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Anticancer effect of tectochrysin in colon cancer cell via suppression of NF-kappaB activity and enhancement of death receptor expression

BACKGROUND: Flavonoids are a diverse family of natural phenolic compounds commonly found in fruits and vegetables. Epidemiologic studies showed that flavonoids also reduce the risk of colon cancer. Tectochrysin is one of the major flavonoids of Alpinia oxyphylla Miquel. However, the anti-cancer effe...

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Autores principales: Park, Mi Hee, Hong, Ji Eun, Park, Eun Sook, Yoon, Hee Sung, Seo, Doo Won, Hyun, Byung Kook, Han, Sang-Bae, Ham, Young Won, Hwang, Bang Yeon, Hong, Jin Tae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487202/
https://www.ncbi.nlm.nih.gov/pubmed/26123287
http://dx.doi.org/10.1186/s12943-015-0377-2
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author Park, Mi Hee
Hong, Ji Eun
Park, Eun Sook
Yoon, Hee Sung
Seo, Doo Won
Hyun, Byung Kook
Han, Sang-Bae
Ham, Young Won
Hwang, Bang Yeon
Hong, Jin Tae
author_facet Park, Mi Hee
Hong, Ji Eun
Park, Eun Sook
Yoon, Hee Sung
Seo, Doo Won
Hyun, Byung Kook
Han, Sang-Bae
Ham, Young Won
Hwang, Bang Yeon
Hong, Jin Tae
author_sort Park, Mi Hee
collection PubMed
description BACKGROUND: Flavonoids are a diverse family of natural phenolic compounds commonly found in fruits and vegetables. Epidemiologic studies showed that flavonoids also reduce the risk of colon cancer. Tectochrysin is one of the major flavonoids of Alpinia oxyphylla Miquel. However, the anti-cancer effects and the molecular mechanisms of tectochrysin in colon cancer cells have not yet been reported. We investigated whether tectochrysin could inhibit colon cancer cell growth at 1, 5, 10 μg/ml. In in vivo study, we injected a tectochrysin treatment dose of 5 mg/kg to each mouse. RESULTS: Tectochrysin suppressed the growth of SW480 and HCT116 human colon cancer cells. The expression of DR3, DR4 and Fas were significantly increased, and pro-apoptotic proteins were also increased. Tectochrysin treatment also inhibited activity of NF-κB. A docking model indicated that tectochrysin binds directly to the p50 unit. In in vivo, tumor weights and volumes in mice were reduced when treated with tectochrysin. Tectochrysin leads to apoptotic cell death in colon cancer cells through activation of death receptors expression via the inhibition of NF-κB. CONCLUSIONS: Tectochrysin can be a useful agent for the treatment of colon cancer cell growth as well as an adjuvant agent for chemo-resistant cancer cells growth.
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spelling pubmed-44872022015-07-02 Anticancer effect of tectochrysin in colon cancer cell via suppression of NF-kappaB activity and enhancement of death receptor expression Park, Mi Hee Hong, Ji Eun Park, Eun Sook Yoon, Hee Sung Seo, Doo Won Hyun, Byung Kook Han, Sang-Bae Ham, Young Won Hwang, Bang Yeon Hong, Jin Tae Mol Cancer Research BACKGROUND: Flavonoids are a diverse family of natural phenolic compounds commonly found in fruits and vegetables. Epidemiologic studies showed that flavonoids also reduce the risk of colon cancer. Tectochrysin is one of the major flavonoids of Alpinia oxyphylla Miquel. However, the anti-cancer effects and the molecular mechanisms of tectochrysin in colon cancer cells have not yet been reported. We investigated whether tectochrysin could inhibit colon cancer cell growth at 1, 5, 10 μg/ml. In in vivo study, we injected a tectochrysin treatment dose of 5 mg/kg to each mouse. RESULTS: Tectochrysin suppressed the growth of SW480 and HCT116 human colon cancer cells. The expression of DR3, DR4 and Fas were significantly increased, and pro-apoptotic proteins were also increased. Tectochrysin treatment also inhibited activity of NF-κB. A docking model indicated that tectochrysin binds directly to the p50 unit. In in vivo, tumor weights and volumes in mice were reduced when treated with tectochrysin. Tectochrysin leads to apoptotic cell death in colon cancer cells through activation of death receptors expression via the inhibition of NF-κB. CONCLUSIONS: Tectochrysin can be a useful agent for the treatment of colon cancer cell growth as well as an adjuvant agent for chemo-resistant cancer cells growth. BioMed Central 2015-06-30 /pmc/articles/PMC4487202/ /pubmed/26123287 http://dx.doi.org/10.1186/s12943-015-0377-2 Text en © Park et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Park, Mi Hee
Hong, Ji Eun
Park, Eun Sook
Yoon, Hee Sung
Seo, Doo Won
Hyun, Byung Kook
Han, Sang-Bae
Ham, Young Won
Hwang, Bang Yeon
Hong, Jin Tae
Anticancer effect of tectochrysin in colon cancer cell via suppression of NF-kappaB activity and enhancement of death receptor expression
title Anticancer effect of tectochrysin in colon cancer cell via suppression of NF-kappaB activity and enhancement of death receptor expression
title_full Anticancer effect of tectochrysin in colon cancer cell via suppression of NF-kappaB activity and enhancement of death receptor expression
title_fullStr Anticancer effect of tectochrysin in colon cancer cell via suppression of NF-kappaB activity and enhancement of death receptor expression
title_full_unstemmed Anticancer effect of tectochrysin in colon cancer cell via suppression of NF-kappaB activity and enhancement of death receptor expression
title_short Anticancer effect of tectochrysin in colon cancer cell via suppression of NF-kappaB activity and enhancement of death receptor expression
title_sort anticancer effect of tectochrysin in colon cancer cell via suppression of nf-kappab activity and enhancement of death receptor expression
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487202/
https://www.ncbi.nlm.nih.gov/pubmed/26123287
http://dx.doi.org/10.1186/s12943-015-0377-2
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