bgr-catenin expression in pilomatrixomas. Relationship with bgr-catenin gene mutations and comparison with bgr-catenin expression in normal hair follicles

Authors: Moreno-Bueno G.; Gamallo C.1; Pérez-Gallego L.2; Contreras F.3; Palacios J.

Source: British Journal of Dermatology, Volume 145, Number 4, October 2001 , pp. 576-581(6)

Publisher: Blackwell Publishing

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Abstract:

Background bgr-catenin functions in signal transduction in the Wnt signalling pathway, which has recently been implicated in hair follicle (HF) morphogenesis. bgr-catenin gene mutations affecting exon 3 have been reported in a high percentage of human pilomatrixomas. However, the expression pattern of bgr-catenin in human HFs and pilomatrixomas has not been reported.

Objectives To analyse immunohistochemically the expression pattern of bgr-catenin in normal anagen HFs and in 40 human pilomatrixomas.

Methods In 11 of these tumours we also studied exon 3 bgr-catenin gene mutations by polymerase chain reaction and direct sequencing. As these mutations have been related to a replication error (RER) phenotype in other tumour types, we explored whether or not this association also occurs in pilomatrixomas.

Results bgr-catenin was expressed in the cell membranes of the outer and inner root sheaths and in matrix cells located at the base and periphery of the HF bulb. However, central matrix cells that differentiate into cortical cells, cortical and cuticular cells expressed bgr-catenin in the nucleus, suggesting a role in signal transduction. In addition, some fibroblasts of the dermal papilla also showed nuclear expression of bgr-catenin. All 40 analysed pilomatrixomas showed intense nuclear and cytoplasmic bgr-catenin expression in proliferating matrix (basaloid) cells. In areas of maturation, transitional cells mainly showed cytoplasmic and membranous expression of bgr-catenin, while only a few cells retained nuclear expression. Shadow or ghost cells did not show bgr-catenin expression. Three of 11 tumours (26%) had bgr-catenin mutations. All three had the same heterozygote mis-sense mutation: a G to T change affecting the first nucleotide at codon 32 (D32Y). None of the 11 tumours studied had a positive RER phenotype.

Conclusions Present and previous studies suggest that the Wnt/bgr-catenin/Tcf-Lef pathway is activated in normal matrix cells of the HF to induce differentiation to the hair shaft. Additionally, the bgr-catenin mutation in matrix cells of the HF stabilizes bgr-catenin protein, which translocates into the nucleus, where it activates of gene transcription together with lymphoid enhancer factor-1 producing pilomatrixoma. These mutations occur without an underlying defect in DNA mismatch repair.

Keywords: bgr-catenin; hair follicle; pilomatrixoma

Document Type: Research article

DOI: 10.1046/j.1365-2133.2001.04455.x

Affiliations: 1: Servicio de Anatominodot´a Patológica, Hospital Universitario La Princesa, Madrid, Spain ´a Patológica, Hospital Universitario La Princesa, Madrid, Spain "> 2: Servicio de Anatominodot´a Patológica, Hospital Rio Hortega, Valladolid, Spain ´a Patológica, Hospital Rio Hortega, Valladolid, Spain "> 3: Departamento de Anatominodot´a Patológica, Hospital Universitario La Paz, Madrid, Spain´a Patológica, Hospital Universitario La Paz, Madrid, Spain">

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