Effect of polyamine analogues and inhibition of polyamine oxidase on spermidine/spermine N1-acetyltransferase activity and cell proliferation
Pegg, A.E.; Hu, R.H.
Cancer Letters 95(1-2): 247-252
1995
ISSN/ISBN: 0304-3835 PMID: 7656239 DOI: 10.1016/0304-3835(95)03897-6
Accession: 008542712
Several bis(ethyl)polyamine analogues are currently undergoing trials as antitumor agents. The ability of some of these analogues to induce spermidine/spermine NI-acetyltransferase and to inhibit cell proliferation was examined in a number of different cell lines. Although N-1, N-11 bis(ethyl)norspermine was a potent inducer of the acetylase in all cell lines tested, there was a striking difference in the acetylase induction in response to N,N'-bis(ethylamino)propyl)-1,7-heptanediamine. This was a very strong inducer in CHO cells but had no effect in HT29 cells and very little effect in COS-7 or L1210 cells. There was no correlation between the induction of the acetylase and the ability of these analogues to inhibit cell proliferation since N-1,N-11-bis(ethylamino)-propyl)-1,7-heptanediamine was as at least as strongly antiproliferative as N-1,N-11-bis(ethyl)-norspermine or N-1,N-12-bis(ethyl)spermine. Acetylase induction and the intracellular level of the analogues were increased in CHO cells by treatment with a polyamine oxidase inhibitor suggesting that they are degraded by polyamine oxidase. The absence of polyamine oxidase in some tumors may therefore contribute to their sensitivity to these analogues.