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O6-methylguanine-DNA methyltransferase promoter hypermethylation in colorectal carcinogenesis
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 110573
Author(s) Menigatti, Mirco; Pedroni, Monica; Verrone, Anna Maria; Borghi, Francesca; Scarselli, Alessandra; Benatti, Piero; Losi, Lorena; Di Gregorio, Carmela; Schär, Primo; Marra, Giancarlo; Ponz de Leon, Maurizio; Roncucci, Luca
Author(s) at UniBasel Schär, Primo Leo
Year 2007
Title O6-methylguanine-DNA methyltransferase promoter hypermethylation in colorectal carcinogenesis
Journal Oncology reports
Volume 17
Number 6
Pages / Article-Number 1421-7
Keywords aberrant Crypt foci, O-6-methylguanine-DNA methyltransferase promoter hypermethylation, colorectal cancer, colorectal carcinogenesis, K-ras mutation
Abstract

Epigenetic alterations have been reported in colorectal neoplasia which can either complement or in some cases be predisposed to genetic alterations such as K-ras mutations. We examined the promoter methylation status of the CDKN2A and O6-methylguanine-DNA methyltransferase (MGMT) genes, after sodium bisulfite conversion and DNA amplification with methylation specific PCR. Moreover, we searched for G to A transitions in codons 12 and 13 of the K-ras oncogene in normal colorectal mucosae, aberrant crypt foci (ACF, early premalignant lesions) and carcinomas. CDKN2A hypermethylation was an infrequent event in ACF (2 of 26, 7.7%). On the contrary, MGMT hypermethylation was found in the normal mucosae (3 of the 12 samples, 25%), in 14 of the 26 ACF (53.8%) and in 7 of the 9 (77.8%) carcinomas examined. K-ras mutations were evident in 6 ACF (23%) and in 3 carcinomas (33.3%), mostly associated with MGMT promoter hypermethylation. These findings strongly support the hypothesis that epigenetic mechanisms play an important role in the early steps of colorectal carcinogenesis.

Publisher D.A. Spandidos
ISSN/ISBN 1021-335X
edoc-URL http://edoc.unibas.ch/dok/A5253995
Full Text on edoc No
Digital Object Identifier DOI 10.3892/or.17.6.1421
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/17487400
ISI-Number WOS:000246774000021
Document type (ISI) Journal Article
 
   

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