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6-巯基嘌呤和6-硫鸟嘌呤在中国仓鼠卵巢细胞中的不同作用。

Dissimilar actions of 6-mercaptopurine and 6-thioguanine in Chinese hamster ovary cells.

作者信息

Maybaum J, Hink L A, Roethel W M, Mandel H G

出版信息

Biochem Pharmacol. 1985 Oct 15;34(20):3677-82. doi: 10.1016/0006-2952(85)90230-8.

Abstract

The actions of 6-thioguanine (TG) and 6-mercaptopurine (MP) were compared in Chinese hamster ovary (CHO) cells. Several differences were noted between these two agents. TG caused a greater maximal loss of clonogenicity, leaving about one log fewer survivors than did MP, although the cells killed by MP appeared to succumb much more rapidly than those killed by TG. MP-treated populations experienced a G1 or G1/S arrest which was quickly reversed upon drug removal, while TG-treated cells were arrested in late S/G2, after some delay. Although TG induced a gross chromosome deformation [unilateral chromatid damage, as described earlier in Maybaum and Mandel, Cancer Res. 43, 3852 (1983)] MP caused little or no such deformation. Addition of 4-amino-5-imidazolecarboxamide (AIC) to MP treatments antagonized MP-induced loss of clonogenicity, while AIC caused a dose-dependent potentiation of TG-induced loss of clonogenicity. The interaction between TG and AIC does not seem to represent an increase in either purine starvation or incorporation of TG into DNA, suggesting that a third mechanism is involved. We suggest that this additional mechanism may possibly be related to the induction of differentiation by TG that has been reported in other systems.

摘要

比较了6-硫鸟嘌呤(TG)和6-巯基嘌呤(MP)在中国仓鼠卵巢(CHO)细胞中的作用。发现这两种药物存在一些差异。TG导致更大的克隆形成能力最大损失,存活细胞比MP处理组少约一个对数,尽管MP杀死的细胞似乎比TG杀死的细胞更快死亡。MP处理的细胞群体经历G1或G1/S期阻滞,去除药物后迅速逆转,而TG处理的细胞在延迟一段时间后阻滞在S/G2晚期。尽管TG诱导明显的染色体变形[如Maybaum和Mandel先前在《癌症研究》43, 3852 (1983)中所述的单侧染色单体损伤],但MP几乎没有引起这种变形。在MP处理中添加4-氨基-5-咪唑甲酰胺(AIC)可拮抗MP诱导的克隆形成能力损失,而AIC导致TG诱导的克隆形成能力损失呈剂量依赖性增强。TG与AIC之间的相互作用似乎并不代表嘌呤饥饿增加或TG掺入DNA增加,提示涉及第三种机制。我们认为这种额外的机制可能与其他系统中报道的TG诱导分化有关。

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