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  3. PTCH promoter methylation at low level in sporadic basal cell carcinoma analysed by three different approaches

PTCH promoter methylation at low level in sporadic basal cell carcinoma analysed by three different approaches

Details
Publisher DOI
10.1111/j.1600-0625.2010.01120.x
PubMed ID
20849535
Abstract
Please cite this paper as: PTCH promoter methylation at low level in sporadic basal cell carcinoma analysed by three different approaches. Experimental Dermatology 2010. Abstract: Basal cell carcinoma (BCC) is the most common form of skin cancer. Mutations of the PTCH hallmark gene are detected in about 50-60% of BCCs, which raises the question whether other mechanisms such as promoter methylation can inactivate PTCH. Therefore, we performed methylation analysis of the PTCH promoter in a total of 56 BCCs. The sensitivity of three different methods, including direct bisulphite sequencing PCR, MethyLight and high-resolution melting (HRM), was applied and compared. We found that HRM analysis of DNA from fresh tissue [rather than formalin-fixed and paraffin-embedded tissue (FFPE)] was the most sensitive method to detect methylation. Low-level methylation of the PTCH promoter was detected in five out of 16 analysed BCCs (31%) on DNA from fresh tissue but only in two (13%) samples on short-time stored FFPE DNA from the very same tumors. In contrast, we were unable to detect methylation by HRM on long-time stored DNA in any of the remaining 40 BCC samples. Our data suggest that (i) HRM on DNA extracted from fresh tissue is the most sensitive method to detect methylation and (ii) methylation of the PTCH promoter may only play a minor role in BCC carcinogenesis.
Date Issued
2010
Publication Type
Article
Language(s)
en
Author(s)
Heitzer, Ellen
Bambach, Isabella
Dandachi, Nadia
Horn, Michael Peter
Universitätsinstitut für Immunologie  
Wolf, Peter
Additional Credits
Universitätsinstitut für Immunologie  
Journal
Experimental dermatology
Publisher
Blackwell
ISSN
0906-6705
Access(Rights)
metadata.only
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