Csepregi Antal, Röcken Christoph, Hoffmann Juliane, Gu Ping, Saliger Stephan, Müller Oliver, Schneider-Stock Regine, Kutzner Nadine, Roessner Albert, Malfertheiner Peter, Ebert Matthias P A
Department of Gastroenterology, Hepatology, and Infectious Diseases, Otto-von-Guericke University, Leipziger Strasse 44, 39120 Magdeburg, Germany.
J Cancer Res Clin Oncol. 2008 May;134(5):579-89. doi: 10.1007/s00432-007-0321-y. Epub 2007 Nov 1.
We investigated the impact of promoter methylation on APC protein expression in patients with hepatocellular carcinoma (HCC).
50 patients [HCC (n=19), liver metastasis (n=19), cholangiocellular cancer (n=7), and benign liver tumors (n=5)] were studied for methylation using Methylight analysis. APC mutation was investigated by protein truncation test and direct sequencing of genomic DNA. The protein expression was evaluated by immunohistochemistry and Western blot analysis.
The APC promoter was hypermethylated in 81.8% of non-cancerous liver tissue samples. All HCC samples and ten patients with liver metastasis (52.6%) exhibited APC promoter methylation. The degree of methylation was significantly higher in samples from HCC compared to the non-cancerous liver tissue samples (63.1% vs. 24.98%; p=0.001). The level of APC protein expression was significantly reduced in HCC samples compared to that of the corresponding non-tumor liver tissue (p<0.05).
Promoter methylation of the APC gene seems to be of significance in hepatocarcinogenesis and results in reduced protein expression in HCC. Interestingly, APC promoter methylation is also present in the vast majority of non-cancerous liver tissue whose (patho)physiological function remains unresolved.
我们研究了启动子甲基化对肝细胞癌(HCC)患者中APC蛋白表达的影响。
使用甲基化特异性荧光定量PCR分析对50例患者[肝细胞癌(n = 19)、肝转移癌(n = 19)、胆管细胞癌(n = 7)和良性肝肿瘤(n = 5)]进行甲基化研究。通过蛋白质截短试验和基因组DNA直接测序研究APC突变。通过免疫组织化学和蛋白质印迹分析评估蛋白质表达。
81.8%的非癌肝组织样本中APC启动子发生高甲基化。所有肝细胞癌样本和10例肝转移患者(52.6%)表现出APC启动子甲基化。与非癌肝组织样本相比,肝细胞癌样本中的甲基化程度显著更高(63.1%对24.98%;p = 0.001)。与相应的非肿瘤肝组织相比,肝细胞癌样本中APC蛋白表达水平显著降低(p < 0.05)。
APC基因的启动子甲基化似乎在肝癌发生中具有重要意义,并导致肝细胞癌中蛋白质表达减少。有趣的是,绝大多数非癌肝组织中也存在APC启动子甲基化,但其(病理)生理功能仍未明确。