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O6-甲基鸟嘌呤-DNA甲基转移酶启动子高甲基化在结直肠癌发生中的作用

O6-methylguanine-DNA methyltransferase promoter hypermethylation in colorectal carcinogenesis.

作者信息

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

机构信息

DKBW, University of Modena and Reggio Emilia, Modena, Italy.

出版信息

Oncol Rep. 2007 Jun;17(6):1421-7.

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.

摘要

已有报道称,在结直肠肿瘤中存在表观遗传改变,这些改变可能补充或在某些情况下易导致基因改变,如K-ras突变。我们在用亚硫酸氢钠转化并通过甲基化特异性PCR进行DNA扩增后,检测了CDKN2A和O6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)基因的启动子甲基化状态。此外,我们在正常结直肠黏膜、异常隐窝灶(ACF,早期癌前病变)和癌组织中搜索了K-ras癌基因第12和13密码子的G到A转换。CDKN2A高甲基化在ACF中是罕见事件(26例中有2例,7.7%)。相反,在所检测的正常黏膜中(12个样本中有3个,25%)、26个ACF中的14个(53.8%)以及9个癌组织中的7个(77.8%)发现了MGMT高甲基化。K-ras突变在6个ACF(23%)和3个癌组织(33.3%)中明显存在,大多与MGMT启动子高甲基化相关。这些发现有力地支持了表观遗传机制在结直肠癌发生早期阶段起重要作用这一假说。

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