that plays a significant role in the pharmacokinetics of 5-fluorouracil (5-FU). In addition, a catabolite of 5-FU induces a certain toxicity, and the sensitivity of 5-FU is determined by DPD activity in tumors. DPD is thus important clinically. Drugs have been developed that control variations of the pharmacokinetics of 5-FU by controlling or inhibiting DPD, thereby reducing toxicity and improving sensitivity. These fluorinated pyrimidines with DPD-inhibiting activity, called DPD-inhibitory fluoropyrimidines, contribute to oral therapy with 5-FU for cancer. This paper summarizes the important role of DPD in cancer chemotherapy with 5-FU.
二氢嘧啶脱氢酶(DPD)是(氟化)嘧啶降解的限速酶,在5-氟尿嘧啶(5-FU)的药代动力学中起重要作用。此外,5-FU的一种分解代谢产物会诱发一定的毒性,5-FU的敏感性由肿瘤中的DPD活性决定。因此,DPD在临床上很重要。已经开发出通过控制或抑制DPD来控制5-FU药代动力学变化的药物,从而降低毒性并提高敏感性。这些具有DPD抑制活性的氟化嘧啶,称为DPD抑制性氟嘧啶,有助于5-FU用于癌症的口服治疗。本文总结了DPD在5-FU癌症化疗中的重要作用。