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3-去氮腺苷对小鼠红白血病细胞分化的抑制作用。

Inhibition of murine erythroleukemia cell differentiation by 3-deazaadenosine.

作者信息

Sherman M L, Shafman T D, Spriggs D R, Kufe D W

出版信息

Cancer Res. 1985 Nov;45(11 Pt 2):5830-4.

PMID:3863710
Abstract

Recent studies have demonstrated that 5'-methylthioadenosine, an inhibitor of S-adenosylhomocysteine (AdoHcy) hydrolase, blocks induction of murine erythroleukemia cell (MEL) differentiation. The nucleoside analogue 3-deazaadenosine (c3Ado) is both an efficient substrate and a potent inhibitor of AdoHcy hydrolase. The present study was undertaken to determine whether c3Ado would similarly inhibit MEL differentiation. The results demonstrate that c3Ado inhibits induction of MEL differentiation by dimethyl sulfoxide, hexamethylene bisacetamide, butyric acid, and diazapam. c3Ado blocks the appearance of the differentiated MEL phenotype by inhibiting both MEL heme synthesis and transcription of alpha- and beta-globin RNA. The inhibitory effect of c3Ado on MEL differentiation is concentration dependent, reversible, and potentiated by L-homocysteine thiolactone. Furthermore the AdoHcy/AdoMet ratio increases nearly 3.5-fold after 24 h of treatment with 50 microM c3Ado. In contrast, this c3Ado effect is not associated with polyamine depletion or cytostasis. These findings indicate that c3Ado blocks the induction of MEL differentiation at a transcriptional level and that this effect may be related to inhibition of AdoHcy hydrolase.

摘要

最近的研究表明,5'-甲硫腺苷作为S-腺苷同型半胱氨酸(AdoHcy)水解酶的抑制剂,可阻断小鼠红白血病细胞(MEL)分化的诱导。核苷类似物3-去氮腺苷(c3Ado)既是AdoHcy水解酶的有效底物,也是其强效抑制剂。本研究旨在确定c3Ado是否同样会抑制MEL分化。结果表明,c3Ado可抑制二甲基亚砜、六亚甲基双乙酰胺、丁酸和地西泮诱导的MEL分化。c3Ado通过抑制MEL血红素合成以及α-和β-珠蛋白RNA的转录,来阻断分化的MEL表型的出现。c3Ado对MEL分化的抑制作用具有浓度依赖性、可逆性,且可被L-同型半胱氨酸硫内酯增强效力。此外,用50 microM c3Ado处理24小时后,AdoHcy/AdoMet比值增加近3.5倍。相比之下,这种c3Ado效应与多胺耗竭或细胞生长停滞无关。这些发现表明,c3Ado在转录水平上阻断MEL分化的诱导,且这种效应可能与抑制AdoHcy水解酶有关。

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