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在经马磷酰胺处理后发生凋亡的HL-60细胞中,C-myc表达下调。

C-myc expression is down-regulated in mafosfamide-treated HL-60 cells undergoing apoptosis.

作者信息

Davidoff A N, Mendelow B V

机构信息

Department of Haematology, School of Pathology, University of the Witwatersrand, Parktown, South Africa.

出版信息

Anticancer Res. 1993 Jul-Aug;13(4):1167-70.

PMID:8352540
Abstract

The expression of the proto-oncogene c-myc has been strongly implicated in the regulation of apoptosis. Since we have previously shown apoptosis to occur in HL-60 leukemic cells exposed to the prodrug Mafosfamide (ASTA Z 7557), the present study was undertaken to examine the levels of c-myc mRNA transcripts in such cells. Mafosfamide, which is a cyclophosphamide derivative that rapidly generates 4-Hydroperoxycyclophosphamide after aqueous dissolution, was employed in doses ranging from 0.1 to 20 micrograms/ml. No changes in c-myc mRNA levels were evident after 1 hour of exposure to Mafosfamide. After 6 and 24 hours of Mafosfamide-exposure, however, there was a dose- and time-dependent decrease in c-myc transcripts. c-myc mRNA expression was reduced to a greater extent than was either beta-actin of GAPDH expression. Morphological, biochemical and ultrastructural evidence of apoptosis accompanied the Mafosfamide-induced c-myc mRNA down-regulation at 24 hours. We conclude that, in the context of Mafosfamide-treated HL-60 cells, upregulation of c-myc mRNA transcription was not fundamental for the activation of the apoptotic cascade.

摘要

原癌基因c-myc的表达与细胞凋亡的调控密切相关。由于我们之前已表明,暴露于前体药物马磷酰胺(ASTA Z 7557)的HL-60白血病细胞会发生凋亡,因此本研究旨在检测此类细胞中c-myc mRNA转录本的水平。马磷酰胺是一种环磷酰胺衍生物,在水溶液溶解后能迅速生成4-氢过氧环磷酰胺,使用剂量范围为0.1至20微克/毫升。暴露于马磷酰胺1小时后,c-myc mRNA水平无明显变化。然而,在暴露于马磷酰胺6小时和24小时后,c-myc转录本出现了剂量和时间依赖性下降。c-myc mRNA表达的降低程度大于β-肌动蛋白或甘油醛-3-磷酸脱氢酶(GAPDH)表达的降低程度。24小时时,凋亡的形态学、生化和超微结构证据伴随着马磷酰胺诱导的c-myc mRNA下调。我们得出结论,在马磷酰胺处理的HL-60细胞中,c-myc mRNA转录上调并非凋亡级联激活的根本原因。

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