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Different Immunohistochemical Localization of Fatty Acid Binding Protein 5 in Actinic Keratosis Compared with That in Bowen's Disease: A Retrospective Study

Authors
Ahn, BokyungKim, Chul HwanChae, Yang-SeokLee, Jeong HyeonLee, YoungseokAhn, Hyo HyunLee, Yoo Jin
Issue Date
5월-2021
Publisher
LIPPINCOTT WILLIAMS & WILKINS
Keywords
actinic keratosis; Bowen' s disease; fatty acid-binding protein 5; FABP5; tumorigenesis
Citation
AMERICAN JOURNAL OF DERMATOPATHOLOGY, v.43, no.5, pp.356 - 361
Indexed
SCIE
SCOPUS
Journal Title
AMERICAN JOURNAL OF DERMATOPATHOLOGY
Volume
43
Number
5
Start Page
356
End Page
361
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/128103
DOI
10.1097/DAD.0000000000001823
ISSN
0193-1091
Abstract
Actinic keratosis (AK) and Bowen's disease (BD) are common premalignant lesions of invasive squamous cell carcinoma that have different pathogenesis and clinical significance. Fatty acid-binding protein 5 (FABP5) is responsible for keratinocyte homeostasis and differentiation; however, no study has revealed its expression in AK and BD. Our study aimed to investigate the differential expression and significance of FABP5 in these lesions. Patients with pathologically confirmed cases of AK (n = 37) and BD (n = 12) were included in this study. FABP5 immunostaining pattern was assessed in the normal skin, AK and BD lesions, with a focus on the staining patterns of basal cells, atypical keratinocytes, and uninvolved epidermal keratinocytes. All patients with AK showed negative FABP5 expression in the atypical cells in the basal layer, whereas the uninvolved upper layers showed diffuse, strong FABP5 expression, regardless of the grade of AK. All patients with BD showed heterogeneous and diffuse FABP5 expression in atypical cells of all layers of the epidermis. This study is the first to investigate the role of FABP5 in premalignant skin lesions. The unique immunohistochemical localization of the FABP5 can be a helpful diagnostic marker, and altered fatty acid metabolism may be the key in understanding the different pathophysiology of AK and BD.
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