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Notch Intracellular Domain Expression in Various Skin Fibroproliferative Diseases
Annals of Dermatology ; : 332-337, 2014.
Artigo em Inglês | WPRIM | ID: wpr-58741
ABSTRACT

BACKGROUND:

The effects of the Notch signaling pathway in fibroproliferative skin diseases have not been fully elucidated.

OBJECTIVE:

The aim of this study was to investigate the expression of activated Notch signaling molecules in various skin fibroproliferative diseases.

METHODS:

Immunohistochemical analysis of Notch intracellular domain (NICD) expression in keloid, hypertrophic scar, morphea, dermatofibroma, and normal control skin specimens was performed, and the clinical characteristics of patients with various skin fibroproliferative diseases were analyzed.

RESULTS:

NICD was highly expressed in fibroblasts of keloids and moderately to highly expressed in hypertrophic scars and dermatofibromas, whereas low or no expression was detected in the fibroblasts of normal skin specimens and morpheas. NICD was constitutively expressed in keratinocytes, endothelial cells, and immune cells in normal skin specimens.

CONCLUSION:

NICD was significantly expressed in human fibroproliferative skin disorders, especially keloids, suggesting that an activated Notch signaling pathway is involved in the pathogenesis of skin fibrosis.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Esclerodermia Localizada / Pele / Dermatopatias / Fibrose / Queratinócitos / Cicatriz Hipertrófica / Histiocitoma Fibroso Benigno / Células Endoteliais / Receptores Notch / Fibroblastos Limite: Humanos Idioma: Inglês Revista: Annals of Dermatology Ano de publicação: 2014 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Esclerodermia Localizada / Pele / Dermatopatias / Fibrose / Queratinócitos / Cicatriz Hipertrófica / Histiocitoma Fibroso Benigno / Células Endoteliais / Receptores Notch / Fibroblastos Limite: Humanos Idioma: Inglês Revista: Annals of Dermatology Ano de publicação: 2014 Tipo de documento: Artigo