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http://purl.uniprot.org/citations/28209511http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28209511http://www.w3.org/2000/01/rdf-schema#comment"Heparanase-1/syndecan-1 axis plays critical roles in tumorigenesis and development. The main mechanism includes heparanase-1 (HPA-1) degrades the heparan sulfate chain of syndecan-1 (SDC-1), and the following shedding of heparan sulfate from tumor cell releases and activates SDC-1 sequestered growth factors. However, the significance of Heparanase-1/syndecan-1 axis and its effects on the microenvironment of lymphatic metastasis in hepatocellular carcinogenesis (HCC) procession have not been reported. Herein, we found that HPA-1 could degrade the heparan sulfate on hepatocarcinoma cell surface. Importantly, HPA-1-induced shedding of heparan sulfate chain from SDC-1 facilitated the release of vascular endothelial growth factor C (VEGF-C) from SDC-1/VEGF-C complex into the medium of hepatocarcinoma cell. Further studies indicated that VEGF-C secretion from hepatocarcinoma cell promoted lymphatic endothelial cell growth through activating extracellular signal-regulated kinase (ERK) signaling. Taken together, this study reveals a novel existence of Heparanase-1/syndecan-1 axis in hepatocarcinoma cell and its roles in the cross-talking with the microenvironment of lymphatic metastasis."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.org/dc/terms/identifier"doi:10.1016/j.bbrc.2017.02.060"xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Hong Y."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Jiang L."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Jiang Y."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Lv H."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Zhang Q."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Wang S."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Yu S."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Zhang J."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Zhang H."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Zhang J.'"xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Ou G."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Xia R."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/author"Ju W."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/name"Biochem Biophys Res Commun"xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/pages"432-439"xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/title"Heparanase-1-induced shedding of heparan sulfate from syndecan-1 in hepatocarcinoma cell facilitates lymphatic endothelial cell proliferation via VEGF-C/ERK pathway."xsd:string
http://purl.uniprot.org/citations/28209511http://purl.uniprot.org/core/volume"485"xsd:string
http://purl.uniprot.org/citations/28209511http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28209511
http://purl.uniprot.org/citations/28209511http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/28209511
http://purl.uniprot.org/uniprot/#_P97953-mappedCitation-28209511http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28209511
http://purl.uniprot.org/uniprot/#_Q6YGZ1-mappedCitation-28209511http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28209511