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Anti-Cancer Effect of Lambertianic Acid by Inhibiting the AR in LNCaP Cells

Lambertianic acid (LA) is known to have anti-allergic and antibacterial effects. However, the anticancer activities and mechanism of action of LA have not been investigated. Therefore, the anticancer effects and mechanism of LA are investigated in this study. LA decreased not only AR protein levels,...

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Autores principales: Lee, Myoung-Sun, Lee, Seon-Ok, Kim, Sung-Hoon, Lee, Eun-Ok, Lee, Hyo-Jeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964442/
https://www.ncbi.nlm.nih.gov/pubmed/27399684
http://dx.doi.org/10.3390/ijms17071066
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author Lee, Myoung-Sun
Lee, Seon-Ok
Kim, Sung-Hoon
Lee, Eun-Ok
Lee, Hyo-Jeong
author_facet Lee, Myoung-Sun
Lee, Seon-Ok
Kim, Sung-Hoon
Lee, Eun-Ok
Lee, Hyo-Jeong
author_sort Lee, Myoung-Sun
collection PubMed
description Lambertianic acid (LA) is known to have anti-allergic and antibacterial effects. However, the anticancer activities and mechanism of action of LA have not been investigated. Therefore, the anticancer effects and mechanism of LA are investigated in this study. LA decreased not only AR protein levels, but also cellular and secretory levels of PSA. Furthermore, LA inhibited nuclear translocation of the AR induced by mibolerone. LA suppressed cell proliferation by inducing G(1) arrest, downregulating CDK4/6 and cyclin D1 and activating p53 and its downstream molecules, p21 and p27. LA induced apoptosis and the expression of related proteins, including cleaved caspase-9 and -3, c-PARP and BAX, and inhibited BCl-2. The role of AR in LA-induced apoptosis was assessed by using siRNA. Collectively, these findings suggest that LA exerts the anticancer effect by inhibiting AR and is a valuable therapeutic agent in prostate cancer treatment.
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spelling pubmed-49644422016-08-03 Anti-Cancer Effect of Lambertianic Acid by Inhibiting the AR in LNCaP Cells Lee, Myoung-Sun Lee, Seon-Ok Kim, Sung-Hoon Lee, Eun-Ok Lee, Hyo-Jeong Int J Mol Sci Article Lambertianic acid (LA) is known to have anti-allergic and antibacterial effects. However, the anticancer activities and mechanism of action of LA have not been investigated. Therefore, the anticancer effects and mechanism of LA are investigated in this study. LA decreased not only AR protein levels, but also cellular and secretory levels of PSA. Furthermore, LA inhibited nuclear translocation of the AR induced by mibolerone. LA suppressed cell proliferation by inducing G(1) arrest, downregulating CDK4/6 and cyclin D1 and activating p53 and its downstream molecules, p21 and p27. LA induced apoptosis and the expression of related proteins, including cleaved caspase-9 and -3, c-PARP and BAX, and inhibited BCl-2. The role of AR in LA-induced apoptosis was assessed by using siRNA. Collectively, these findings suggest that LA exerts the anticancer effect by inhibiting AR and is a valuable therapeutic agent in prostate cancer treatment. MDPI 2016-07-07 /pmc/articles/PMC4964442/ /pubmed/27399684 http://dx.doi.org/10.3390/ijms17071066 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lee, Myoung-Sun
Lee, Seon-Ok
Kim, Sung-Hoon
Lee, Eun-Ok
Lee, Hyo-Jeong
Anti-Cancer Effect of Lambertianic Acid by Inhibiting the AR in LNCaP Cells
title Anti-Cancer Effect of Lambertianic Acid by Inhibiting the AR in LNCaP Cells
title_full Anti-Cancer Effect of Lambertianic Acid by Inhibiting the AR in LNCaP Cells
title_fullStr Anti-Cancer Effect of Lambertianic Acid by Inhibiting the AR in LNCaP Cells
title_full_unstemmed Anti-Cancer Effect of Lambertianic Acid by Inhibiting the AR in LNCaP Cells
title_short Anti-Cancer Effect of Lambertianic Acid by Inhibiting the AR in LNCaP Cells
title_sort anti-cancer effect of lambertianic acid by inhibiting the ar in lncap cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964442/
https://www.ncbi.nlm.nih.gov/pubmed/27399684
http://dx.doi.org/10.3390/ijms17071066
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