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Natural Compounds Modulate Drug Transporter Mediated Oral Cancer Treatment
Oral cancer (OC) is a serious health problem. Surgery is the best method to treat the disease but might reduce the quality of life of patients. Photodynamic therapy (PDT) may enhance quality of life but with some limitations. Therefore, the development of a new strategy to facilitate PDT effectivene...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565123/ https://www.ncbi.nlm.nih.gov/pubmed/32957726 http://dx.doi.org/10.3390/biom10091335 |
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author | Yang, Hsiang Wei, Yu-Ching Li, Wan-Chun Chen, Hsin-Yung Lin, Hung-Ying Chiang, Chun-Pin Chen, Hsin-Ming |
author_facet | Yang, Hsiang Wei, Yu-Ching Li, Wan-Chun Chen, Hsin-Yung Lin, Hung-Ying Chiang, Chun-Pin Chen, Hsin-Ming |
author_sort | Yang, Hsiang |
collection | PubMed |
description | Oral cancer (OC) is a serious health problem. Surgery is the best method to treat the disease but might reduce the quality of life of patients. Photodynamic therapy (PDT) may enhance quality of life but with some limitations. Therefore, the development of a new strategy to facilitate PDT effectiveness has become crucial. ATP-binding cassette G2 (ABCG2) is a membrane protein-associated drug resistance and stemness in cancers. Here, we examined whether ABCG2 plays an important role in regulating the treatment efficacy of PDT and whether ABCG2 inhibition by natural compounds can promote the effect of PDT in OC cells. Several head and neck cancer cells were utilized in this study. OECM1 and SAS cells were selected to investigate the relationship between ABCG2 expression and protoporphyrin IX (PpIX) accumulation. Western blot analysis, flow cytometry analysis, and survival probability were performed to determine PDT efficacy and cellular stemness upon treatment of different dietary compounds, including epigallocatechin gallate (EGCG) and curcumin. In this study, we found that ABCG2 expression varied in OC cells. Hypoglycemic culture for SAS cells enhanced ABCG2 expression as higher ABCG2 expression was associated with lower PpIX accumulation and cellular stemness in OC cells. In contrast, suppression of ABCG2 expression by curcumin and tea polyphenol EGCG led to greater PpIX accumulation and enhanced PDT treatment efficiency in OC cells. In conclusion, ABCG2 plays an important role in regulating the effect of PDT. Change in glucose concentration and treatment with natural compounds modulated ABCG2 expression, resulting in altered PDT efficacy for OC cells. These modulations raise a potential new treatment strategy for early-stage OCs. |
format | Online Article Text |
id | pubmed-7565123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75651232020-10-26 Natural Compounds Modulate Drug Transporter Mediated Oral Cancer Treatment Yang, Hsiang Wei, Yu-Ching Li, Wan-Chun Chen, Hsin-Yung Lin, Hung-Ying Chiang, Chun-Pin Chen, Hsin-Ming Biomolecules Article Oral cancer (OC) is a serious health problem. Surgery is the best method to treat the disease but might reduce the quality of life of patients. Photodynamic therapy (PDT) may enhance quality of life but with some limitations. Therefore, the development of a new strategy to facilitate PDT effectiveness has become crucial. ATP-binding cassette G2 (ABCG2) is a membrane protein-associated drug resistance and stemness in cancers. Here, we examined whether ABCG2 plays an important role in regulating the treatment efficacy of PDT and whether ABCG2 inhibition by natural compounds can promote the effect of PDT in OC cells. Several head and neck cancer cells were utilized in this study. OECM1 and SAS cells were selected to investigate the relationship between ABCG2 expression and protoporphyrin IX (PpIX) accumulation. Western blot analysis, flow cytometry analysis, and survival probability were performed to determine PDT efficacy and cellular stemness upon treatment of different dietary compounds, including epigallocatechin gallate (EGCG) and curcumin. In this study, we found that ABCG2 expression varied in OC cells. Hypoglycemic culture for SAS cells enhanced ABCG2 expression as higher ABCG2 expression was associated with lower PpIX accumulation and cellular stemness in OC cells. In contrast, suppression of ABCG2 expression by curcumin and tea polyphenol EGCG led to greater PpIX accumulation and enhanced PDT treatment efficiency in OC cells. In conclusion, ABCG2 plays an important role in regulating the effect of PDT. Change in glucose concentration and treatment with natural compounds modulated ABCG2 expression, resulting in altered PDT efficacy for OC cells. These modulations raise a potential new treatment strategy for early-stage OCs. MDPI 2020-09-17 /pmc/articles/PMC7565123/ /pubmed/32957726 http://dx.doi.org/10.3390/biom10091335 Text en © 2020 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, Hsiang Wei, Yu-Ching Li, Wan-Chun Chen, Hsin-Yung Lin, Hung-Ying Chiang, Chun-Pin Chen, Hsin-Ming Natural Compounds Modulate Drug Transporter Mediated Oral Cancer Treatment |
title | Natural Compounds Modulate Drug Transporter Mediated Oral Cancer Treatment |
title_full | Natural Compounds Modulate Drug Transporter Mediated Oral Cancer Treatment |
title_fullStr | Natural Compounds Modulate Drug Transporter Mediated Oral Cancer Treatment |
title_full_unstemmed | Natural Compounds Modulate Drug Transporter Mediated Oral Cancer Treatment |
title_short | Natural Compounds Modulate Drug Transporter Mediated Oral Cancer Treatment |
title_sort | natural compounds modulate drug transporter mediated oral cancer treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565123/ https://www.ncbi.nlm.nih.gov/pubmed/32957726 http://dx.doi.org/10.3390/biom10091335 |
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