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Metastasis‐associated in colon cancer 1 is an independent prognostic biomarker for survival in klatskin tumor patients

医学 结直肠癌 转移 克拉茨金瘤 肝内胆管癌 肝细胞生长因子 免疫组织化学 肿瘤科 内科学 癌症 病理 癌症研究 切除术 受体 外科
作者
Andri Lederer,Pia Herrmann,Daniel Seehofer,Manfred Dietel,Johann Pratschke,P. Schlag,Ulrike Stein
出处
期刊:Hepatology [Lippincott Williams & Wilkins]
卷期号:62 (3): 841-850 被引量:24
标识
DOI:10.1002/hep.27885
摘要

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). Conclusion: 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. (H epatology 2015;62:841–850)
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