Ming-Te Huang魏柏立劉俊仁Der-Zen LiuHuey-Chun HuangJane AnCheng-Chia WuChih-Hsiung WuYuan-Soon HoYi-Yuan YangYu-Jia Chang2026-06-052026-06-052011https://doi.org/10.1245/s10434-010-1163-4https://203.71.86.71/handle/123456789/49833Background Thrombomodulin (TM) is a key molecule mediating circulation homeostasis through its binding to thrombin. The TM–thrombin complex can activate protein C and thrombin-activatable fibrinolysis inhibitor to form a tight clot. In many cancer tissues, decrease of TM expression may correlate with cancer metastasis. However, the role of TM in hepatocellular carcinoma (HCC) progression is still unclear. Methods We characterized TM expression in HCC cells (HepJ5 and skHep-1 cells) using real-time polymerase chain reaction (PCR) and Western blotting. We then manipulated TM expression using both TM-specific short hairpin RNA (shRNA) and overexpressing it in HCC cells. Transwell migration assay was performed to monitor the migratory ability of HCC cells under different levels of TM expression. Results We found that TM was ectopically highly expressed in skHep-1 at both transcriptional and translational levels. After silencing TM expression in skHep-1 cells, we found that metastatic capability was dramatically increased. Conversely, overexpression of TM in HepJ5 cells decreased metastatic ability. We investigated the possible mechanism and found that decreased TM-mediated enhancement of cell migration was dependent on upregulation of ZEB1, a repressor of E-cadherin. Conclusions TM may be a modulator of cancer metastasis in HCC. Downregulation of TM expression may increase ZEB1 and decrease E-cadherin levels.醫學檢驗暨生物技術學系期刊論文article