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International Journal of Experimental Pathology
Article . 2011 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
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Gene expression profiling in male genital lichen sclerosus

Authors: Emma, Edmonds; Geraint, Barton; Sandrine, Buisson; Nick, Francis; Frances, Gotch; Laurence, Game; Munther, Haddad; +2 Authors

Gene expression profiling in male genital lichen sclerosus

Abstract

SummaryMale 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.

Keywords

Adult, Male, Extracellular Matrix Proteins, Skin Neoplasms, Gene Expression Profiling, Foreskin, Middle Aged, Phosphoproteins, Lichen Sclerosus et Atrophicus, Case-Control Studies, Child, Preschool, Cyclins, Carcinoma, Squamous Cell, Humans, Carrier Proteins, Child, Precancerous Conditions, Aged

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
45
Top 10%
Top 10%
Top 10%
bronze
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