Abstract |
7beta-OHsitosterol and 7beta-OHcholesterol are natural compounds of plant and animal cells with high structural similarity. Recently it was reported that both compounds induced apoptosis on human colon cancer cells by targeting different signalling pathways. Our study aimed at comparing their effects on polyamine metabolism and its relation to apoptosis. When human colon cancer cells were exposed to 7beta-OHsitosterol and to 7beta-OHcholesterol at concentrations inhibiting growth by the same degree, both compounds caused a reduction of polyamine biosynthetic enzyme activity, of the polyamine pools, and an increase of N1-acetylspermidine concentration indicating the enhancement of polyamine catabolism. Exogenous putrescine did not prevent cell death caused by 7beta-OHsitosterol, whereas 7beta-OHcholesterol-induced apoptosis was inhibited. MDL 72527, an inhibitor of polyamine oxidase, an enzyme of the polyamine catabolic pathway, potentiated the antiproliferative effects of 7beta-OHcholesterol by increasing the N1-acetylspermidine pool and enhanced the accumulation of apoptotic cells. In contrast, MDL 72527 did not change the apoptosis rate and the N1-acetylspermidine content in cells treated with 7beta-OHsitosterol. These data indicate that polyamine metabolic perturbations triggered by 7beta-OHcholesterol but not by 7beta-OHsitosterol are related to cell death.
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Authors | Stamatiki Roussi, Francine Gossé, Dalal Aoudé-Werner, Xin Zhang, Philippe Geoffroy, Michel Miesch, Eric Marchioni, Francis Raul |
Journal | International journal of oncology
(Int J Oncol)
Vol. 29
Issue 6
Pg. 1549-54
(Dec 2006)
ISSN: 1019-6439 [Print] Greece |
PMID | 17088995
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Biogenic Polyamines
- Hydroxycholesterols
- Sitosterols
- N(1)-acetylspermidine
- MDL 72527
- hydroxysitosterol
- cholest-5-en-3 beta,7 alpha-diol
- Spermidine
- Putrescine
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Topics |
- Biogenic Polyamines
(chemistry, metabolism)
- Caco-2 Cells
- Cell Death
(drug effects, physiology)
- Cell Growth Processes
(drug effects)
- Colonic Neoplasms
(drug therapy, metabolism, pathology)
- Drug Synergism
- Flow Cytometry
- Humans
- Hydroxycholesterols
(pharmacology)
- Putrescine
(analogs & derivatives, pharmacology)
- Sitosterols
(pharmacology)
- Spermidine
(analogs & derivatives, pharmacology)
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