O6-methylguanine-DNA methyltransferase promoter hypermethylation in colorectal carcinogenesis

被引:0
|
作者
Menigatti, Mirco
Pedroni, Monica
Verrone, Anna Maria
Borghi, Francesca
Scarselli, Alessandra
Benatti, Piero
Losi, Lorena
Di Gregorio, Carmela
Schar, Primo
Marra, Giancarlo
De Leon, Maurizio Ponz
Roncucci, Luca
机构
[1] Univ Basel, DKBW, Dept Biol Clin Sci, Ctr Biomed, CH-4058 Basel, Switzerland
[2] Univ Modena, Dept Internal Med, I-41100 Modena, Italy
[3] Univ Modena, Dept Pathol, I-41100 Modena, Italy
[4] Univ Modena, Div Med Oncol, Dept Hematol & Oncol, I-41100 Modena, Italy
[5] Osped Carpi, Dept Pathol, Carpi, Italy
[6] Univ Zurich, Inst Mol Canc Res, Zurich, Switzerland
关键词
aberrant Crypt foci; O-6-methylguanine-DNA methyltransferase promoter hypermethylation; colorectal cancer; colorectal carcinogenesis; K-ras mutation;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 O-6-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.
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收藏
页码:1421 / 1427
页数:7
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