Cargando…

Endoplasmic Reticulum Stress-Induced Resistance to Doxorubicin Is Reversed by Mulberry Leaf Polyphenol Extract in Hepatocellular Carcinoma through Inhibition of COX-2

Mulberry (Morus alba L.) leaves are used in Chinese medicine to treat metabolic disorders. Mulberry leaf polyphenol extracts (MLPE) have recently been shown to exhibit anticancer properties. Endoplasmic reticulum (ER) stress represents a pivotal obstacle in solid tumors, resulting in the antiapoptos...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Mon-Yuan, Wu, Cheng-Hsun, Hung, Tung-Wei, Wang, Chau-Jong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023226/
https://www.ncbi.nlm.nih.gov/pubmed/31888113
http://dx.doi.org/10.3390/antiox9010026
_version_ 1783498200908300288
author Yang, Mon-Yuan
Wu, Cheng-Hsun
Hung, Tung-Wei
Wang, Chau-Jong
author_facet Yang, Mon-Yuan
Wu, Cheng-Hsun
Hung, Tung-Wei
Wang, Chau-Jong
author_sort Yang, Mon-Yuan
collection PubMed
description Mulberry (Morus alba L.) leaves are used in Chinese medicine to treat metabolic disorders. Mulberry leaf polyphenol extracts (MLPE) have recently been shown to exhibit anticancer properties. Endoplasmic reticulum (ER) stress represents a pivotal obstacle in solid tumors, resulting in the antiapoptosis of tumor cells and drug resistance. In this study, pretreatment with the ER stress inducer tunicamycin (TM) attenuated the percentage of apoptosis induced by doxorubicin (DOX). Cotreatment with tunicamycin and MLPE reversed apoptosis induced by DOX. Simultaneously, induction of ER stress with tunicamycin resulted in an increased expression of Cyclooxygenase 2 (COX-2) and Glucose-regulated protein (GRP78) concomitant with the activation of p38 MAPK/PI3K/Akt in HepG2 cells. Furthermore, the suppression of ER stress with celecoxib or p38 MAPK inhibitor successfully recovered DOX-induced apoptosis. Consistent with the inhibition of COX-2 or p38 MAPK, copretreatment with TM and MLPE drastically recovered cytotoxicity and caspase-3 activation in the presence of DOX. These results reveal that MLPE reduces ER stress-induced resistance to DOX in hepatocellular carcinoma (HCC) cells through downregulation of COX-2- or p38 MAPK-mediated PI3K/Akt pathway.
format Online
Article
Text
id pubmed-7023226
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-70232262020-03-12 Endoplasmic Reticulum Stress-Induced Resistance to Doxorubicin Is Reversed by Mulberry Leaf Polyphenol Extract in Hepatocellular Carcinoma through Inhibition of COX-2 Yang, Mon-Yuan Wu, Cheng-Hsun Hung, Tung-Wei Wang, Chau-Jong Antioxidants (Basel) Article Mulberry (Morus alba L.) leaves are used in Chinese medicine to treat metabolic disorders. Mulberry leaf polyphenol extracts (MLPE) have recently been shown to exhibit anticancer properties. Endoplasmic reticulum (ER) stress represents a pivotal obstacle in solid tumors, resulting in the antiapoptosis of tumor cells and drug resistance. In this study, pretreatment with the ER stress inducer tunicamycin (TM) attenuated the percentage of apoptosis induced by doxorubicin (DOX). Cotreatment with tunicamycin and MLPE reversed apoptosis induced by DOX. Simultaneously, induction of ER stress with tunicamycin resulted in an increased expression of Cyclooxygenase 2 (COX-2) and Glucose-regulated protein (GRP78) concomitant with the activation of p38 MAPK/PI3K/Akt in HepG2 cells. Furthermore, the suppression of ER stress with celecoxib or p38 MAPK inhibitor successfully recovered DOX-induced apoptosis. Consistent with the inhibition of COX-2 or p38 MAPK, copretreatment with TM and MLPE drastically recovered cytotoxicity and caspase-3 activation in the presence of DOX. These results reveal that MLPE reduces ER stress-induced resistance to DOX in hepatocellular carcinoma (HCC) cells through downregulation of COX-2- or p38 MAPK-mediated PI3K/Akt pathway. MDPI 2019-12-26 /pmc/articles/PMC7023226/ /pubmed/31888113 http://dx.doi.org/10.3390/antiox9010026 Text en © 2019 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
Yang, Mon-Yuan
Wu, Cheng-Hsun
Hung, Tung-Wei
Wang, Chau-Jong
Endoplasmic Reticulum Stress-Induced Resistance to Doxorubicin Is Reversed by Mulberry Leaf Polyphenol Extract in Hepatocellular Carcinoma through Inhibition of COX-2
title Endoplasmic Reticulum Stress-Induced Resistance to Doxorubicin Is Reversed by Mulberry Leaf Polyphenol Extract in Hepatocellular Carcinoma through Inhibition of COX-2
title_full Endoplasmic Reticulum Stress-Induced Resistance to Doxorubicin Is Reversed by Mulberry Leaf Polyphenol Extract in Hepatocellular Carcinoma through Inhibition of COX-2
title_fullStr Endoplasmic Reticulum Stress-Induced Resistance to Doxorubicin Is Reversed by Mulberry Leaf Polyphenol Extract in Hepatocellular Carcinoma through Inhibition of COX-2
title_full_unstemmed Endoplasmic Reticulum Stress-Induced Resistance to Doxorubicin Is Reversed by Mulberry Leaf Polyphenol Extract in Hepatocellular Carcinoma through Inhibition of COX-2
title_short Endoplasmic Reticulum Stress-Induced Resistance to Doxorubicin Is Reversed by Mulberry Leaf Polyphenol Extract in Hepatocellular Carcinoma through Inhibition of COX-2
title_sort endoplasmic reticulum stress-induced resistance to doxorubicin is reversed by mulberry leaf polyphenol extract in hepatocellular carcinoma through inhibition of cox-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023226/
https://www.ncbi.nlm.nih.gov/pubmed/31888113
http://dx.doi.org/10.3390/antiox9010026
work_keys_str_mv AT yangmonyuan endoplasmicreticulumstressinducedresistancetodoxorubicinisreversedbymulberryleafpolyphenolextractinhepatocellularcarcinomathroughinhibitionofcox2
AT wuchenghsun endoplasmicreticulumstressinducedresistancetodoxorubicinisreversedbymulberryleafpolyphenolextractinhepatocellularcarcinomathroughinhibitionofcox2
AT hungtungwei endoplasmicreticulumstressinducedresistancetodoxorubicinisreversedbymulberryleafpolyphenolextractinhepatocellularcarcinomathroughinhibitionofcox2
AT wangchaujong endoplasmicreticulumstressinducedresistancetodoxorubicinisreversedbymulberryleafpolyphenolextractinhepatocellularcarcinomathroughinhibitionofcox2