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单甲基三氮烯和咪唑并四嗪酮对人白血病细胞系K562血红蛋白合成的诱导作用

Induction of haemoglobin synthesis in the human leukaemia cell line K562 by monomethyltriazenes and imidazotetrazinones.

作者信息

Tisdale M J

出版信息

Biochem Pharmacol. 1985 Jun 15;34(12):2077-82. doi: 10.1016/0006-2952(85)90398-3.

Abstract

The effect of a group of imidazotetrazinones and alkyltriazenes on the growth and the induction of differentiation associated properties in K562 human erythroleukaemia cells has been investigated. Only 8-carbamoyl-3-methylimidazo[5,1-d]-1,2,3,5-tetrazin-4(3H)-one and a monomethyltriazene induced the formation of benzidine-positive cells, and a linear relationship was observed between growth inhibition and the percentage of haemoglobin producing cells in the culture. However, growth inhibition alone was insufficient for induction of haemoglobin synthesis since other members of the series inhibited growth without substantially increasing the number of haemoglobin-producing cells. Induction was accompanied by an increase in cell size, and appeared not to arise by selective toxicity to the original non-differentiated cell compartment followed by clonal expansion of the differentiated cells. These results suggest that methylating agents are more effective than ethylating agents in the alteration of gene expression.

摘要

研究了一组咪唑并四嗪酮和烷基三嗪对K562人红白血病细胞生长及诱导分化相关特性的影响。只有8-氨基甲酰基-3-甲基咪唑并[5,1-d]-1,2,3,5-四嗪-4(3H)-酮和一种单甲基三嗪诱导形成联苯胺阳性细胞,并且在生长抑制与培养物中产生血红蛋白细胞的百分比之间观察到线性关系。然而,仅生长抑制不足以诱导血红蛋白合成,因为该系列的其他成员抑制生长而没有实质性增加产生血红蛋白细胞的数量。诱导伴随着细胞大小的增加,并且似乎不是通过对原始未分化细胞区室的选择性毒性随后分化细胞的克隆扩增而产生的。这些结果表明,在基因表达改变方面,甲基化剂比乙基化剂更有效。

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