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在筛选含有单个疱疹病毒胸苷激酶基因的耐药人类细胞的过程中,观察到了与9-(1,3-二羟基-2-丙氧甲基)鸟嘌呤相关的细胞毒性作用。

A cytotoxic effect associated with 9-(1,3-dihydroxy-2-propoxymethyl)-guanine is observed during the selection for drug resistant human cells containing a single herpesvirus thymidine kinase gene.

作者信息

Goring D R, DuBow M S

出版信息

Biochem Biophys Res Commun. 1985 Nov 27;133(1):195-201. doi: 10.1016/0006-291x(85)91860-1.

Abstract

A cytotoxic effect associated with 9-(1,3-dihydroxy-2-propoxymethyl)-guanine (DHPG) was discovered while searching for spontaneous mutations in a single copy, integrated HSV-1 thymidine kinase (TK) gene in the human 143 TK- cell line. It was found that spontaneous DHPGR mutations could not be selected while other anti-TK drugs resulted in selectable mutation frequencies of 10(-4) to 10(-3). When 143 TK- cells were mixed with these HSV-1 TK+ cells and subjected to DHPG, a 90% to 100% decrease in recoverable TK- colonies was observed. In addition, the media from the HSV-1 TK+ cells metabolizing DHPG was shown to inhibit the growth of the TK- cells.

摘要

在人类143 TK-细胞系中寻找单拷贝整合型单纯疱疹病毒1型(HSV-1)胸苷激酶(TK)基因的自发突变时,发现了与9-(1,3-二羟基-2-丙氧基甲基)-鸟嘌呤(DHPG)相关的细胞毒性作用。结果发现,无法筛选出自发性DHPGR突变,而其他抗TK药物导致的可筛选突变频率为10^(-4)至10^(-3)。当143 TK-细胞与这些HSV-1 TK+细胞混合并施加DHPG时,可回收的TK-集落减少了90%至100%。此外,来自代谢DHPG的HSV-1 TK+细胞的培养基被证明可抑制TK-细胞的生长。

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