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Orabase-Formulated Benzalkonium Chloride Effectively Suppressed Oral Potentially Malignant Disorder In Vitro and In Vivo
[Image: see text] Oral potentially malignant disorder (OPMD) is associated with an increased risk of progression to oral cancer. Patients with dysplastic changes of the precancerous lesions have a higher malignant transformation rate than those without dysplastic changes. Radiotherapy and surgery ar...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114696/ https://www.ncbi.nlm.nih.gov/pubmed/32258937 http://dx.doi.org/10.1021/acsomega.0c00640 |
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author | Wang, Yen-Yun Xiao, Ling-Yi Chen, Yuk-Kwan Wu, Pao-Chu Chen, Yi-Hua Hu, Stephen Chu-Sung Yuan, Shyng-Shiou F. |
author_facet | Wang, Yen-Yun Xiao, Ling-Yi Chen, Yuk-Kwan Wu, Pao-Chu Chen, Yi-Hua Hu, Stephen Chu-Sung Yuan, Shyng-Shiou F. |
author_sort | Wang, Yen-Yun |
collection | PubMed |
description | [Image: see text] Oral potentially malignant disorder (OPMD) is associated with an increased risk of progression to oral cancer. Patients with dysplastic changes of the precancerous lesions have a higher malignant transformation rate than those without dysplastic changes. Radiotherapy and surgery are the traditionally preferred choices for OPMD treatment. However, side effects caused by radiotherapy and surgery may reduce the willingness of patients to accept therapy. Therefore, developing an Orabase-formulated drug, which can be non-invasively administered, may provide an alternative treatment choice. To find, verify, and develop a new anti-cancer drug cost a lot of time and money, while drug repurposing can shorten both time and cost. In this study, we utilized high-throughput screening library to identify clinical drugs, which may have new bioactivities. Herein, we report that benzalkonium chloride (BAK), an antimicrobial preservative for pharmaceutical products, significantly induced reactive oxygen species production and cell death in oral precancerous cells. Additionally, our results showed that phosphorylation of STAT3 (Tyr705) and Akt (Ser473) were involved in cell death caused by BAK in DOK cells. According to animal studies, the development of DMBA-induced oral precancerous lesions was inhibited by 2% BAK. In conclusion, Orabase-formulated BAK may be a potential treatment for OPMD in the future. |
format | Online Article Text |
id | pubmed-7114696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-71146962020-04-03 Orabase-Formulated Benzalkonium Chloride Effectively Suppressed Oral Potentially Malignant Disorder In Vitro and In Vivo Wang, Yen-Yun Xiao, Ling-Yi Chen, Yuk-Kwan Wu, Pao-Chu Chen, Yi-Hua Hu, Stephen Chu-Sung Yuan, Shyng-Shiou F. ACS Omega [Image: see text] Oral potentially malignant disorder (OPMD) is associated with an increased risk of progression to oral cancer. Patients with dysplastic changes of the precancerous lesions have a higher malignant transformation rate than those without dysplastic changes. Radiotherapy and surgery are the traditionally preferred choices for OPMD treatment. However, side effects caused by radiotherapy and surgery may reduce the willingness of patients to accept therapy. Therefore, developing an Orabase-formulated drug, which can be non-invasively administered, may provide an alternative treatment choice. To find, verify, and develop a new anti-cancer drug cost a lot of time and money, while drug repurposing can shorten both time and cost. In this study, we utilized high-throughput screening library to identify clinical drugs, which may have new bioactivities. Herein, we report that benzalkonium chloride (BAK), an antimicrobial preservative for pharmaceutical products, significantly induced reactive oxygen species production and cell death in oral precancerous cells. Additionally, our results showed that phosphorylation of STAT3 (Tyr705) and Akt (Ser473) were involved in cell death caused by BAK in DOK cells. According to animal studies, the development of DMBA-induced oral precancerous lesions was inhibited by 2% BAK. In conclusion, Orabase-formulated BAK may be a potential treatment for OPMD in the future. American Chemical Society 2020-03-23 /pmc/articles/PMC7114696/ /pubmed/32258937 http://dx.doi.org/10.1021/acsomega.0c00640 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Wang, Yen-Yun Xiao, Ling-Yi Chen, Yuk-Kwan Wu, Pao-Chu Chen, Yi-Hua Hu, Stephen Chu-Sung Yuan, Shyng-Shiou F. Orabase-Formulated Benzalkonium Chloride Effectively Suppressed Oral Potentially Malignant Disorder In Vitro and In Vivo |
title | Orabase-Formulated Benzalkonium Chloride Effectively
Suppressed Oral Potentially Malignant Disorder In Vitro and In Vivo |
title_full | Orabase-Formulated Benzalkonium Chloride Effectively
Suppressed Oral Potentially Malignant Disorder In Vitro and In Vivo |
title_fullStr | Orabase-Formulated Benzalkonium Chloride Effectively
Suppressed Oral Potentially Malignant Disorder In Vitro and In Vivo |
title_full_unstemmed | Orabase-Formulated Benzalkonium Chloride Effectively
Suppressed Oral Potentially Malignant Disorder In Vitro and In Vivo |
title_short | Orabase-Formulated Benzalkonium Chloride Effectively
Suppressed Oral Potentially Malignant Disorder In Vitro and In Vivo |
title_sort | orabase-formulated benzalkonium chloride effectively
suppressed oral potentially malignant disorder in vitro and in vivo |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114696/ https://www.ncbi.nlm.nih.gov/pubmed/32258937 http://dx.doi.org/10.1021/acsomega.0c00640 |
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