Fornaro Lorenzo, Vivaldi Caterina, Caparello Chiara, Musettini Gianna, Baldini Editta, Masi Gianluca, Falcone Alfredo
Unit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Istituto Toscano Tumori, Via Roma 67, 56126 Pisa, Italy,
Unit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy, 2Unit of Oncology, Department of Oncology, Azienda USL2, Lucca, Italy.
Front Biosci (Elite Ed). 2016 Jan 1;8(1):170-80. doi: 10.2741/E758.
Epigenetic mechanisms are involved in gastrointestinal (GI) cancer pathogenesis. Insights into the molecular basis of GI carcinogenesis led to the identification of different epigenetic pathways and signatures that may play a role as therapeutic targets in metastatic colorectal cancer (mCRC) and non-colorectal GI tumors. Among these alterations, O6-methylguanine DNA methyltransferase (MGMT) gene promoter methylation is the most investigated biomarker and seems to be an early and frequent event, at least in CRC. Loss of expression of MGMT as a result of gene promoter methylation has been associated with interesting activity of alkylating agents in mCRC. However, the optimal methods for the definition of the MGMT status and additional predictive factors beyond MGMT in GI malignancies are lacking. Here we review the current role of MGMT methylation and other epigenetic alterations as potential treatment targets in GI tumors.
表观遗传机制参与胃肠道(GI)癌的发病过程。对GI癌发生分子基础的深入了解,促成了不同表观遗传途径和特征的识别,这些途径和特征可能作为转移性结直肠癌(mCRC)和非结直肠GI肿瘤的治疗靶点发挥作用。在这些改变中,O6-甲基鸟嘌呤DNA甲基转移酶(MGMT)基因启动子甲基化是研究最多的生物标志物,并且似乎是一个早期且常见的事件,至少在结直肠癌中如此。由于基因启动子甲基化导致的MGMT表达缺失,与mCRC中烷化剂的有趣活性相关。然而,目前缺乏用于定义MGMT状态的最佳方法以及GI恶性肿瘤中除MGMT之外的其他预测因素。在此,我们综述了MGMT甲基化和其他表观遗传改变作为GI肿瘤潜在治疗靶点的当前作用。