Cargando…

Celastrol inhibits gastric cancer growth by induction of apoptosis and autophagy

Recently, the interest in natural products for the treatment of cancer is increasing because they are the pre-screened candidates. In the present study, we demonstrate the therapeutic effect of celastrol, a triterpene extracted from the root bark of Chinese medicine on gastric cancer. The proliferat...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Hyun-Woo, Jang, Kenny Seung Bin, Choi, Hye Ji, Jo, Ara, Cheong, Jae-Ho, Chun, Kyung-Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345515/
https://www.ncbi.nlm.nih.gov/pubmed/24667175
http://dx.doi.org/10.5483/BMBRep.2014.47.12.069
_version_ 1782359587094003712
author Lee, Hyun-Woo
Jang, Kenny Seung Bin
Choi, Hye Ji
Jo, Ara
Cheong, Jae-Ho
Chun, Kyung-Hee
author_facet Lee, Hyun-Woo
Jang, Kenny Seung Bin
Choi, Hye Ji
Jo, Ara
Cheong, Jae-Ho
Chun, Kyung-Hee
author_sort Lee, Hyun-Woo
collection PubMed
description Recently, the interest in natural products for the treatment of cancer is increasing because they are the pre-screened candidates. In the present study, we demonstrate the therapeutic effect of celastrol, a triterpene extracted from the root bark of Chinese medicine on gastric cancer. The proliferation of AGS and YCC-2 cells were most sensitively decreased in six kinds of gastric cancer cell lines after the treatment with celastrol. Celastrol inhibited the cell migration and increased G1 arrest in cell-cycle populations in both cell lines. The treatment with celastrol significantly induced autophagy and apoptosis and increased the expression of autophagy and apoptosis-related proteins. We also found an increase in phosphorylated AMPK following a decrease in all phosphorylated forms of AKT, mTOR and S6K after the treatment with celastrol. Moreover, gastric tumor burdens were reduced in a dose-dependent manner by celastrol administration in a xenografted mice model. Taken together, celastrol distinctly inhibits the gastric cancer cell proliferation and induces autophagy and apoptosis. [BMB Reports 2014; 47(12): 697-702]
format Online
Article
Text
id pubmed-4345515
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Korean Society for Biochemistry and Molecular Biology
record_format MEDLINE/PubMed
spelling pubmed-43455152015-03-02 Celastrol inhibits gastric cancer growth by induction of apoptosis and autophagy Lee, Hyun-Woo Jang, Kenny Seung Bin Choi, Hye Ji Jo, Ara Cheong, Jae-Ho Chun, Kyung-Hee BMB Rep Research-Articles Recently, the interest in natural products for the treatment of cancer is increasing because they are the pre-screened candidates. In the present study, we demonstrate the therapeutic effect of celastrol, a triterpene extracted from the root bark of Chinese medicine on gastric cancer. The proliferation of AGS and YCC-2 cells were most sensitively decreased in six kinds of gastric cancer cell lines after the treatment with celastrol. Celastrol inhibited the cell migration and increased G1 arrest in cell-cycle populations in both cell lines. The treatment with celastrol significantly induced autophagy and apoptosis and increased the expression of autophagy and apoptosis-related proteins. We also found an increase in phosphorylated AMPK following a decrease in all phosphorylated forms of AKT, mTOR and S6K after the treatment with celastrol. Moreover, gastric tumor burdens were reduced in a dose-dependent manner by celastrol administration in a xenografted mice model. Taken together, celastrol distinctly inhibits the gastric cancer cell proliferation and induces autophagy and apoptosis. [BMB Reports 2014; 47(12): 697-702] Korean Society for Biochemistry and Molecular Biology 2014-12 /pmc/articles/PMC4345515/ /pubmed/24667175 http://dx.doi.org/10.5483/BMBRep.2014.47.12.069 Text en Copyright © 2014, Korean Society for Biochemistry and Molecular Biology 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 Research-Articles
Lee, Hyun-Woo
Jang, Kenny Seung Bin
Choi, Hye Ji
Jo, Ara
Cheong, Jae-Ho
Chun, Kyung-Hee
Celastrol inhibits gastric cancer growth by induction of apoptosis and autophagy
title Celastrol inhibits gastric cancer growth by induction of apoptosis and autophagy
title_full Celastrol inhibits gastric cancer growth by induction of apoptosis and autophagy
title_fullStr Celastrol inhibits gastric cancer growth by induction of apoptosis and autophagy
title_full_unstemmed Celastrol inhibits gastric cancer growth by induction of apoptosis and autophagy
title_short Celastrol inhibits gastric cancer growth by induction of apoptosis and autophagy
title_sort celastrol inhibits gastric cancer growth by induction of apoptosis and autophagy
topic Research-Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345515/
https://www.ncbi.nlm.nih.gov/pubmed/24667175
http://dx.doi.org/10.5483/BMBRep.2014.47.12.069
work_keys_str_mv AT leehyunwoo celastrolinhibitsgastriccancergrowthbyinductionofapoptosisandautophagy
AT jangkennyseungbin celastrolinhibitsgastriccancergrowthbyinductionofapoptosisandautophagy
AT choihyeji celastrolinhibitsgastriccancergrowthbyinductionofapoptosisandautophagy
AT joara celastrolinhibitsgastriccancergrowthbyinductionofapoptosisandautophagy
AT cheongjaeho celastrolinhibitsgastriccancergrowthbyinductionofapoptosisandautophagy
AT chunkyunghee celastrolinhibitsgastriccancergrowthbyinductionofapoptosisandautophagy