Conclusion: Together, these findings identify a novel mechanism mediating the oncogenic function of SULF2 in HCC that includes GPC3-mediated activation of Wnt signaling via the Wnt3a/glycogen synthase kinase 3 beta axis. (HEPATOLOGY 2010;) BSA, bovine serum albumin; DAPI, 4′,6-diamidino-2-phenylindole dihydrochloride; FGF, fibroblast growth factor; GFP, green fluorescent protein; GPC3, glypican 3; GSK3β, glycogen synthase kinase 3 beta; HCC, hepatocellular carcinoma; HPF, high-power field; HS, heparan sulfate; HSGAG, heparan sulfate glycosaminoglycan; HSPG, heparan

sulfate proteoglycan; IP, immunoprecipitation; LEF, lymphoid enhancer-binding factor; mRNA, messenger RNA; PBS, phosphate-buffered saline; shRNA, short hairpin RNA; SULF2, sulfatase 2; TCF, T cell factor; TUNEL, terminal deoxynucleotidyl learn more transferase–mediated deoxyuridine triphosphate nick-end labeling. Hepatocellular carcinoma (HCC) is the third most frequent cause of cancer death worldwide.1 The survival of HCC patients is poor, and only 10% to 20% of HCCs are detected at an early enough stage for potentially curative therapy. Locoregional therapies are usually palliative, and

there are limited options this website for chemotherapy. Therefore, new agents are needed for the effective treatment of the majority of HCCs.2 The Wnt/Frizzled/β-catenin pathway is activated in approximately 50% of HCCs. Wnt ligands (Wnt3, Wnt3a, Wnt4, and Wnt5a) and Frizzled receptors (Frizzled 3, Frizzled 6, and Frizzled 7) have been implicated in the development of HCC, and up to 95% of HCCs show potential Wnt/Frizzled activating events.3-5 The Wnt/β-catenin pathway is regulated by heparan sulfate proteoglycans (HSPGs), which modulate cell surface signaling by acting as coreceptors or storage sites for Wnt proteins. HSPGs consist of a MCE公司 protein core to which heparan

sulfate glycosaminoglycan (HSGAG) chains are attached; these are variably sulfated at the 2-O, 3-O, and 6-O positions of their component disaccharides. Glypicans are cell surface–anchored HSPGs that regulate the activity of Wnts.6, 7 In particular, glypican 3 (GPC3) is highly overexpressed in HCCs and is being developed as a target for HCC therapy.8, 9 Wnt3a has been shown to mediate the GPC3-induced growth of HCCs via the canonical Wnt/β-catenin pathway.5, 10 Sulfated HSGAG chains of GPC3 and other HSPGs are potential substrates for desulfation at the 6-O position by human sulfatase 2 (SULF2). The sulfation state of HSGAGs is critical for growth factor binding; hence, SULF2 may regulate tumor growth by releasing growth factors from HSGAG storage sites at the cell surface and in the extracellular matrix and thus may increase the local concentration of growth factors available to bind to cell surface receptors and enhance cell signaling.