Experimental and Clinical Research Center, Charité Universitätsmedizin Berlin, and Max-Delbrück-Center for Molecular Medicine, Berlin, Germany.
Department of General-, Visceral- and Transplant Surgery, Charité Universitätsmedizin Berlin, Campus Virchow, Berlin, Germany.
Hepatology. 2015 Sep;62(3):841-50. doi: 10.1002/hep.27885. Epub 2015 Jun 26.
Curative treatment of intrahepatic cholangiocarcinoma (ICC) and hilar cholangiocarcinoma (Klatskin tumors) is limited to surgical resection or orthotopic liver transplantation. However, not all patients benefit from a surgical approach and suffer from early tumor recurrence. Response to chemotherapy is generally poor and, until today, no targeted therapy could be established. Metastasis-associated in colon cancer 1 (MACC1) is a recently discovered regulator of the hepatocyte growth factor (HGF)/Met/mitogen-activated protein kinase pathway, which induces proliferation, migration, and invasion in cell culture, as well as metastasis in mice. MACC1 expression shows a significant correlation with Met expression in colon cancer tissue and is highly prognostic for occurrence of distant metastasis and survival in colon cancer patients. Thus, we aimed to measure the expression of MACC1, Met, and HGF messenger RNA in microdissected tumor tissue and corresponding normal liver tissue of 156 patients with Klatskin tumors (n = 76) and ICC (n = 80) using real-time quantitative reverse-transcriptase polymerase chain reaction. We used immunohistochemical staining to validate the results. MACC1 expression in tumor tissue of both tumor entities was significantly higher than in corresponding normal liver tissue (P < 0.001). Klatskin tumor patients with a history of tumor recurrence had significantly higher MACC1 expression than those without tumor recurrence (P = 0.005). Uni- und multivariate survival analysis showed that Klatskin tumor patients with high MACC1 had a significantly shorter overall (OS) and disease-free survival (DFS; P = 0.001 and P < 0.001, respectively). The multivariate analysis confirmed MACC1 to be an independent factor for overall survival in Klatskin tumor patients (hazard ratio: 2.777; 95% confidence interval: 1.389-5.555; P = 0.004).
Our study identified MACC1 as a highly prognostic biomarker for OS and DFS in Klatskin tumor patients. MACC1 expression could become an important diagnostic tool and might be a candidate for targeted therapy.
检测微切割的肝内胆管细胞癌(ICC)和肝门部胆管癌(Klatskin 肿瘤)组织及相应的正常肝组织中转移相关基因 1(MACC1)、Met 和 HGFmRNA 的表达,探讨 MACC1 表达与 ICC 和 Klatskin 肿瘤临床病理特征的关系及其临床意义。
采用实时定量逆转录聚合酶链反应(RT-PCR)检测 156 例 Klatskin 肿瘤(n=76)和 ICC(n=80)患者肿瘤组织及相应的正常肝组织中 MACC1、Met 和 HGFmRNA 的表达,并通过免疫组化验证 RT-PCR 的结果。
ICC 和 Klatskin 肿瘤组织中 MACC1mRNA 的表达均明显高于相应的正常肝组织(P<0.001);肿瘤复发患者的 MACC1mRNA 表达明显高于无肿瘤复发患者(P=0.005);MACC1 高表达患者的总生存时间(OS)和无病生存时间(DFS)明显缩短(P<0.001,P=0.001);多因素分析显示,MACC1 是影响 Klatskin 肿瘤患者 OS 的独立预后因素(HR=2.777,95%CI:1.389~5.555,P=0.004)。
MACC1 是影响 ICC 和 Klatskin 肿瘤患者 OS 和 DFS 的独立预后因素,MACC1 有望成为判断 ICC 和 Klatskin 肿瘤患者预后的指标和潜在的治疗靶点。