Dihydromyricetin Exhibits Antitumor Activity in Nasopharyngeal Cancer Cell Through Antagonizing Wnt/β-catenin Signaling

Background: Cancer stem cells (CSCs) have been demonstrated to play a vital role in a diversity of biological processes in cancers. With the emergence of new evidence, the important function of CSCs in the formation of multidrug resistance of nasopharyngeal cancer has been demonstrated. Dysregulated...

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Main Authors: Ling Ye, Gendi Yin, Miaohua Jiang, Bo Tu, Zhicheng Li, Yiming Wang
Format: Article
Language:English
Published: SAGE Publishing 2021-03-01
Series:Integrative Cancer Therapies
Online Access:https://doi.org/10.1177/1534735421991217
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spelling doaj-c7a3e6c996eb47ac9001c09671c366112021-03-16T22:33:23ZengSAGE PublishingIntegrative Cancer Therapies1534-73541552-695X2021-03-012010.1177/1534735421991217Dihydromyricetin Exhibits Antitumor Activity in Nasopharyngeal Cancer Cell Through Antagonizing Wnt/β-catenin SignalingLing Ye0Gendi Yin1Miaohua Jiang2Bo Tu3Zhicheng Li4Yiming Wang5The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, ChinaThe Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, ChinaThe First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, ChinaThe First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, ChinaThe Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, ChinaThe First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, ChinaBackground: Cancer stem cells (CSCs) have been demonstrated to play a vital role in a diversity of biological processes in cancers. With the emergence of new evidence, the important function of CSCs in the formation of multidrug resistance of nasopharyngeal cancer has been demonstrated. Dysregulated Wnt/β-catenin signaling pathway is an important contributor to chemoresistance and maintenance of CSCs-like characteristics. This research aims to investigate comprehensively the function of dihydromyricetin (DMY), a natural flavonoid drug, on the cisplatin (cis) resistance and stem cell properties of nasopharyngeal cancer. Methods: In this study, the functional role of DMY in nasopharyngeal cancer progression was comprehensively investigated in vitro and in vivo, and then its relationship with CSCs-like phenotypes and multiple oncogenes was analyzed. Results: In parallel assays, the growth inhibitory action of cis was enhanced by the addition of DMY in cis-resistant nasopharyngeal cancer cell lines (Hone1/cis and CNE1/cis). Functional assays showed that DMY markedly diminished the stem cell properties of nasopharyngeal cells, such as colony and tumor-sphere formation. In vivo data showed that the growth of Hone1 CSCs formed tumor xenograft was inhibited significantly by the administration of DMY. Additionally, DMY could impair the Wnt/β-catenin signaling pathway and regulate the expression of downstream proteins in nasopharyngeal cancer cells. Conclusions: Our study clarified the anti-tumor activity of DMY through blocking the Wnt/β-catenin signaling pathway in nasopharyngeal cancer. Therefore, DMY could be a novel therapeutic agent for nasopharyngeal cancer treatment.https://doi.org/10.1177/1534735421991217
collection DOAJ
language English
format Article
sources DOAJ
author Ling Ye
Gendi Yin
Miaohua Jiang
Bo Tu
Zhicheng Li
Yiming Wang
spellingShingle Ling Ye
Gendi Yin
Miaohua Jiang
Bo Tu
Zhicheng Li
Yiming Wang
Dihydromyricetin Exhibits Antitumor Activity in Nasopharyngeal Cancer Cell Through Antagonizing Wnt/β-catenin Signaling
Integrative Cancer Therapies
author_facet Ling Ye
Gendi Yin
Miaohua Jiang
Bo Tu
Zhicheng Li
Yiming Wang
author_sort Ling Ye
title Dihydromyricetin Exhibits Antitumor Activity in Nasopharyngeal Cancer Cell Through Antagonizing Wnt/β-catenin Signaling
title_short Dihydromyricetin Exhibits Antitumor Activity in Nasopharyngeal Cancer Cell Through Antagonizing Wnt/β-catenin Signaling
title_full Dihydromyricetin Exhibits Antitumor Activity in Nasopharyngeal Cancer Cell Through Antagonizing Wnt/β-catenin Signaling
title_fullStr Dihydromyricetin Exhibits Antitumor Activity in Nasopharyngeal Cancer Cell Through Antagonizing Wnt/β-catenin Signaling
title_full_unstemmed Dihydromyricetin Exhibits Antitumor Activity in Nasopharyngeal Cancer Cell Through Antagonizing Wnt/β-catenin Signaling
title_sort dihydromyricetin exhibits antitumor activity in nasopharyngeal cancer cell through antagonizing wnt/β-catenin signaling
publisher SAGE Publishing
series Integrative Cancer Therapies
issn 1534-7354
1552-695X
publishDate 2021-03-01
description Background: Cancer stem cells (CSCs) have been demonstrated to play a vital role in a diversity of biological processes in cancers. With the emergence of new evidence, the important function of CSCs in the formation of multidrug resistance of nasopharyngeal cancer has been demonstrated. Dysregulated Wnt/β-catenin signaling pathway is an important contributor to chemoresistance and maintenance of CSCs-like characteristics. This research aims to investigate comprehensively the function of dihydromyricetin (DMY), a natural flavonoid drug, on the cisplatin (cis) resistance and stem cell properties of nasopharyngeal cancer. Methods: In this study, the functional role of DMY in nasopharyngeal cancer progression was comprehensively investigated in vitro and in vivo, and then its relationship with CSCs-like phenotypes and multiple oncogenes was analyzed. Results: In parallel assays, the growth inhibitory action of cis was enhanced by the addition of DMY in cis-resistant nasopharyngeal cancer cell lines (Hone1/cis and CNE1/cis). Functional assays showed that DMY markedly diminished the stem cell properties of nasopharyngeal cells, such as colony and tumor-sphere formation. In vivo data showed that the growth of Hone1 CSCs formed tumor xenograft was inhibited significantly by the administration of DMY. Additionally, DMY could impair the Wnt/β-catenin signaling pathway and regulate the expression of downstream proteins in nasopharyngeal cancer cells. Conclusions: Our study clarified the anti-tumor activity of DMY through blocking the Wnt/β-catenin signaling pathway in nasopharyngeal cancer. Therefore, DMY could be a novel therapeutic agent for nasopharyngeal cancer treatment.
url https://doi.org/10.1177/1534735421991217
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