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原癌基因c-myc和c-fos被c-ras激活:多胺的参与。

Activation of the proto-oncogene c-myc and c-fos by c-ras: involvement of polyamines.

作者信息

Tabib A, Bachrach U

机构信息

Department of Molecular Biology, Hebrew University, Hadassah Medical School, Jerusalem, Israel.

出版信息

Biochem Biophys Res Commun. 1994 Jul 29;202(2):720-7. doi: 10.1006/bbrc.1994.1990.

Abstract

Rat kidney cells infected with a temperature-sensitive mutant of Kirsten sarcoma virus (Ki-MSV ts 371) expressed Ki-Ras at 37 degrees C but not at 42 degrees C. This expression of the oncogene was accompanied by an increase in the activity of ornithine decarboxylase (ODC) and the accumulation of putrescine. Elevation of cellular polyamine content triggered the transcription of c-myc and c-fos. alpha-Difluoromethylornithine, a specific inhibitor of ODC, prevented the transcription of c-myc in cells grown at 37 degrees C. Putrescine, at physiological concentrations, triggered the transcription of c-myc and c-fos in cells grown at 42 degrees C, when Ki-ras was not expressed. It has been suggested that polyamines participate in a cascade of events leading to the communication between membrane-bound and nuclear oncogene products. These findings may attribute a new function to the naturally occurring polyamines.

摘要

感染了柯斯顿肉瘤病毒温度敏感突变体(Ki-MSV ts 371)的大鼠肾细胞在37℃时表达Ki-Ras,而在42℃时不表达。癌基因的这种表达伴随着鸟氨酸脱羧酶(ODC)活性的增加和腐胺的积累。细胞内多胺含量的升高触发了c-myc和c-fos的转录。α-二氟甲基鸟氨酸是ODC的特异性抑制剂,可阻止在37℃生长的细胞中c-myc的转录。在生理浓度下,腐胺在42℃生长的细胞中触发了c-myc和c-fos的转录,此时Ki-ras不表达。有人提出,多胺参与了一系列导致膜结合癌基因产物与核癌基因产物之间通讯的事件。这些发现可能赋予天然存在的多胺一种新功能。

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