Silencing of Kangai 1 C-terminal interacting tetraspanin suppresses progression of cholangiocarcinoma
Highlights: • KITENIN is expressed in murine and human cholangiocarcinoma (CC). • Knockdown of KITENIN reduced proliferation, migration, invasion and colony formation in CC cells. • Silencing of KITENIN inhibited the expression of epithelial-mesenchymal transition markers. • Targeting of KITENIN might function as a new therapeutic strategy against CC. Cholangiocarcinoma (CC) is the second most common primary hepatic malignancy. CC treatment options are very limited especially for patients with distant metastasis. Kangai 1 C-terminal interacting tetraspanin (KITENIN) is highly expressed in numerous cancers, but the role of KITENIN in CC remains unknown. Here, we have investigated for the first time the function of KITENIN in human CC cell lines (TFK-1, SZ-1), tissues and a CC mouse model (Alb-Cre/LSL-KRAS{sup G12D}/p53{sup L/L}). KITENIN was expressed in 92.2% of human CC tissues, in murine CC samples and also in human CC cell lines. Knockdown of KITENIN by small interfering RNA (siRNA) effectively reduced proliferation, migration, invasion and colony formation in both intra- and extra-hepatic CC cells. The expression of epithelial-mesenchymal transition (EMT) markers like N-cadherin, Vimentin, Snail and Slug were suppressed in KITENIN knockdown CC cells. Our results indicate that KITENIN is crucial for cholangiocarcinogenesis and it might become a potential therapeutic target for human CC treatment.