Ang Pei Woon, Li Wei Qi, Soong Richie, Iacopetta Barry
School of Surgery M507, University of Western Australia, 35 Stirling Hwy, Nedlands 6009, Australia.
Cancer Lett. 2009 Jan 18;273(2):221-4. doi: 10.1016/j.canlet.2008.08.001. Epub 2008 Sep 7.
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.
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。