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Effects of resveratrol and other wine polyphenols on the proliferation, apoptosis and androgen receptor expression in LNCaP cells.

Authors :
Ferruelo A
Romero I
Cabrera PM
Arance I
Andrés G
Angulo JC
Source :
Actas urologicas espanolas [Actas Urol Esp] 2014 Jul-Aug; Vol. 38 (6), pp. 397-404. Date of Electronic Publication: 2014 Apr 13.
Publication Year :
2014

Abstract

Purpose: To address the effect of resveratrol and other red wine polyphenols on cell proliferation, apoptosis and androgen receptor (AR) expression in human prostate cancer LNCaP cells.<br />Materials and Methods: LNCaP cells (5 × 102) were cultured in microtiter plate modules and treated with gallic acid, tannic acid and quercetin (1, 5 and 10 μM), rutin and morin (25, 50 and 75 μM) and resveratrol (5, 10 and 25 μM). To address the extent of proliferation at 24, 48, 72 and 96 hours, a colorimetric immunoassay method was used. An activity caspase 3/7 detection assay was used to disclose apoptosis at 24, 48 and 72 hours. AR mARN levels were determined by real time RT-PCR.<br />Results: All polyphenols studied significantly inhibited (P<.05) cell proliferation compared to control. However, there were moderate differences between them. Resveratrol was the strongest inhibitor at different times and doses. Also, caspase-3 and caspase-7 activity was significantly higher (P<.05) than control in the presence of all the compounds, but the earlier response was achieved by resveratrol. Resveratrol, quercetin and morin were the only nutrients that significantly inhibited AR mRNA expression. Again resveratrol produced the highest inhibition (90-250 times less than control), followed by morin (67-100 times) and quercetin (55-91 times).<br />Conclusions: All polyphenols studied showed important antiproliferative effects and induced apoptosis when added to LNCaP cells culture. We confirm that resveratrol, morin and quercetin may achieve such effect through reduced expression of AR. The synergistic effects of these compounds and their potential to prevent progression of hormone-dependent prostate cancer merit further study.<br /> (Copyright © 2014 AEU. Published by Elsevier Espana. All rights reserved.)

Details

Language :
English; Spanish; Castilian
ISSN :
1699-7980
Volume :
38
Issue :
6
Database :
MEDLINE
Journal :
Actas urologicas espanolas
Publication Type :
Academic Journal
Accession number :
24726691
Full Text :
https://doi.org/10.1016/j.acuro.2014.02.012