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Anti-carcinogenic effects of non-polar components containing licochalcone A in roasted licorice root

BACKGROUND/OBJECTIVE: Licorice has been shown to possess cancer chemopreventive effects. However, glycyrrhizin, a major component in licorice, was found to interfere with steroid metabolism and cause edema and hypertension. The roasting process of licorice modifies the chemical composition and conve...

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Autores principales: Park, So Young, Kim, Eun Ji, Choi, Hyun Ju, Seon, Mi Ra, Lim, Soon Sung, Kang, Young-Hee, Choi, Myung-Sook, Lee, Ki Won, Yoon Park, Jung Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Nutrition Society and the Korean Society of Community Nutrition 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058558/
https://www.ncbi.nlm.nih.gov/pubmed/24944769
http://dx.doi.org/10.4162/nrp.2014.8.3.257
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author Park, So Young
Kim, Eun Ji
Choi, Hyun Ju
Seon, Mi Ra
Lim, Soon Sung
Kang, Young-Hee
Choi, Myung-Sook
Lee, Ki Won
Yoon Park, Jung Han
author_facet Park, So Young
Kim, Eun Ji
Choi, Hyun Ju
Seon, Mi Ra
Lim, Soon Sung
Kang, Young-Hee
Choi, Myung-Sook
Lee, Ki Won
Yoon Park, Jung Han
author_sort Park, So Young
collection PubMed
description BACKGROUND/OBJECTIVE: Licorice has been shown to possess cancer chemopreventive effects. However, glycyrrhizin, a major component in licorice, was found to interfere with steroid metabolism and cause edema and hypertension. The roasting process of licorice modifies the chemical composition and converts glycyrrhizin to glycyrrhetinic acid. The purpose of this study was to examine the anti-carcinogenic effects of the ethanol extract of roasted licorice (EERL) and to identify the active compound in EERL. MATERIALS/METHODS: Ethanol and aqueous extracts of roasted and un-roasted licorice were prepared. The active fraction was separated from the methylene chloride (MC)-soluble fraction of EERL and the structure of the purified compound was determined by nuclear magnetic resonance spectroscopy. The anti-carcinogenic effects of licorice extracts and licochalcone A was evaluated using a MTT assay, Western blot, flow cytometry, and two-stage skin carcinogenesis model. RESULTS: EERL was determined to be more potent and efficacious than the ethanol extract of un-roasted licorice in inhibiting the growth of DU145 and MLL prostate cancer cells, as well as HT-29 colon cancer cells. The aqueous extracts of un-roasted and roasted licorice showed minimal effects on cell growth. EERL potently inhibited growth of MCF-7 and MDA-MB-231 breast, B16-F10 melanoma, and A375 and A2058 skin cancer cells, whereas EERL slightly stimulated the growth of normal IEC-6 intestinal epithelial cells and CCD118SK fibroblasts. The MC-soluble fraction was more efficacious than EERL in inhibiting DU145 cell growth. Licochalcone A was isolated from the MC fraction and identified as the active compound of EERL. Both EERL and licochalcone A induced apoptosis of DU145 cells. EERL potently inhibited chemically-induced skin papilloma formation in mice. CONCLUSIONS: Non-polar compounds in EERL exert potent anti-carcinogenic effects, and that roasted rather than un-roasted licorice should be favored as a cancer preventive agent, whether being used as an additive to food or medicine preparations.
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spelling pubmed-40585582014-06-18 Anti-carcinogenic effects of non-polar components containing licochalcone A in roasted licorice root Park, So Young Kim, Eun Ji Choi, Hyun Ju Seon, Mi Ra Lim, Soon Sung Kang, Young-Hee Choi, Myung-Sook Lee, Ki Won Yoon Park, Jung Han Nutr Res Pract Original Research BACKGROUND/OBJECTIVE: Licorice has been shown to possess cancer chemopreventive effects. However, glycyrrhizin, a major component in licorice, was found to interfere with steroid metabolism and cause edema and hypertension. The roasting process of licorice modifies the chemical composition and converts glycyrrhizin to glycyrrhetinic acid. The purpose of this study was to examine the anti-carcinogenic effects of the ethanol extract of roasted licorice (EERL) and to identify the active compound in EERL. MATERIALS/METHODS: Ethanol and aqueous extracts of roasted and un-roasted licorice were prepared. The active fraction was separated from the methylene chloride (MC)-soluble fraction of EERL and the structure of the purified compound was determined by nuclear magnetic resonance spectroscopy. The anti-carcinogenic effects of licorice extracts and licochalcone A was evaluated using a MTT assay, Western blot, flow cytometry, and two-stage skin carcinogenesis model. RESULTS: EERL was determined to be more potent and efficacious than the ethanol extract of un-roasted licorice in inhibiting the growth of DU145 and MLL prostate cancer cells, as well as HT-29 colon cancer cells. The aqueous extracts of un-roasted and roasted licorice showed minimal effects on cell growth. EERL potently inhibited growth of MCF-7 and MDA-MB-231 breast, B16-F10 melanoma, and A375 and A2058 skin cancer cells, whereas EERL slightly stimulated the growth of normal IEC-6 intestinal epithelial cells and CCD118SK fibroblasts. The MC-soluble fraction was more efficacious than EERL in inhibiting DU145 cell growth. Licochalcone A was isolated from the MC fraction and identified as the active compound of EERL. Both EERL and licochalcone A induced apoptosis of DU145 cells. EERL potently inhibited chemically-induced skin papilloma formation in mice. CONCLUSIONS: Non-polar compounds in EERL exert potent anti-carcinogenic effects, and that roasted rather than un-roasted licorice should be favored as a cancer preventive agent, whether being used as an additive to food or medicine preparations. The Korean Nutrition Society and the Korean Society of Community Nutrition 2014-06 2014-05-15 /pmc/articles/PMC4058558/ /pubmed/24944769 http://dx.doi.org/10.4162/nrp.2014.8.3.257 Text en ©2014 The Korean Nutrition Society and the Korean Society of Community Nutrition http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Park, So Young
Kim, Eun Ji
Choi, Hyun Ju
Seon, Mi Ra
Lim, Soon Sung
Kang, Young-Hee
Choi, Myung-Sook
Lee, Ki Won
Yoon Park, Jung Han
Anti-carcinogenic effects of non-polar components containing licochalcone A in roasted licorice root
title Anti-carcinogenic effects of non-polar components containing licochalcone A in roasted licorice root
title_full Anti-carcinogenic effects of non-polar components containing licochalcone A in roasted licorice root
title_fullStr Anti-carcinogenic effects of non-polar components containing licochalcone A in roasted licorice root
title_full_unstemmed Anti-carcinogenic effects of non-polar components containing licochalcone A in roasted licorice root
title_short Anti-carcinogenic effects of non-polar components containing licochalcone A in roasted licorice root
title_sort anti-carcinogenic effects of non-polar components containing licochalcone a in roasted licorice root
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058558/
https://www.ncbi.nlm.nih.gov/pubmed/24944769
http://dx.doi.org/10.4162/nrp.2014.8.3.257
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