二氢叶酸还原酶
反叶绿体
胸苷酸合酶
核苷酸还原酶
酶
生物化学
化学
丝氨酸羟甲基转移酶
嘌呤代谢
嘧啶代谢
酶抑制剂
IC50型
核苷酸
嘌呤
抗代谢物
生物
体外
丝氨酸
核苷酸
毒性
有机化学
基因
蛋白质亚单位
化疗
氟尿嘧啶
遗传学
作者
C Shih,V J Chen,Lynn S. Gossett,Susan B. Gates,W.C. MacKellar,Lillian L. Habeck,Katherine A. Shackelford,L G Mendelsohn,D J Soose,Vinod F. Patel,Sherri L. Andis,Jesse R. Bewley,Elizabeth A. Rayl,Barbara A. Moroson,G. Peter Beardsley,William Köhler,Manohar Ratnam,Richard M. Schultz
出处
期刊:PubMed
日期:1997-03-15
卷期号:57 (6): 1116-23
被引量:561
摘要
N-[4-[2-(2-amino-3,4-dihydro-4-oxo-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl ]-benzoyl]-L-glutamic acid (LY231514) is a novel pyrrolo[2,3-d]pyrimidine-based antifolate currently undergoing extensive Phase II clinical trials. Previous studies have established that LY231514 and its synthetic gamma-polyglutamates (glu3 and glu5) exert potent inhibition against thymidylate synthase (TS). We now report that LY231514 and its polyglutamates also markedly inhibit other key folate-requiring enzymes, including dihydrofolate reductase (DHFR) and glycinamide ribonucleotide formyltransferase (GARFT). For example, the Ki values of the pentaglutamate of LY231514 are 1.3, 7.2, and 65 nM for inhibition against TS, DHFR, and GARFT, respectively. In contrast, although a similar high level of inhibitory potency was observed for the parent monoglutamate against DHFR (7.0 nM), the inhibition constants (Ki) for the parent monoglutamate are significantly weaker for TS (109 nM) and GARFT (9,300 nM). The effects of LY231514 and its polyglutamates on aminoimidazole carboxamide ribonucleotide formyltransferase, 5,10-methylenetetrahydrofolate dehydrogenase, and 10-formyltetrahydrofolate synthetase were also evaluated. The end product reversal studies conducted in human cell lines further support the concept that multiple enzyme-inhibitory mechanisms are involved in cytotoxicity. The reversal pattern of LY231514 suggests that although TS may be a major site of action for LY231514 at concentrations near the IC50, higher concentrations can lead to inhibition of DHFR and/or other enzymes along the purine de novo pathway. Studies with mutant cell lines demonstrated that LY231514 requires polyglutamation and transport via the reduced folate carrier for cytotoxic potency. Therefore, our data suggest that LY231514 is a novel classical antifolate, the antitumor activity of which may result from simultaneous and multiple inhibition of several key folate-requiring enzymes via its polyglutamated metabolites.
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