An evaluation of the anti-neoplastic activity of curcumin in prostate cancer cell lines

OBJECTIVE: The aim of our study is to investigate the anti-neoplastic effect of curcumin in prostate cancer cell lines. Specifically, we are using the LNCaP cell line and another prostate cell line developed in our laboratory, PcBra1. The PcBra1 cells were derived from a localized, obstructive prost...

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Main Authors: Camila B. Piantino, Fernanda A. Salvadori, Pedro P. Ayres, Raphael B. Kato, Victor Srougi, Katia R. Leite, Miguel Srougi
Format: Article
Language:English
Published: Sociedade Brasileira de Urologia 2009-06-01
Series:International Brazilian Journal of Urology
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382009000300012
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author Camila B. Piantino
Fernanda A. Salvadori
Pedro P. Ayres
Raphael B. Kato
Victor Srougi
Katia R. Leite
Miguel Srougi
author_facet Camila B. Piantino
Fernanda A. Salvadori
Pedro P. Ayres
Raphael B. Kato
Victor Srougi
Katia R. Leite
Miguel Srougi
author_sort Camila B. Piantino
collection DOAJ
description OBJECTIVE: The aim of our study is to investigate the anti-neoplastic effect of curcumin in prostate cancer cell lines. Specifically, we are using the LNCaP cell line and another prostate cell line developed in our laboratory, PcBra1. The PcBra1 cells were derived from a localized, obstructive prostate cancer with a Gleason score of 9 (4+5). MATERIAL AND METHODS: A prostate cancer cell line was isolated from a localized, obstructive prostate cancer with a Gleason score of 9 (4+5), and it was characterized using immunohistochemistry. After six passages, the new cell line was treated with varying doses of curcumin: 10 µM, 25 µM or 50 µM. Apoptosis was detected by flow cytometry using Annexin V FITC. For comparison, the same experiment was performed using the well-established metastatic prostate cancer cell line, LNCaP. RESULTS: Increasing concentrations of curcumin promoted more apoptosis in the PcBra1 cells. Exposure to 10 and 25 µM curcumin induced apoptosis in 31.9% and 52.2% of cells, respectively. Late apoptosis was induced in 37% of cells after treatment with 10 µM curcumin and 35% of cells with a 25 µM treatment. Necrosis accounted for less than 10% of the death in these cells at those two concentrations. When curcumin was used at 50 µM, apoptosis was observed in 64.3% of the cells. Including late apoptosis and necrosis, 98.6% of the cells died in response to 50 µM curcumin. Results with the LNCaP cells were similar although late apoptosis was the main phenomenon at 25 µM. CONCLUSION: We have shown that curcumin acts on localized prostate cancer to induce apoptosis and may therefore be an option as a future therapeutic agent.
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spelling doaj.art-9948efb3327d49bcae2b76ee5b2368132022-12-22T02:33:34ZengSociedade Brasileira de UrologiaInternational Brazilian Journal of Urology1677-55381677-61192009-06-0135335436110.1590/S1677-55382009000300012An evaluation of the anti-neoplastic activity of curcumin in prostate cancer cell linesCamila B. PiantinoFernanda A. SalvadoriPedro P. AyresRaphael B. KatoVictor SrougiKatia R. LeiteMiguel SrougiOBJECTIVE: The aim of our study is to investigate the anti-neoplastic effect of curcumin in prostate cancer cell lines. Specifically, we are using the LNCaP cell line and another prostate cell line developed in our laboratory, PcBra1. The PcBra1 cells were derived from a localized, obstructive prostate cancer with a Gleason score of 9 (4+5). MATERIAL AND METHODS: A prostate cancer cell line was isolated from a localized, obstructive prostate cancer with a Gleason score of 9 (4+5), and it was characterized using immunohistochemistry. After six passages, the new cell line was treated with varying doses of curcumin: 10 µM, 25 µM or 50 µM. Apoptosis was detected by flow cytometry using Annexin V FITC. For comparison, the same experiment was performed using the well-established metastatic prostate cancer cell line, LNCaP. RESULTS: Increasing concentrations of curcumin promoted more apoptosis in the PcBra1 cells. Exposure to 10 and 25 µM curcumin induced apoptosis in 31.9% and 52.2% of cells, respectively. Late apoptosis was induced in 37% of cells after treatment with 10 µM curcumin and 35% of cells with a 25 µM treatment. Necrosis accounted for less than 10% of the death in these cells at those two concentrations. When curcumin was used at 50 µM, apoptosis was observed in 64.3% of the cells. Including late apoptosis and necrosis, 98.6% of the cells died in response to 50 µM curcumin. Results with the LNCaP cells were similar although late apoptosis was the main phenomenon at 25 µM. CONCLUSION: We have shown that curcumin acts on localized prostate cancer to induce apoptosis and may therefore be an option as a future therapeutic agent.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382009000300012curcumincurcuma longaprostate cancerapoptosis
spellingShingle Camila B. Piantino
Fernanda A. Salvadori
Pedro P. Ayres
Raphael B. Kato
Victor Srougi
Katia R. Leite
Miguel Srougi
An evaluation of the anti-neoplastic activity of curcumin in prostate cancer cell lines
International Brazilian Journal of Urology
curcumin
curcuma longa
prostate cancer
apoptosis
title An evaluation of the anti-neoplastic activity of curcumin in prostate cancer cell lines
title_full An evaluation of the anti-neoplastic activity of curcumin in prostate cancer cell lines
title_fullStr An evaluation of the anti-neoplastic activity of curcumin in prostate cancer cell lines
title_full_unstemmed An evaluation of the anti-neoplastic activity of curcumin in prostate cancer cell lines
title_short An evaluation of the anti-neoplastic activity of curcumin in prostate cancer cell lines
title_sort evaluation of the anti neoplastic activity of curcumin in prostate cancer cell lines
topic curcumin
curcuma longa
prostate cancer
apoptosis
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382009000300012
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