Premium
Expression of spermidine/spermine N 1 ‐acetyltransferase in growing Yoshida AH‐130 hepatoma cells
Author(s) -
Desiderio Maria Alfonsina,
Bardella Lidia
Publication year - 1994
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.1840190327
Subject(s) - spermidine , spermine , putrescine , polyamine , polyamine oxidase , biology , enzyme , in vitro , ornithine decarboxylase , acetyltransferase , microbiology and biotechnology , cell growth , biochemistry , medicine , endocrinology , acetylation , gene
Activity and messenger RNA levels of spermidine/spermine N 1 ‐acetyltransferase, the rate‐limiting enzyme of the polyamine interconversion pathway, were investigated in host liver and in Yoshida AH‐130 ascites hepatoma cells as a function of tumor growth phases. Enzyme activity reached maximal values at day 10 in host liver (2.0‐fold increase) and at days 10 and 14 in hepatoma cells (4.2‐ and 5.4‐fold increases)– that is, when the cellular growth was nearly arrested. At day 10 the messenger RNA levels of spermidine/spermine N 1 ‐acetyltransferase were augmented concomitantly; they were about two and four times higher, respectively, in host liver and tumor cells than in control liver. The in vitro transcription rate seemed to be constant during hepatoma cell growth. Treatment of the animals with N 1 , N 2 ‐ bis ‐(2,3‐butadienyl)‐1,4‐butanediamine (MDL 72527), a specific inhibitor of polyamine oxidase, caused large accumulation of N 1 ‐acetylspermidine in hepatoma cells and in the ascitic fluid; the maximal values were reached at day 14. The levels of putrescine in inhibitor‐treated rats decreased in hepatoma cells (day 5) and in ascitic fluid (days 5 and 14), whereas values of spermidine and spermine remained unchanged. The proposed role for spermidine/spermine N 1 ‐acetyltransferase‐enhanced expression is to regulate the cellular polyamine pool by causing their excretion as acetylderivatives from tumor cells into the ascitic fluid, even if putrescine seems also to be excreted. Eventual repeat uptake of putrescine by hepatoma cells could contribute to the control of cellular polyamine levels. (Hepatology 1994;19:728–734).