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BRAF突变与年轻患者结直肠癌中的CpG岛甲基化表型相关。

BRAF mutation is associated with the CpG island methylator phenotype in colorectal cancer from young patients.

作者信息

Ang Pei Woon, Li Wei Qi, Soong Richie, Iacopetta Barry

机构信息

School of Surgery M507, University of Western Australia, 35 Stirling Hwy, Nedlands 6009, Australia.

出版信息

Cancer Lett. 2009 Jan 18;273(2):221-4. doi: 10.1016/j.canlet.2008.08.001. Epub 2008 Sep 7.

Abstract

This study investigated the relationship between BRAF mutation, the CpG island methylator phenotype (CIMP+) and APC methylation in colorectal cancer (CRC) from young patients. The V600E BRAF mutation was found in 7% of cases and was strongly associated with the tumour features of proximal site, advanced stage and poor histological grade. More than half (53%) the tumours with BRAF mutation were also CIMP+ as evaluated by a standard panel of markers, compared to only 4% of tumours with wildtype BRAF (P<0.0001). In contrast to CIMP+, APC methylation was inversely correlated with BRAF mutation (P=0.02). BRAF mutation and CIMP+ are therefore likely to be involved in an alternate, albeit rare, pathway to APC inactivation during the development of CRC in younger patients.

摘要

本研究调查了年轻患者结直肠癌(CRC)中BRAF突变、CpG岛甲基化表型(CIMP+)与APC甲基化之间的关系。在7%的病例中发现了V600E BRAF突变,且其与肿瘤近端部位、晚期及低组织学分级的特征密切相关。根据一组标准标志物评估,超过一半(53%)携带BRAF突变的肿瘤也是CIMP+,而野生型BRAF肿瘤中这一比例仅为4%(P<0.0001)。与CIMP+相反,APC甲基化与BRAF突变呈负相关(P=0.02)。因此,在年轻患者CRC发生过程中,BRAF突变和CIMP+可能参与了一条虽罕见但与APC失活不同的途径。

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