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Chemoprevention in oral leukoplakia: challenges and current landscape
Oral potentially malignant disorders have the potential to transform into oral cancer. Oral leukoplakia is a prevalent OPMD with a 9.8% malignant transformation rate. The standard management for OL involves surgical excision, but its efficacy in preventing clinical recurrence and malignant transform...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244562/ https://www.ncbi.nlm.nih.gov/pubmed/37293562 http://dx.doi.org/10.3389/froh.2023.1191347 |
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author | Palma, Victor de Mello Koerich Laureano, Natalia Frank, Luiza Abrahão Rados, Pantelis Varvaki Visioli, Fernanda |
author_facet | Palma, Victor de Mello Koerich Laureano, Natalia Frank, Luiza Abrahão Rados, Pantelis Varvaki Visioli, Fernanda |
author_sort | Palma, Victor de Mello |
collection | PubMed |
description | Oral potentially malignant disorders have the potential to transform into oral cancer. Oral leukoplakia is a prevalent OPMD with a 9.8% malignant transformation rate. The standard management for OL involves surgical excision, but its efficacy in preventing clinical recurrence and malignant transformation is limited. Therefore, alternative strategies such as chemoprevention modalities have emerged as a promising approach to inhibit the carcinogenesis process. The aim of this review was to identify human studies that investigated the effectiveness of chemopreventive agents in preventing the progression of oral leukoplakia and to provide guidance for future research. Several systemic and topical agents have been evaluated for their potential chemopreventive effects in oral leukoplakia. Systemic agents that have been investigated include vitamin A, lycopene, celecoxib, green tea extract, ZengShengPing, Bowman Birk inhibitor, beta-carotene, curcumin, erlotinib, and metformin. In addition, topical agents tested include bleomycin, isotretinoin, ONYX-015 mouthwash, ketorolac, and dried black raspberry. Despite numerous agents that have already been tested, evidence supporting their effectiveness is limited. To improve the search for an ideal chemopreventive agent for oral leukoplakia, we propose several strategies that can be implemented. Oral leukoplakia chemoprevention presents a promising opportunity for decreasing the incidence of oral cancer. Identifying new chemopreventive agents and biomarkers for predicting treatment response should be a focus of future research. |
format | Online Article Text |
id | pubmed-10244562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102445622023-06-08 Chemoprevention in oral leukoplakia: challenges and current landscape Palma, Victor de Mello Koerich Laureano, Natalia Frank, Luiza Abrahão Rados, Pantelis Varvaki Visioli, Fernanda Front Oral Health Oral Health Oral potentially malignant disorders have the potential to transform into oral cancer. Oral leukoplakia is a prevalent OPMD with a 9.8% malignant transformation rate. The standard management for OL involves surgical excision, but its efficacy in preventing clinical recurrence and malignant transformation is limited. Therefore, alternative strategies such as chemoprevention modalities have emerged as a promising approach to inhibit the carcinogenesis process. The aim of this review was to identify human studies that investigated the effectiveness of chemopreventive agents in preventing the progression of oral leukoplakia and to provide guidance for future research. Several systemic and topical agents have been evaluated for their potential chemopreventive effects in oral leukoplakia. Systemic agents that have been investigated include vitamin A, lycopene, celecoxib, green tea extract, ZengShengPing, Bowman Birk inhibitor, beta-carotene, curcumin, erlotinib, and metformin. In addition, topical agents tested include bleomycin, isotretinoin, ONYX-015 mouthwash, ketorolac, and dried black raspberry. Despite numerous agents that have already been tested, evidence supporting their effectiveness is limited. To improve the search for an ideal chemopreventive agent for oral leukoplakia, we propose several strategies that can be implemented. Oral leukoplakia chemoprevention presents a promising opportunity for decreasing the incidence of oral cancer. Identifying new chemopreventive agents and biomarkers for predicting treatment response should be a focus of future research. Frontiers Media S.A. 2023-05-24 /pmc/articles/PMC10244562/ /pubmed/37293562 http://dx.doi.org/10.3389/froh.2023.1191347 Text en © 2023 Palma, Koerich Laureano, Frank, Rados and Visioli. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oral Health Palma, Victor de Mello Koerich Laureano, Natalia Frank, Luiza Abrahão Rados, Pantelis Varvaki Visioli, Fernanda Chemoprevention in oral leukoplakia: challenges and current landscape |
title | Chemoprevention in oral leukoplakia: challenges and current landscape |
title_full | Chemoprevention in oral leukoplakia: challenges and current landscape |
title_fullStr | Chemoprevention in oral leukoplakia: challenges and current landscape |
title_full_unstemmed | Chemoprevention in oral leukoplakia: challenges and current landscape |
title_short | Chemoprevention in oral leukoplakia: challenges and current landscape |
title_sort | chemoprevention in oral leukoplakia: challenges and current landscape |
topic | Oral Health |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244562/ https://www.ncbi.nlm.nih.gov/pubmed/37293562 http://dx.doi.org/10.3389/froh.2023.1191347 |
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