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DOI 10.1111/j.1365-2613.2011.00779.x

Медицинская библиотека · International journal of experimental pathology · 2011

Gene expression profiling in male genital lichen sclerosus.

Edmonds Emma, Barton Geraint, Buisson Sandrine, Francis Nick, Gotch Frances, Game Laurence, Haddad Munther, Dinneen Michael, Bunker Chris

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Male genital lichen sclerosus (MGLSc) has a bimodal distribution in boys and men. It is associated with squamous cell carcinoma (SCC). The pathogenesis of MGLSc is unknown. HPV and autoimmune mechanisms have been mooted. Anti extracellular matrix protein (ECM)1 antibodies have been identified in women with GLSc. The gene expression pattern of LSc is unknown. Using DNA microarrays we studied differences in gene expression in healthy and diseased prepuces obtained at circumcision in adult males with MGLSc (n = 4), paediatric LSc (n = 2) and normal healthy paediatric foreskin (n = 4). In adult samples 51 genes with significantly increased expression and 87 genes with significantly reduced expression were identified; paediatric samples revealed 190 genes with significantly increased expression and 148 genes with significantly reduced expression. Concordance of expression profiles between adult and paediatric samples indicates the same disease process. Functional analysis revealed increased expression in the adult and child MGSLc samples in the immune response/cellular defence gene ontology (GO) category and reduced expression in other categories including genes related to squamous cancer. No specific HPV, autoimmune or squamous carcinogenesis-associated gene expression patterns were found. ECM1 and CABLES1 expression were significantly reduced in paediatric and adult samples respectively.

Для цитирования: Edmonds Emma, Barton Geraint, Buisson Sandrine, Francis Nick, Gotch Frances, Game Laurence, Haddad Munther, Dinneen Michael, Bunker Chris. Gene expression profiling in male genital lichen sclerosus.. International journal of experimental pathology. 2011. DOI: 10.1111/j.1365-2613.2011.00779.x.

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