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S-腺苷同型半胱氨酸水解酶抑制剂3-脱氮-(+/-)-阿里斯托霉素诱导HL-60细胞分化

Induction of HL-60 cell differentiation by 3-deaza-(+/-)-aristeromycin, an inhibitor of S-adenosylhomocysteine hydrolase.

作者信息

Aarbakke J, Miura G A, Prytz P S, Bessesen A, Slørdal L, Gordon R K, Chiang P K

出版信息

Cancer Res. 1986 Nov;46(11):5469-72.

PMID:3463413
Abstract

The metabolically stable inhibitor of S-adenosylhomocysteine hydrolase (AdoHcyase), 3-deaza-(+/-)-aristeromycin (dzAri) has recently been shown to induce differentiation in HL-60 cells. The present study was undertaken to characterize the cytostatic, cytotoxic, and differentiation inducing properties of dzAri in HL-60 cells and to investigate biochemical consequences of AdoHcyase inhibition. A dye exclusion test and a clonogenic assay were used to test cytotoxic and cytostatic properties. dzAri had reversible cytostatic effects on HL-60 cells at concentrations lower than 10 microM and partially reversible cytotoxic effects above 10 microM. The induction of differentiation was dependent upon concentration and time of exposure, with maximal effect after 6 days incubation with 5-10 microM dzAri. Washout experiments demonstrated that the cells were not committed to differentiation after 48 h of incubation with dzAri. The AdoHcyase of HL-60 cells was inhibited with a Ki of 20 nM. The concentration of S-adenosylhomocysteine increased dose dependently 48 h after incubation with 0.1-100 microM dzAri. The incorporation of [3H]methyl from [methyl-3H]methionine into 5-methylcytosine of DNA was reduced by 26% at 5 microM dzAri. The findings indicate that continuous presence of dzAri is necessary to induce differentiation and inhibit proliferation in HL-60 cells. The inhibition of AdoHcyase perturbs levels of transmethylation metabolites and the incorporation of [3H]methyl into 5-methyl-cytosine of DNA.

摘要

S-腺苷高半胱氨酸水解酶(AdoHcyase)的代谢稳定抑制剂3-脱氮-(±)-阿瑞霉素(dzAri)最近已被证明可诱导HL-60细胞分化。本研究旨在表征dzAri在HL-60细胞中的细胞生长抑制、细胞毒性和分化诱导特性,并研究AdoHcyase抑制的生化后果。采用染料排斥试验和克隆形成试验来测试细胞毒性和细胞生长抑制特性。dzAri在浓度低于10 microM时对HL-60细胞具有可逆的细胞生长抑制作用,在高于10 microM时具有部分可逆的细胞毒性作用。分化诱导取决于暴露的浓度和时间,在与5-10 microM dzAri孵育6天后效果最佳。洗脱实验表明,用dzAri孵育48小时后,细胞并未不可逆地分化。HL-60细胞的AdoHcyase被抑制,Ki为20 nM。用0.1-100 microM dzAri孵育48小时后,S-腺苷高半胱氨酸的浓度呈剂量依赖性增加。在5 microM dzAri时,[甲基-3H]甲硫氨酸中[3H]甲基掺入DNA的5-甲基胞嘧啶的量减少了26%。这些发现表明,持续存在dzAri对于诱导HL-60细胞分化和抑制增殖是必要的。AdoHcyase的抑制扰乱了转甲基代谢物的水平以及[3H]甲基掺入DNA的5-甲基胞嘧啶。

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