Overproduction of ornithine decarboxylase caused by relief of translational repression is associated with neoplastic transformation

• Published in: Cancer research (Chicago, Ill.) Ill.), 1994-05, Vol.54 (9), p.2313-2316
• Main Authors: SHANTZ, L. M, PEGG, A. E
• Format: Article
• Language: English
• Subjects: 3T3 Cells; Adenosylmethionine Decarboxylase - biosynthesis; Adenosylmethionine Decarboxylase - genetics; Animals; Base Sequence; Biological and medical sciences; Cell physiology; Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes; Eflornithine - pharmacology; Eukaryotic Initiation Factor-4E; Fundamental and applied biological sciences. Psychology; Luciferases - metabolism; Mice; Molecular and cellular biology; Molecular Sequence Data; Open Reading Frames; Ornithine Decarboxylase - biosynthesis; Ornithine Decarboxylase - genetics; Peptide Initiation Factors - biosynthesis; Protein Biosynthesis - drug effects; RNA, Messenger - biosynthesis; Time Factors
• ISSN: 0008-5472; 1538-7445

The mRNAs for two key enzymes in polyamine biosynthesis, ornithine decarboxylase (ODC) and S-adenosylmethionine decarboxylase (AdoMetDC), both long 5' untranslated regions (5'UTRs) that could be important in the regulation of enzyme levels by affecting the translation of these mRNAs. In order to test this hypothesis, ODC and AdoMetDC activities were measured in 3T3 cells and in 3T3 cells overexpressing eIF-4E (P2 cells). eIF-4E has been reported to be a limiting factor in the translation of mRNAs with extensive secondary structures in the 5'UTR. AdoMetDC activity was not greatly different in the two cell lines, but ODC activity was much greater in the P2 cells. These results were confirmed by transfecting these cells with plasmids containing a luciferase complementary DNA fused to follow the 5'UTR from ODC or AdoMetDC. The ODC 5'UTR construct produced a higher luciferase activity in the P2 cells. The high level of expression of ODC may be a critical factor in the transformed phenotype of the P2 cells since the ability of these cells to grow in soft agar was blocked by levels of the ODC inhibitor, alpha-difluoromethylornithine, that reduced the ODC activity to values comparable to those of the parent 3T3 cells. These results provide more evidence for a critical role of ODC activity in neoplastic transformation and for the importance of its translational regulation in cell growth and transformation.