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High S100A2 expression in keratinocytes in patients with drug eruption

Telaprevir used as a protease inhibitor against hepatitis C virus is frequently associated with cutaneous adverse reactions. To explore a histological biomarker of cutaneous adverse events induced by telaprevir, we systematically searched for genes that were dysregulated by telaprevir in normal huma...

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Autores principales: Yoshioka, Manabu, Sawada, Yu, Saito-Sasaki, Natsuko, Yoshioka, Haruna, Hama, Kayo, Omoto, Daisuke, Ohmori, Shun, Okada, Etsuko, Nakamura, Motonobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943585/
https://www.ncbi.nlm.nih.gov/pubmed/33750880
http://dx.doi.org/10.1038/s41598-021-85009-8
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author Yoshioka, Manabu
Sawada, Yu
Saito-Sasaki, Natsuko
Yoshioka, Haruna
Hama, Kayo
Omoto, Daisuke
Ohmori, Shun
Okada, Etsuko
Nakamura, Motonobu
author_facet Yoshioka, Manabu
Sawada, Yu
Saito-Sasaki, Natsuko
Yoshioka, Haruna
Hama, Kayo
Omoto, Daisuke
Ohmori, Shun
Okada, Etsuko
Nakamura, Motonobu
author_sort Yoshioka, Manabu
collection PubMed
description Telaprevir used as a protease inhibitor against hepatitis C virus is frequently associated with cutaneous adverse reactions. To explore a histological biomarker of cutaneous adverse events induced by telaprevir, we systematically searched for genes that were dysregulated by telaprevir in normal human epidermal keratinocytes (NHEKs). Microarray analysis and real-time polymerase chain reaction (PCR) revealed the significant increase in the expression of S100 calcium-binding protein A2 (S100A2) gene following treatment of NHEKs with telaprevir. Immunohistochemical analysis demonstrated that the expression of S100A2 was dominant in the spinous layer of the epidermis in patients with telaprevir-mediated severe-type drug eruptions and limited to the basal layer of the epidermis in healthy subjects. Furthermore, S100A2 expression increased after treatment with trichloroethylene and other medications, and the degree of S100A2 expression correlated with the severity of cutaneous adverse events. S100A2 expression also significantly increased in the skin of patients with atopic dermatitis and psoriasis. Taken together, S100A2 is highly expressed in the epidermis under inflammatory conditions and drug eruptions and may serve as a marker for keratinocyte damage in response to any inflammatory or toxic condition.
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spelling pubmed-79435852021-03-10 High S100A2 expression in keratinocytes in patients with drug eruption Yoshioka, Manabu Sawada, Yu Saito-Sasaki, Natsuko Yoshioka, Haruna Hama, Kayo Omoto, Daisuke Ohmori, Shun Okada, Etsuko Nakamura, Motonobu Sci Rep Article Telaprevir used as a protease inhibitor against hepatitis C virus is frequently associated with cutaneous adverse reactions. To explore a histological biomarker of cutaneous adverse events induced by telaprevir, we systematically searched for genes that were dysregulated by telaprevir in normal human epidermal keratinocytes (NHEKs). Microarray analysis and real-time polymerase chain reaction (PCR) revealed the significant increase in the expression of S100 calcium-binding protein A2 (S100A2) gene following treatment of NHEKs with telaprevir. Immunohistochemical analysis demonstrated that the expression of S100A2 was dominant in the spinous layer of the epidermis in patients with telaprevir-mediated severe-type drug eruptions and limited to the basal layer of the epidermis in healthy subjects. Furthermore, S100A2 expression increased after treatment with trichloroethylene and other medications, and the degree of S100A2 expression correlated with the severity of cutaneous adverse events. S100A2 expression also significantly increased in the skin of patients with atopic dermatitis and psoriasis. Taken together, S100A2 is highly expressed in the epidermis under inflammatory conditions and drug eruptions and may serve as a marker for keratinocyte damage in response to any inflammatory or toxic condition. Nature Publishing Group UK 2021-03-09 /pmc/articles/PMC7943585/ /pubmed/33750880 http://dx.doi.org/10.1038/s41598-021-85009-8 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yoshioka, Manabu
Sawada, Yu
Saito-Sasaki, Natsuko
Yoshioka, Haruna
Hama, Kayo
Omoto, Daisuke
Ohmori, Shun
Okada, Etsuko
Nakamura, Motonobu
High S100A2 expression in keratinocytes in patients with drug eruption
title High S100A2 expression in keratinocytes in patients with drug eruption
title_full High S100A2 expression in keratinocytes in patients with drug eruption
title_fullStr High S100A2 expression in keratinocytes in patients with drug eruption
title_full_unstemmed High S100A2 expression in keratinocytes in patients with drug eruption
title_short High S100A2 expression in keratinocytes in patients with drug eruption
title_sort high s100a2 expression in keratinocytes in patients with drug eruption
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943585/
https://www.ncbi.nlm.nih.gov/pubmed/33750880
http://dx.doi.org/10.1038/s41598-021-85009-8
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