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Biomarkers of basal cell carcinoma resistance to methyl-aminolevulinate photodynamic therapy

BACKGROUND: Methyl-aminolevulinate photodynamic therapy (MAL-PDT) is an excellent option for the treatment of basal cell carcinoma (BCC). However, up to 25% of cases are resistant to this treatment modality. OBJECTIVE: The aim of this study was to identify potential biomarkers of BCC response to MAL...

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Autores principales: Gracia-Cazaña, Tamara, Mascaraque, Marta, Lucena, Silvia Rocío, Vera-Álvarez, Jesús, González, Salvador, Juarranz, Ángeles, Gilaberte, Yolanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6481917/
https://www.ncbi.nlm.nih.gov/pubmed/31017970
http://dx.doi.org/10.1371/journal.pone.0215537
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author Gracia-Cazaña, Tamara
Mascaraque, Marta
Lucena, Silvia Rocío
Vera-Álvarez, Jesús
González, Salvador
Juarranz, Ángeles
Gilaberte, Yolanda
author_facet Gracia-Cazaña, Tamara
Mascaraque, Marta
Lucena, Silvia Rocío
Vera-Álvarez, Jesús
González, Salvador
Juarranz, Ángeles
Gilaberte, Yolanda
author_sort Gracia-Cazaña, Tamara
collection PubMed
description BACKGROUND: Methyl-aminolevulinate photodynamic therapy (MAL-PDT) is an excellent option for the treatment of basal cell carcinoma (BCC). However, up to 25% of cases are resistant to this treatment modality. OBJECTIVE: The aim of this study was to identify potential biomarkers of BCC response to MAL-PDT. MATERIAL AND METHODS: Clinical, histological, and immunohistochemical (p53, Ki-67, CD-31, COX2, β-catenin, EGFR, and survivin) variables were analyzed in a retrospective study of consecutive BCC patients treated with MAL-PDT at the San Jorge Hospital, Huesca, Spain between January 2006 and December 2015. To deepen on these markers, the effects on p53 and cyclin D1 expression, in vitro response to MAL-PDT of 2 murine BCC cell lines (ASZ and BSZ), was also evaluated. RESULTS: The retrospective study examined the response to MAL-PDT of 390 BCCs from 182 patients. The overall clinical response rate was 82.8%, with a mean follow-up time of 35.96 months (SD = 23.46). Immunohistochemistry revealed positive p53 in 84.6% of responders but only 15.4% of nonresponsive tumors (p = 0.011). Tumors with increased peripheral palisading of basal cell islands to immunostaining β-catenin responded poorly to PDT (p = 0.01). In line with our findings in patients, in vitro studies revealed a better response to PDT in the p53-positive ASZ cell line than the p53-negative BSZ cell line (p<0.01). Multivariate analysis revealed that the following variables were significantly associated with response to PDT: age, nBCC, presence of peritumoral inflammatory infiltrate, and p53 immunopositivity. Patients with positive p53 immunostaining were 68.54 times more likely to achieve cure than p53-negative patients (CI95% 2.94–159.8) CONCLUSION: Our finding suggest that certain clinicopathological and immunohistochemical variables, particularly p53 expression, may serve as indicators of BCC response to MAL-PDT, and thus facilitate the selection of patients who are most likely to benefit from this therapy.
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spelling pubmed-64819172019-05-07 Biomarkers of basal cell carcinoma resistance to methyl-aminolevulinate photodynamic therapy Gracia-Cazaña, Tamara Mascaraque, Marta Lucena, Silvia Rocío Vera-Álvarez, Jesús González, Salvador Juarranz, Ángeles Gilaberte, Yolanda PLoS One Research Article BACKGROUND: Methyl-aminolevulinate photodynamic therapy (MAL-PDT) is an excellent option for the treatment of basal cell carcinoma (BCC). However, up to 25% of cases are resistant to this treatment modality. OBJECTIVE: The aim of this study was to identify potential biomarkers of BCC response to MAL-PDT. MATERIAL AND METHODS: Clinical, histological, and immunohistochemical (p53, Ki-67, CD-31, COX2, β-catenin, EGFR, and survivin) variables were analyzed in a retrospective study of consecutive BCC patients treated with MAL-PDT at the San Jorge Hospital, Huesca, Spain between January 2006 and December 2015. To deepen on these markers, the effects on p53 and cyclin D1 expression, in vitro response to MAL-PDT of 2 murine BCC cell lines (ASZ and BSZ), was also evaluated. RESULTS: The retrospective study examined the response to MAL-PDT of 390 BCCs from 182 patients. The overall clinical response rate was 82.8%, with a mean follow-up time of 35.96 months (SD = 23.46). Immunohistochemistry revealed positive p53 in 84.6% of responders but only 15.4% of nonresponsive tumors (p = 0.011). Tumors with increased peripheral palisading of basal cell islands to immunostaining β-catenin responded poorly to PDT (p = 0.01). In line with our findings in patients, in vitro studies revealed a better response to PDT in the p53-positive ASZ cell line than the p53-negative BSZ cell line (p<0.01). Multivariate analysis revealed that the following variables were significantly associated with response to PDT: age, nBCC, presence of peritumoral inflammatory infiltrate, and p53 immunopositivity. Patients with positive p53 immunostaining were 68.54 times more likely to achieve cure than p53-negative patients (CI95% 2.94–159.8) CONCLUSION: Our finding suggest that certain clinicopathological and immunohistochemical variables, particularly p53 expression, may serve as indicators of BCC response to MAL-PDT, and thus facilitate the selection of patients who are most likely to benefit from this therapy. Public Library of Science 2019-04-24 /pmc/articles/PMC6481917/ /pubmed/31017970 http://dx.doi.org/10.1371/journal.pone.0215537 Text en © 2019 Gracia-Cazaña et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gracia-Cazaña, Tamara
Mascaraque, Marta
Lucena, Silvia Rocío
Vera-Álvarez, Jesús
González, Salvador
Juarranz, Ángeles
Gilaberte, Yolanda
Biomarkers of basal cell carcinoma resistance to methyl-aminolevulinate photodynamic therapy
title Biomarkers of basal cell carcinoma resistance to methyl-aminolevulinate photodynamic therapy
title_full Biomarkers of basal cell carcinoma resistance to methyl-aminolevulinate photodynamic therapy
title_fullStr Biomarkers of basal cell carcinoma resistance to methyl-aminolevulinate photodynamic therapy
title_full_unstemmed Biomarkers of basal cell carcinoma resistance to methyl-aminolevulinate photodynamic therapy
title_short Biomarkers of basal cell carcinoma resistance to methyl-aminolevulinate photodynamic therapy
title_sort biomarkers of basal cell carcinoma resistance to methyl-aminolevulinate photodynamic therapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6481917/
https://www.ncbi.nlm.nih.gov/pubmed/31017970
http://dx.doi.org/10.1371/journal.pone.0215537
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