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L-651,582的抗增殖活性与磷酸核糖焦磷酸合成酶处钙介导的核苷酸代谢调节相关。

Anti-proliferative activity of L-651,582 correlates with calcium-mediated regulation of nucleotide metabolism at phosphoribosyl pyrophosphate synthetase.

作者信息

Hupe D J, Behrens N D, Boltz R

机构信息

Department of Enzymology, Merck Institute for Therapeutic Research, Rahway, New Jersey 07065.

出版信息

J Cell Physiol. 1990 Sep;144(3):457-66. doi: 10.1002/jcp.1041440313.

DOI:10.1002/jcp.1041440313
PMID:2167901
Abstract

L-651,582, 5-amino-[4-(4-chlorobenzoyl)-3,5-dichlorobenzyl]-1, 2,3-triazole-4-carboxamide, is an antiproliferative and antiparasitic agent which inhibits nucleotide metabolism in mammalian cells. The drug equivalently inhibited 3H-hypoxanthine, 14C-adenine, and 14C-formate incorporation into nucleotide pools in Madin-Darby bovine kidney (MDBK) cells, suggesting depletion of the supply of phosphoribosyl pyrophosphate, (PRPP), required for each of these independent pathways. Inhibition of nucleotide metabolism correlated with inhibition of proliferation for three cell types with differing sensitivities toward the drug. L-651,582 inhibited incorporation of 3H-hypoxanthine into nucleotide pools with either glucose, uridine, or ribose as carbon source suggesting a block at PRPP synthetase, rather than a block in a pathway supplying ribose-5-phosphate. PRPP synthetase was not inhibited directly by the compound, indicating regulation of the enzyme in intact cells. Drug treatment did not kill cells but reduced the fraction of cells in S and G2/M while increasing the population in G1. Inhibition of uptake of 45Ca was demonstrated at concentrations identical to those required for inhibition of nucleotide metabolism or proliferation. Inhibition of cellular PRPP biosynthesis rates were also observed using EGTA to lower calcium levels. These data suggest a previously unrecognized link between calcium entry, the regulation of nucleotide biosynthesis at PRPP synthetase, and the rate of proliferation of mammalian cells.

摘要

L-651,582,即5-氨基-[4-(4-氯苯甲酰基)-3,5-二氯苄基]-1,2,3-三唑-4-甲酰胺,是一种抗增殖和抗寄生虫药物,可抑制哺乳动物细胞中的核苷酸代谢。该药物同等程度地抑制了3H-次黄嘌呤、14C-腺嘌呤和14C-甲酸掺入麦迪逊-达比牛肾(MDBK)细胞的核苷酸池中,这表明这些独立途径所需的磷酸核糖焦磷酸(PRPP)供应减少。对于三种对该药物敏感性不同的细胞类型,核苷酸代谢的抑制与增殖的抑制相关。L-651,582以葡萄糖、尿苷或核糖作为碳源时,抑制了3H-次黄嘌呤掺入核苷酸池,这表明是在PRPP合成酶处受阻,而不是在供应5-磷酸核糖的途径中受阻。该化合物并未直接抑制PRPP合成酶,这表明在完整细胞中该酶受到调控。药物处理并未杀死细胞,但减少了处于S期和G2/M期的细胞比例,同时增加了G1期的细胞数量。在与抑制核苷酸代谢或增殖所需浓度相同的情况下,证实了对45Ca摄取的抑制。使用乙二醇双四乙酸(EGTA)降低钙水平时,也观察到了细胞PRPP生物合成速率的抑制。这些数据表明,钙内流、PRPP合成酶处核苷酸生物合成的调控与哺乳动物细胞增殖速率之间存在一种以前未被认识到的联系。

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