Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/4243
Title: Immunohistochemical expression of ß-catenin, E-cadherin, cyclin D1 and c-myc in benign trichogenic tumors
Authors: Demirkan, Neşe Çallı
Bir, Ferda.
Erdem, O.
Düzcan, E.
Keywords: beta catenin
cyclin D1
Myc protein
uvomorulin
adolescent
adult
aged
article
benign tumor
cell membrane
cell nucleus
cellular distribution
child
controlled study
cytoplasm
female
histopathology
human
human tissue
immunohistochemistry
immunoreactivity
male
molecular biology
pilomatrixoma
protein depletion
protein expression
protein localization
sebaceous cyst
trichoepithelioma
tumor cell
Adolescent
Adult
Aged
Aged, 80 and over
beta Catenin
Cadherins
Child
Child, Preschool
Cyclins
Female
Hair Diseases
Humans
Immunohistochemistry
Male
Middle Aged
Neoplasm Proteins
Pilomatrixoma
Proto-Oncogene Proteins c-myc
Skin Neoplasms
Tumor Markers, Biological
Abstract: Background: ß-catenin gene mutations have been reported in vast majority of pilomatrixomas (PMXs). ß-catenin, a component of the adhesion molecules of the cytoskeleton, is degraded at the cytoplasm. Excess cytoplasmic ß-catenin enters into the nucleus and activates the transcription of several genes encoding c-myc, cyclin D1 and others. Sublocation of ß-catenin has been demonstrated by immunohistochemistry. The aim of this study was to determine the role of ß-catenin-related proteins in various benign trichogenic tumors. Methods: We investigated the expression of ß-catenin, E-cadherin, c-myc and cyclin D1 immunohistochemically, and the expression of these molecules were compared between two groups consisting of 12 PMXs and 12 other benign trichogenic tumors (OBTTs). Results: In PMX group, nuclear and/or cytoplasmic expression of ß-catenin was associated with a loss of membranous expression of E-cadherin (p = 0.002). In OBTT group, a membranous expression of E-cadherin and ß-catenin was observed, and there was a stronger nuclear immunoreactivity of cyclin D1 compared with PMX group (p = 0.006). Conclusions: In PMX, nuclear and/or cytoplasmic ß-catenin expression of tumoral cells is not related with ß-catenin-related gene expressions (c-myc or cyclin D1). The molecular behaviour of OBTTs is clearly different from that of PMXs in terms of to E-cadherin and ß-catenin expression. © Blackwell Munksgaard 2006.
URI: https://hdl.handle.net/11499/4243
https://doi.org/10.1111/j.1600-0560.2006.00636.x
ISSN: 0303-6987
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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