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10.18632/oncotarget.7985 http://scihub22266oqcxt.onion/10.18632/oncotarget.7985 C5008324!5008324 !26967563     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26967563 &cmd=llinks): Failed to open stream: HTTP request failed! 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Phosphatase of regenerating liver-3 inhibits invasiveness and proliferation in non-small cell lung cancer by regulating the epithelial-mesenchymal transition |pdf=|usr=}}{{26967563 }} gab.com Text Phosphatase of regenerating liver-3 inhibits invasiveness and proliferation in non-small cell lung cancer by regulating the epithelial-mesenchymal transition JO: Oncotarget http://www.kidney.de/pget.php?&tw=1&pmid=26967563 #FOAvip Phosphatase of regenerating liver-3 (PRL-3) has been reported to be associated with colon and gastric cancer metastasis. However, the role and function of PRL-3 in human non-small cell lung cancer cells is unknown. Our studies showed that the expression of PRL-3mRNA and protein are higher in less invasive human lung adenocarcinoma cells than in highly invasive cell lines. Ectopic expression of PRL-3 reduced cell capacity for anchorage-dependent growth, anchorage-independent growth, migration, and invasion in vitro, as well as tumorigenesis in vivo. Conversely, catalytic (C104S) and prenylation-site (C170S) mutants enhanced cell invasion. Microarray profiling of PRL-3 transfectants revealed the pathways potentially involving PRL-3, including the epithelial-mesenchymal transition (EMT), extracellular matrix remodeling, and the WNT signaling pathway. Furthermore, we demonstrated that increased PRL-3 reduced Slug and enhanced E-cadherin gene expression through the AKT/GSK3?/?-catenin pathway. In conclusion, our data suggest that PRL-3 might play a tumor suppressor role in lung cancer, distinct from other cancers, by inhibiting EMT-related pathways. Twit Text FOAVip Phosphatase of regenerating liver-3 inhibits invasiveness and proliferation in non-small cell lung cancer by regulating the epithelial-mesenchymal transition ????Oncotarget http://www.kidney.de/pget.php?&tw=1&pmid=26967563 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26967563 #FOAvip English Wikipedia <ref>{{Cite pmid|26967563 }}</ref> Phosphatase of regenerating liver-3 inhibits invasiveness and proliferation in non-small cell lung cancer by regulating the epithelial-mesenchymal transition #MMPMID26967563 Lin SY ; Lee YX ; Yu SL ; Chang GC ; Chen JJ Oncotarget 2016[Apr]; 7 (16 ): 21799-811 PMID26967563 show ga Phosphatase of regenerating liver-3 (PRL-3) has been reported to be associated with colon and gastric cancer metastasis. However, the role and function of PRL-3 in human non-small cell lung cancer cells is unknown. Our studies showed that the expression of PRL-3mRNA and protein are higher in less invasive human lung adenocarcinoma cells than in highly invasive cell lines. Ectopic expression of PRL-3 reduced cell capacity for anchorage-dependent growth, anchorage-independent growth, migration, and invasion in vitro, as well as tumorigenesis in vivo. Conversely, catalytic (C104S) and prenylation-site (C170S) mutants enhanced cell invasion. Microarray profiling of PRL-3 transfectants revealed the pathways potentially involving PRL-3, including the epithelial-mesenchymal transition (EMT), extracellular matrix remodeling, and the WNT signaling pathway. Furthermore, we demonstrated that increased PRL-3 reduced Slug and enhanced E-cadherin gene expression through the AKT/GSK3?/?-catenin pathway. In conclusion, our data suggest that PRL-3 might play a tumor suppressor role in lung cancer, distinct from other cancers, by inhibiting EMT-related pathways. |A549 Cells [MESH] |Animals [MESH] |Cadherins/genetics/metabolism [MESH] |Carcinoma, Non-Small-Cell Lung/*genetics/metabolism/pathology [MESH] |Cell Line, Tumor [MESH] |Cell Movement/genetics [MESH] |Cell Proliferation/*genetics [MESH] |Epithelial-Mesenchymal Transition/*genetics [MESH] |Gene Expression Profiling/methods [MESH] |Gene Expression Regulation, Neoplastic [MESH] |Humans [MESH] |Kaplan-Meier Estimate [MESH] |Lung Neoplasms/*genetics/metabolism/pathology [MESH] |Mice, Nude [MESH] |Mutation [MESH] |Neoplasm Invasiveness [MESH] |Neoplasm Proteins/*genetics/metabolism [MESH] |Protein Tyrosine Phosphatases/*genetics/metabolism [MESH] |Signal Transduction/genetics [MESH]Phosphatase of regenerating liver-3 inhibits invasiveness and prolifer(epmc).pdf DeepDyve Pubget Overpricing