Widespread microsatellite instability in sebaceous tumours of patients with the Muir-Torre syndrome

Ketty Peris, Mt Onorati, G Keller, F Magrini, P Donati, L Muscardin, H Höfler, S. Chimenti

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Muir-Torre syndrome (MTS) is an autosomal dominant disorder characterized by the presence of at least one sebaceous gland tumour and a minimum of one visceral malignant tumour. Recently, microsatellite instability (MSI) has been detected in the tumours of patients with MTS and germline mutations of the hMSH2 and hMLH1 mismatch repair genes have been detected in some patients with this syndrome. To determine if the tumours of patients with MTS have widespread genomic instability and whether loss of heterozygosity (LOH) in the chromosomal regions containing hMSH2 and hMLH1 is detectable, MSI and LOH were examined at 10 dinucleotide repeats on chromosomes 2p, 3p, 5q, 9p, 17p and 18q. Data were obtained from six sebaceous gland tumours and two adenocarcinomas of the colon from three patients of two Muir-Torre families. MSI was detected at more than half of the loci tested in all sebaceous tumours examined. In addition, there was LOH at D2S119 in one sebaceoma and one sebaceous carcinoma from one patient. The colon carcinomas from two patients showed MSI at five of the 10 loci analysed. These results show that widespread MSI is a feature of tumours in patients with MTS. In addition, the finding of LOH at D2S119, a marker located in the vicinity of hMSH2, in sebaceous tumours of one patient indicates that this gene may have a pathogenetic role in this patient.
Lingua originaleEnglish
pagine (da-a)356-360
Numero di pagine5
RivistaBritish Journal of Dermatology
Stato di pubblicazionePubblicato - 1997


  • Adult
  • Chromosome Deletion
  • Chromosomes, Human, Pair 2
  • Colonic Neoplasms
  • Female
  • Heterozygote
  • Humans
  • Male
  • Microsatellite Repeats
  • Middle Aged
  • Neoplasms, Multiple Primary
  • Neoplastic Syndromes, Hereditary
  • Pedigree
  • Sebaceous Gland Neoplasms


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