Disclosures: The following people have nothing to disclose: Mingyue

Zhu, Junli Guo, Hua Xia, Xieju Xie, Mengsen Li Fibroblast growth factor 4 (FGFR4), a receptor tyrosine kinase, is active and overexpressed in many cancers including cholan-giocarcinoma. We have confirmed expression of FGFR4 and its ligand, fibroblast growth factor 19 (FGF19), in a panel of cholangiocarcinoma cells. Our preliminary studies have identified this signaling pathway as pro-proliferative and anti-apop-totic, and inhibition of FGFR signaling (with click here a small molecule inhibitor, PD173074) decreases proliferation and sensitizes cells to TRAIL-induced apoptosis. Treatment of cholangiocarci-noma cells with FGF19 leads to an increase in FGFR4 levels as well as cleavage of a novel R4-ICD (receptor 4 – intracellular domain), which is lost with FGFR inhibition. We have also identified cell cycle regulation of FGFR4, including R4-ICD. Upon release from G1 block, synchronized cells express higher

levels FGFR4 and R4-ICD at 4 and 8 hours after re-entry into the cell cycle, corresponding to S-phase. In addition, cells treated with PD173074 show cell cycle arrest at G0/G1, and have slower progression through the cell cycle than vehicle treated cells; indicating that FGFR4 is regulated by the cell cycle and can modulate progression through the cell cycle. To begin to evaluate the role of FGFR4 in the cell cycle, we visualized FGFR4 during different cell phases. During G0/G1 and S-phase, FGFR4 is localized Luminespib to the plasma membrane and cytoplasm. In mitotic cells, FGFR4 is decreased

at the plasma membrane and cytoplasm, and is localized at the mitotic spindles. Co-staining with alpha-tubulin and FGFR4 indicates co-localization at the mitotic spindle during mitosis and 上海皓元 at the mid-body during cytokinesis. Preliminary pre-clinical studies in a rat model of cholangiocarcinoma show ∼55% reduction in tumor weight when FGFR signaling is inhibited. Increased cell death was confirmed in tumors exposed to the FGFR inhibitor via TUNEL assay. We are currently evaluating how FGFR4 is cleaved and its role in mitosis at the mitotic spindle. We conclude that FGFR4 signaling is a pro-survival mechanism in cholangiocar-cinoma and have identified a novel function of FGFR4 in cell cycle regulation. Disclosures: The following people have nothing to disclose: Ashley M. Mohr, Mary A. Smith, Sathish Kumar Natarajan, Cody J. Wehrkamp, Carol A. Casey, Justin L. Mott “
“I was flattered when Keith Lindor asked me to contribute to the “Master’s Perspective” series, especially when I saw the list of prior contributors, a “Who’s-Who” of hepatology. It was reassuring that I was friends with all the prior contributors, collaborated with many of them, and was critically mentored by one of them (Alan Hofmann) (Fig. 1A).