Chen Jie, Röcken Christoph, Lofton-Day Cathy, Schulz Hans-Ulrich, Müller Oliver, Kutzner Nadine, Malfertheiner Peter, Ebert Matthias P A
Department of Gastroenterology, Hepatology and Infectious Diseases, Otto-von-Guericke University, Magdeburg, Germany.
Carcinogenesis. 2005 Jan;26(1):37-43. doi: 10.1093/carcin/bgh280. Epub 2004 Sep 16.
APC (adenomatous polyposis coli) promoter methylation has been linked to the early development of colorectal cancers. However, the role of APC methylation and its effect on protein expression in colon cancer metastasis is largely unknown. In this study, we investigated APC promoter methylation by Methylight analysis and analysed the APC protein levels by immunohistochemistry and western blot analysis in 24 liver metastasis and 39 primary colorectal cancers. Promoter methylation of the APC gene was found to be a frequent event in liver metastasis (10/24) and significantly more frequent compared with primary colorectal cancer (7/39, P = 0.047). APC methylation was not found in 14 matched normal colon tissues. APC protein was detected in the cytoplasm of primary and metastatic cancer cells and non-tumorous colon epithelium. By western blot analysis, APC protein levels were found to be decreased in primary tumour tissues compared with the normal colon mucosa. In contrast, APC protein levels were not decreased in the cancer cells that had metastasized to the liver. APC protein levels were independent of the presence of APC promoter methylation or gene mutations. In summary, APC promoter methylation is a frequent epigenetic alteration in colorectal cancer metastasis. However, we observed no significant association between APC promoter methylation or gene mutation and APC protein expression in colorectal metastasis. Therefore, metastatic cancer cells seem to harbour a heterogenous genetic and epigenetic background, in which cancer cells may exhibit APC promoter methylation that is independent of APC expression.
腺瘤性结肠息肉病(APC)启动子甲基化与结直肠癌的早期发展有关。然而,APC甲基化在结肠癌转移中的作用及其对蛋白质表达的影响在很大程度上尚不清楚。在本研究中,我们通过甲基化荧光定量分析研究了APC启动子甲基化,并通过免疫组织化学和蛋白质印迹分析对24例肝转移癌和39例原发性结直肠癌中的APC蛋白水平进行了分析。发现APC基因的启动子甲基化在肝转移癌中是常见事件(10/24),与原发性结直肠癌相比(7/39,P = 0.047)明显更常见。在14例匹配的正常结肠组织中未发现APC甲基化。在原发性和转移性癌细胞以及非肿瘤性结肠上皮细胞的细胞质中检测到了APC蛋白。通过蛋白质印迹分析发现,与正常结肠黏膜相比,原发性肿瘤组织中的APC蛋白水平降低。相反,转移至肝脏的癌细胞中的APC蛋白水平并未降低。APC蛋白水平与APC启动子甲基化或基因突变的存在无关。总之,APC启动子甲基化是结直肠癌转移中常见的表观遗传改变。然而,我们在结直肠癌转移中未观察到APC启动子甲基化或基因突变与APC蛋白表达之间存在显著关联。因此,转移性癌细胞似乎具有异质性的遗传和表观遗传背景,其中癌细胞可能表现出与APC表达无关的APC启动子甲基化。