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依托泊苷诱导的小鼠白血病L1210细胞脱氧核糖核酸(DNA)损伤及其对核苷酸库的影响

[Etoposide-induced deoxyribonucleic acid (DNA) damage and its effects on nucleotide pools in murine leukemia L1210 cells].

作者信息

Ooi K, Ohkubo T, Kawasaki H, Sakurai M

机构信息

Department of Pharmacy, Social Insurance Hazu Hospital, Yokkaichi, Japan.

出版信息

Yakugaku Zasshi. 1990 Sep;110(9):673-7. doi: 10.1248/yakushi1947.110.9_673.

Abstract

The effect of etoposide-induced deoxyribonucleic acid (DNA) damage and its effect on nucleotide pools were examined in murine leukemia L1210 cells. Etoposide (15 mg/kg) was administered intraperitoneally on the third day after peritoneal inoculation of 1 x 10(6) L1210 cells. The dosage of etoposide produced 175% of the increase of lifespan as described previously. Strand breaks in DNA occurred within 10 min after i.p. injection, but as the time interval between injection and removal of the cells from the mice was elongated to 1 and 3 h, the continuous repairing of DNA was observed. At 6 h after the injection, the maximum concentration of DNA was located in the vicinity of that of control. In our previous study, ara-C was most effective when given at 3 to 6 h after the administration of etoposide. The sensitivity to ara-C might increase during the repairing period from the etoposide-induced DNA damage. All four dNTPs increased progressively within 6 h up to 3-fold of control. The changes in rNTPs were similar, but the degree of the changes was smaller than that of dNTPs. These changes in dNTPs and rNTPs would be an important factor for the combination to determine the antitumor effect of etoposide and nucleoside analogues.

摘要

在小鼠白血病L1210细胞中检测了依托泊苷诱导的脱氧核糖核酸(DNA)损伤效应及其对核苷酸库的影响。在腹腔接种1×10⁶个L1210细胞后的第三天,腹腔注射依托泊苷(15mg/kg)。依托泊苷的剂量如前所述使寿命延长了175%。腹腔注射后10分钟内DNA发生链断裂,但随着注射与从小鼠体内取出细胞之间的时间间隔延长至1小时和3小时,观察到DNA的持续修复。注射后6小时,DNA的最大浓度接近对照浓度。在我们之前的研究中,阿糖胞苷在依托泊苷给药后3至6小时给予时最有效。对阿糖胞苷的敏感性可能在依托泊苷诱导的DNA损伤修复期间增加。所有四种脱氧核苷三磷酸(dNTP)在6小时内逐渐增加,最高可达对照的3倍。核糖核苷三磷酸(rNTP)的变化相似,但变化程度小于dNTP。dNTP和rNTP的这些变化将是决定依托泊苷与核苷类似物联合抗肿瘤效果的一个重要因素。

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