Inhibition of proto-oncogene c-fos transcription by inhibitors of protein kinase C and ion transport.

Inhibition of proto-oncogene c-fos transcription by inhibitors of protein kinase C and ion transport.
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蛋白激酶 C 和离子转运抑制剂抑制原癌基因 c-fos 转录。

DOI:
10.1111/j.1432-1033.1987.tb10985.x
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发表时间:
1987
期刊:
European journal of biochemistry
影响因子:
--
通讯作者:
K. Nose
K. Nose
中科院分区:
--
文献类型:
--
作者:
M. Shibanuma;T. Kuroki;K. Nose

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Both 4 beta-phorbol 12,13-didecanoate (PDD) and calcium ionophore A23187 induced c-fos mRNA accumulation with similar kinetics in human monocyte-like cells (U937). Their effects were additive. Cells pretreated with PDD were not induced to accumulate c-fos mRNA by PDD but remained responsive to the induction by A23187. Similarly cells pretreated with A23187 responded to PDD but not to A23187. Nuclear run-off transcription assay indicated that increase in the c-fos mRNA level after the second inducer treatment corresponded to transcriptional activation of the c-fos gene. The accumulation of c-fos mRNA and the transcriptional activation of c-fos induced by PDD or A23187 were inhibited by the protein kinase inhibitor H-7 and by quinidine and amiloride. The induction by A23187, but not that by PDD, was also inhibited by 4-aminopyridine, or tetraethylammonium. From these results, it is proposed that activation of protein kinase C and Na+ or K+ transport are required for c-fos induction caused by PDD and A23187.
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