Hurta R A
Department of Laboratory Medicine and Pathobiology, St. Michael's Hospital and the University of Toronto, Ontario, Canada.
Mol Cell Biochem. 2000 Dec;215(1-2):81-92. doi: 10.1023/a:1026539414863.
In the present study, the expression and the regulation of ornithine decarboxylase (ODC) and S-adenosylmethionine decarboxylase (SAMDC) was examined in a series of oncogene transformed cell lines. The expression of both ODC and SAMDC was found to correlate with the nature of the oncogene expressed and with the resulting cellular phenotype expressed. This study demonstrates, for the first time, that the expression of both ODC and SAMDC increases as a function of cellular transformation and, in particular, as a function of malignant progression. Ras transformed cells were shown to express a unique regulatory mechanism whereby a co-ordinate up-regulation of the expression of both ODC and SAMDC occurs (via post-transcriptional stabilization of their mRNA transcripts) in the presence of protein synthesis inhibition. Altered expression (and regulation) of both ODC and SAMDC is suggested to constitute an important part of an altered growth regulatory program inherent to oncogene transformed cells, in particular, to transformed cells capable of malignant progression.
在本研究中,对一系列癌基因转化细胞系中鸟氨酸脱羧酶(ODC)和S-腺苷甲硫氨酸脱羧酶(SAMDC)的表达及调控进行了检测。发现ODC和SAMDC的表达均与所表达癌基因的性质以及所产生的细胞表型相关。本研究首次证明,ODC和SAMDC的表达均随细胞转化而增加,特别是随恶性进展而增加。Ras转化细胞表现出一种独特的调控机制,即在存在蛋白质合成抑制的情况下,ODC和SAMDC的表达会协同上调(通过其mRNA转录本的转录后稳定)。ODC和SAMDC表达(及调控)的改变被认为是癌基因转化细胞固有生长调控程序改变的重要组成部分,特别是对于能够发生恶性进展的转化细胞而言。