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CDK4: A Novel Therapeutic Target for Extramammary Paget’s Disease
BACKGROUND: The outcome of extramammary Paget’s disease (EMPD) is poor when it progresses to metastasis because of the lack of effective systemic therapies. Recently, CDK4-targeted therapy has attracted attention as a potential therapeutic target for some cancers. The aim of this study was to analyz...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358779/ https://www.ncbi.nlm.nih.gov/pubmed/34395284 http://dx.doi.org/10.3389/fonc.2021.710378 |
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author | Hashimoto, Hiroki Kaku-Ito, Yumiko Oda, Yoshinao Ito, Takamichi |
author_facet | Hashimoto, Hiroki Kaku-Ito, Yumiko Oda, Yoshinao Ito, Takamichi |
author_sort | Hashimoto, Hiroki |
collection | PubMed |
description | BACKGROUND: The outcome of extramammary Paget’s disease (EMPD) is poor when it progresses to metastasis because of the lack of effective systemic therapies. Recently, CDK4-targeted therapy has attracted attention as a potential therapeutic target for some cancers. The aim of this study was to analyze the impact of CDK4 expression on the survival of patients with EMPD. METHODS: We retrospectively reviewed 110 patients with EMPD. We conducted immunohistochemical analysis of CDK4 and cyclin D1 expression, and assessed the association between their expression and survival. RESULTS: Most EMPD lesions (108/110, 98.2%) were positive for CDK4 staining and there was a positive correlation between CDK4 expression and cyclin D1 expression (r = 0.54, p < 0.001). Tumor thickness (p = 0.0003) and the presence of regional lymph node metastasis (p = 0.015) were significantly associated with high CDK4 expression. Regarding invasive EMPD, the multivariate analysis did not show the correlation between the expression of CDK4/cyclin D1 and survival outcomes (HR: 3.14, p = 0.14). CONCLUSION: The overexpression of CDK4 was identified as a major risk factor for disease progression. CDK4-targeted therapy could thus be a novel treatment option for unresectable EMPD. |
format | Online Article Text |
id | pubmed-8358779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83587792021-08-13 CDK4: A Novel Therapeutic Target for Extramammary Paget’s Disease Hashimoto, Hiroki Kaku-Ito, Yumiko Oda, Yoshinao Ito, Takamichi Front Oncol Oncology BACKGROUND: The outcome of extramammary Paget’s disease (EMPD) is poor when it progresses to metastasis because of the lack of effective systemic therapies. Recently, CDK4-targeted therapy has attracted attention as a potential therapeutic target for some cancers. The aim of this study was to analyze the impact of CDK4 expression on the survival of patients with EMPD. METHODS: We retrospectively reviewed 110 patients with EMPD. We conducted immunohistochemical analysis of CDK4 and cyclin D1 expression, and assessed the association between their expression and survival. RESULTS: Most EMPD lesions (108/110, 98.2%) were positive for CDK4 staining and there was a positive correlation between CDK4 expression and cyclin D1 expression (r = 0.54, p < 0.001). Tumor thickness (p = 0.0003) and the presence of regional lymph node metastasis (p = 0.015) were significantly associated with high CDK4 expression. Regarding invasive EMPD, the multivariate analysis did not show the correlation between the expression of CDK4/cyclin D1 and survival outcomes (HR: 3.14, p = 0.14). CONCLUSION: The overexpression of CDK4 was identified as a major risk factor for disease progression. CDK4-targeted therapy could thus be a novel treatment option for unresectable EMPD. Frontiers Media S.A. 2021-07-29 /pmc/articles/PMC8358779/ /pubmed/34395284 http://dx.doi.org/10.3389/fonc.2021.710378 Text en Copyright © 2021 Hashimoto, Kaku-Ito, Oda and Ito 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). 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 | Oncology Hashimoto, Hiroki Kaku-Ito, Yumiko Oda, Yoshinao Ito, Takamichi CDK4: A Novel Therapeutic Target for Extramammary Paget’s Disease |
title | CDK4: A Novel Therapeutic Target for Extramammary Paget’s Disease |
title_full | CDK4: A Novel Therapeutic Target for Extramammary Paget’s Disease |
title_fullStr | CDK4: A Novel Therapeutic Target for Extramammary Paget’s Disease |
title_full_unstemmed | CDK4: A Novel Therapeutic Target for Extramammary Paget’s Disease |
title_short | CDK4: A Novel Therapeutic Target for Extramammary Paget’s Disease |
title_sort | cdk4: a novel therapeutic target for extramammary paget’s disease |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358779/ https://www.ncbi.nlm.nih.gov/pubmed/34395284 http://dx.doi.org/10.3389/fonc.2021.710378 |
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