GATA‐binding protein 3 and gross cystic disease fluid protein 15 as a potential diagnostic marker for extramammary Paget's disease

Abstract Objectives The aim of this study was to evaluate the expression of GCDFP15 and GATA‐binding protein 3 (GATA‐3) in extramammary Paget's disease (EMPD) skin and serum samples and to assess their availability as tumor markers for the diagnosis and assessment of disease severity in primary...

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Autores principales: Soichiro Kado, Koji Kamiya, Meijuan Jin, Miho Kimura, Md Razib Hossain, Takeo Maekawa, Mayumi Komine, Mamitaro Ohtsuki
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Lenguaje:EN
Publicado: Wiley 2021
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spelling oai:doaj.org-article:52d6ac78eedc41268d961a26aacb651c2021-12-02T09:08:29ZGATA‐binding protein 3 and gross cystic disease fluid protein 15 as a potential diagnostic marker for extramammary Paget's disease2574-459310.1002/cia2.12193https://doaj.org/article/52d6ac78eedc41268d961a26aacb651c2021-12-01T00:00:00Zhttps://doi.org/10.1002/cia2.12193https://doaj.org/toc/2574-4593Abstract Objectives The aim of this study was to evaluate the expression of GCDFP15 and GATA‐binding protein 3 (GATA‐3) in extramammary Paget's disease (EMPD) skin and serum samples and to assess their availability as tumor markers for the diagnosis and assessment of disease severity in primary EMPD. Methods Skin samples and serum samples were obtained from 16 patients with primary EMPD (10 cases from male, six cases from female; stage IA six cases, stage IB seven cases, stage III one case, stage IV two cases). By immunohistochemistry, the expression of GCDFP15 and GATA3 was examined in skin specimens. The serum levels of GCDFP15 and GATA3 were quantified by ELISA. Results In our study, eight out of 16 patients showed positive staining for GCDFP15. In contrast, all 16 patients showed positive staining for GATA‐3. Immunohistochemical staining of EMPD skin samples showed that GATA‐3 had a higher positivity rate than GCDFP15. However, there was no correlation between serum levels of GCDFP15 or GATA‐3 and the disease stage. Conclusion Our results indicate that GCDFP15 and GATA‐3 are useful for the diagnosis of primary EMPD, but not for monitoring disease progression, and suggest that GATA‐3 is a more reliable marker than GCDFP15 for the diagnosis of primary EMPD.Soichiro KadoKoji KamiyaMeijuan JinMiho KimuraMd Razib HossainTakeo MaekawaMayumi KomineMamitaro OhtsukiWileyarticledermatologydiagnosisimmunohistochemistryPaget diseaseextramammarysensitivity and specificityDermatologyRL1-803Immunologic diseases. AllergyRC581-607ENJournal of Cutaneous Immunology and Allergy, Vol 4, Iss 6, Pp 154-158 (2021)
institution DOAJ
collection DOAJ
language EN
topic dermatology
diagnosis
immunohistochemistry
Paget disease
extramammary
sensitivity and specificity
Dermatology
RL1-803
Immunologic diseases. Allergy
RC581-607
spellingShingle dermatology
diagnosis
immunohistochemistry
Paget disease
extramammary
sensitivity and specificity
Dermatology
RL1-803
Immunologic diseases. Allergy
RC581-607
Soichiro Kado
Koji Kamiya
Meijuan Jin
Miho Kimura
Md Razib Hossain
Takeo Maekawa
Mayumi Komine
Mamitaro Ohtsuki
GATA‐binding protein 3 and gross cystic disease fluid protein 15 as a potential diagnostic marker for extramammary Paget's disease
description Abstract Objectives The aim of this study was to evaluate the expression of GCDFP15 and GATA‐binding protein 3 (GATA‐3) in extramammary Paget's disease (EMPD) skin and serum samples and to assess their availability as tumor markers for the diagnosis and assessment of disease severity in primary EMPD. Methods Skin samples and serum samples were obtained from 16 patients with primary EMPD (10 cases from male, six cases from female; stage IA six cases, stage IB seven cases, stage III one case, stage IV two cases). By immunohistochemistry, the expression of GCDFP15 and GATA3 was examined in skin specimens. The serum levels of GCDFP15 and GATA3 were quantified by ELISA. Results In our study, eight out of 16 patients showed positive staining for GCDFP15. In contrast, all 16 patients showed positive staining for GATA‐3. Immunohistochemical staining of EMPD skin samples showed that GATA‐3 had a higher positivity rate than GCDFP15. However, there was no correlation between serum levels of GCDFP15 or GATA‐3 and the disease stage. Conclusion Our results indicate that GCDFP15 and GATA‐3 are useful for the diagnosis of primary EMPD, but not for monitoring disease progression, and suggest that GATA‐3 is a more reliable marker than GCDFP15 for the diagnosis of primary EMPD.
format article
author Soichiro Kado
Koji Kamiya
Meijuan Jin
Miho Kimura
Md Razib Hossain
Takeo Maekawa
Mayumi Komine
Mamitaro Ohtsuki
author_facet Soichiro Kado
Koji Kamiya
Meijuan Jin
Miho Kimura
Md Razib Hossain
Takeo Maekawa
Mayumi Komine
Mamitaro Ohtsuki
author_sort Soichiro Kado
title GATA‐binding protein 3 and gross cystic disease fluid protein 15 as a potential diagnostic marker for extramammary Paget's disease
title_short GATA‐binding protein 3 and gross cystic disease fluid protein 15 as a potential diagnostic marker for extramammary Paget's disease
title_full GATA‐binding protein 3 and gross cystic disease fluid protein 15 as a potential diagnostic marker for extramammary Paget's disease
title_fullStr GATA‐binding protein 3 and gross cystic disease fluid protein 15 as a potential diagnostic marker for extramammary Paget's disease
title_full_unstemmed GATA‐binding protein 3 and gross cystic disease fluid protein 15 as a potential diagnostic marker for extramammary Paget's disease
title_sort gata‐binding protein 3 and gross cystic disease fluid protein 15 as a potential diagnostic marker for extramammary paget's disease
publisher Wiley
publishDate 2021
url https://doaj.org/article/52d6ac78eedc41268d961a26aacb651c
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