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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 Axø
Broesby-Olsen, Sigurd
Ferguson-Smith, Malcolm A
Verma, Chandra
Lunny, Declan P
Reversade, Bruno
Lane, E Birgitte
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 Axø
Broesby-Olsen, Sigurd
Ferguson-Smith, Malcolm A
Verma, Chandra
Lunny, Declan P
Reversade, Bruno
Lane, E Birgitte
Source :
Goudie , D R , D'Alessandro , M , Merriman , B , Lee , H , Szeverényi , I , Avery , S , O'Connor , B D , Nelson , S F , Coats , S E , Stewart , A , Christie , L , Pichert , G , Friedel , J , Hayes , I , Burrows , N , Whittaker , S , Gerdes , A-M A , Broesby-Olsen , S , Ferguson-Smith , M A , Verma , C , Lunny , D P , Reversade , B & Lane , E B 2011 , ' Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1 ' , Nature Genetics , vol. 43 , no. 4 , pp. 365-9 .
Publication Year :
2011

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.

Details

Database :
OAIster
Journal :
Goudie , D R , D'Alessandro , M , Merriman , B , Lee , H , Szeverényi , I , Avery , S , O'Connor , B D , Nelson , S F , Coats , S E , Stewart , A , Christie , L , Pichert , G , Friedel , J , Hayes , I , Burrows , N , Whittaker , S , Gerdes , A-M A , Broesby-Olsen , S , Ferguson-Smith , M A , Verma , C , Lunny , D P , Reversade , B & Lane , E B 2011 , ' Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1 ' , Nature Genetics , vol. 43 , no. 4 , pp. 365-9 .
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.ocn826493166
Document Type :
Electronic Resource