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Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1
Authors:Goudie David R  D'Alessandro Mariella  Merriman Barry  Lee Hane  Szeverényi Ildikó  Avery Stuart  O'Connor Brian D  Nelson Stanley F  Coats Stephanie E  Stewart Arlene  Christie Lesley  Pichert Gabriella  Friedel Jean  Hayes Ian  Burrows Nigel  Whittaker Sean  Gerdes Anne-Marie  Broesby-Olsen Sigurd  Ferguson-Smith Malcolm A  Verma Chandra  Lunny Declan P  Reversade Bruno  Lane E Birgitte
Affiliation:Human Genetics Unit, University of Dundee College of Medicine, Dentistry and Nursing, Dundee, UK.
Abstract:Multiple self-healing squamous epithelioma (MSSE), also known as Ferguson-Smith disease (FSD), is an autosomal-dominant skin cancer condition characterized by multiple squamous-carcinoma-like locally invasive skin tumors that grow rapidly for a few weeks before spontaneously regressing, leaving scars. High-throughput genomic sequencing of a conservative estimate (24.2 Mb) of the disease locus on chromosome 9 using exon array capture identified independent mutations in TGFBR1 in three unrelated families. Subsequent dideoxy sequencing of TGFBR1 identified 11 distinct monoallelic mutations in 18 affected families, firmly establishing TGFBR1 as the causative gene. The nature of the sequence variants, which include mutations in the extracellular ligand-binding domain and a series of truncating mutations in the kinase domain, indicates a clear genotype-phenotype correlation between loss-of-function TGFBR1 mutations and MSSE. This distinguishes MSSE from the Marfan syndrome-related disorders in which missense mutations in TGFBR1 lead to developmental defects with vascular involvement but no reported predisposition to cancer.
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