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Tirbanibulin for Actinic Keratosis: Insights into the Mechanism of Action
Actinic keratosis (AK) is a common pre-neoplastic skin lesion constituted by uncontrolled proliferation of atypical keratinocytes that may evolve to squamous cell carcinoma. With global prevalence increasing, AK is expected to be the most common carcinoma of the skin. Tirbanibulin is a reversible tu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675993/ https://www.ncbi.nlm.nih.gov/pubmed/36415541 http://dx.doi.org/10.2147/CCID.S374122 |
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author | Schlesinger, Todd Stockfleth, Eggert Grada, Ayman Berman, Brian |
author_facet | Schlesinger, Todd Stockfleth, Eggert Grada, Ayman Berman, Brian |
author_sort | Schlesinger, Todd |
collection | PubMed |
description | Actinic keratosis (AK) is a common pre-neoplastic skin lesion constituted by uncontrolled proliferation of atypical keratinocytes that may evolve to squamous cell carcinoma. With global prevalence increasing, AK is expected to be the most common carcinoma of the skin. Tirbanibulin is a reversible tubulin polymerization inhibitor with potent anti-proliferative and anti-tumoral effects. In-vivo and in-vitro studies have shown that tirbanibulin significantly inhibits cell proliferation, tumor growth and downregulates Src signaling with no overt toxicity. Early phase and Phase III trials have shown high lesion clearance, compliance, and few side effects of once daily tirbanibulin treatment. This review discusses tirbanibulin anti-cancer activity, focusing on tubulin polymerization and Src signaling inhibitory effects, highlighting relevant literature and novel preclinical results from the ATNXUS-KX01-001 study. Furthermore, we address the relevant findings obtained in recent clinical trials to evaluate the safety, efficacy, pharmacokinetics, clearance efficacy, and side effects of the 1% tirbanibulin ointment applied once daily. In summary, we highlight preclinical and clinical evidence on the use of tirbanibulin as an effective and safe treatment option for AK. |
format | Online Article Text |
id | pubmed-9675993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-96759932022-11-21 Tirbanibulin for Actinic Keratosis: Insights into the Mechanism of Action Schlesinger, Todd Stockfleth, Eggert Grada, Ayman Berman, Brian Clin Cosmet Investig Dermatol Review Actinic keratosis (AK) is a common pre-neoplastic skin lesion constituted by uncontrolled proliferation of atypical keratinocytes that may evolve to squamous cell carcinoma. With global prevalence increasing, AK is expected to be the most common carcinoma of the skin. Tirbanibulin is a reversible tubulin polymerization inhibitor with potent anti-proliferative and anti-tumoral effects. In-vivo and in-vitro studies have shown that tirbanibulin significantly inhibits cell proliferation, tumor growth and downregulates Src signaling with no overt toxicity. Early phase and Phase III trials have shown high lesion clearance, compliance, and few side effects of once daily tirbanibulin treatment. This review discusses tirbanibulin anti-cancer activity, focusing on tubulin polymerization and Src signaling inhibitory effects, highlighting relevant literature and novel preclinical results from the ATNXUS-KX01-001 study. Furthermore, we address the relevant findings obtained in recent clinical trials to evaluate the safety, efficacy, pharmacokinetics, clearance efficacy, and side effects of the 1% tirbanibulin ointment applied once daily. In summary, we highlight preclinical and clinical evidence on the use of tirbanibulin as an effective and safe treatment option for AK. Dove 2022-11-16 /pmc/articles/PMC9675993/ /pubmed/36415541 http://dx.doi.org/10.2147/CCID.S374122 Text en © 2022 Schlesinger et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Review Schlesinger, Todd Stockfleth, Eggert Grada, Ayman Berman, Brian Tirbanibulin for Actinic Keratosis: Insights into the Mechanism of Action |
title | Tirbanibulin for Actinic Keratosis: Insights into the Mechanism of Action |
title_full | Tirbanibulin for Actinic Keratosis: Insights into the Mechanism of Action |
title_fullStr | Tirbanibulin for Actinic Keratosis: Insights into the Mechanism of Action |
title_full_unstemmed | Tirbanibulin for Actinic Keratosis: Insights into the Mechanism of Action |
title_short | Tirbanibulin for Actinic Keratosis: Insights into the Mechanism of Action |
title_sort | tirbanibulin for actinic keratosis: insights into the mechanism of action |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675993/ https://www.ncbi.nlm.nih.gov/pubmed/36415541 http://dx.doi.org/10.2147/CCID.S374122 |
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