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鸟氨酸脱羧酶竞争性抑制剂α-甲基鸟氨酸对艾氏腹水瘤细胞的体内杀细胞作用。

Cytocidal effect of alpha-methylornithine, a competitive inhibitor of ornithine decarboxylase, on ehrlich ascites tumor cells in vivo.

作者信息

Linden M, Oredsson S, Heby O

出版信息

Cancer Lett. 1980 May;9(3):207-12. doi: 10.1016/0304-3835(80)90088-9.

Abstract

The antiproliferative effect of alpha-methylornithine, an inhibitor of the initial and rate-limiting step in polyamine biosynthesis, was studied on Ehrlich ascites tumor cells grown in vivo. To assess drug-induced cell lethality, the loss of 125I from mice harboring 5-[125I] iodo-2'-deoxyuridine-labeled mouse tumor cells was determined during the course of alpha-methylornithine treatment. Mice that received the drug showed a significant increase in their rate of 125I excretion as compared to controls. This suggests that alpha-methylornithine kills an additional fraction of tumor cells beyond the fraction normally dying.

摘要

研究了α-甲基鸟氨酸(一种多胺生物合成起始限速步骤的抑制剂)对体内生长的艾氏腹水瘤细胞的抗增殖作用。为评估药物诱导的细胞致死率,在α-甲基鸟氨酸治疗过程中,测定了携带5-[¹²⁵I]碘-2'-脱氧尿苷标记的小鼠肿瘤细胞的小鼠¹²⁵I的流失情况。与对照组相比,接受药物治疗的小鼠¹²⁵I排泄率显著增加。这表明,α-甲基鸟氨酸除了能杀死正常死亡的肿瘤细胞部分外,还能杀死额外一部分肿瘤细胞。

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