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10.1038/s41598-017-11914-6 http://scihub22266oqcxt.onion/10.1038/s41598-017-11914-6 C5597577!5597577 !28904399     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28904399 &cmd=llinks): Failed to open stream: HTTP request failed! 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Semaphorin 3?C drives epithelial-to-mesenchymal transition, invasiveness, and stem-like characteristics in prostate cells |pdf=|usr=}}{{28904399 }} gab.com Text Semaphorin 3 C drives epithelial-to-mesenchymal transition, invasiveness, and stem-like characteristics in prostate cells JO: Sci Rep http://www.kidney.de/pget.php?&tw=1&pmid=28904399 #FOAvip Prostate cancer (PCa) is among the most commonly-occurring cancers worldwide and a leader in cancer-related deaths. Local non-invasive PCa is highly treatable but limited treatment options exist for those with locally-advanced and metastatic forms of the disease underscoring the need to identify mechanisms mediating PCa progression. The semaphorins are a large grouping of membrane-associated or secreted signalling proteins whose normal roles reside in embryogenesis and neuronal development. In this context, semaphorins help establish chemotactic gradients and direct cell movement. Various semaphorin family members have been found to be up- and down-regulated in a number of cancers. One family member, Semaphorin 3?C (SEMA3C), has been implicated in prostate, breast, ovarian, gastric, lung, and pancreatic cancer as well as glioblastoma. Given SEMA3C's roles in development and its augmented expression in PCa, we hypothesized that SEMA3C promotes epithelial-to-mesenchymal transition (EMT) and stem-like phenotypes in prostate cells. In the present study we show that ectopic expression of SEMA3C in RWPE-1 promotes the upregulation of EMT and stem markers, heightened sphere-formation, and cell plasticity. In addition, we show that SEMA3C promotes migration and invasion in vitro and cell dissemination in vivo. Twit Text FOAVip Semaphorin 3 C drives epithelial-to-mesenchymal transition, invasiveness, and stem-like characteristics in prostate cells ????Sci Rep http://www.kidney.de/pget.php?&tw=1&pmid=28904399 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28904399 #FOAvip English Wikipedia <ref>{{Cite pmid|28904399 }}</ref> Semaphorin 3?C drives epithelial-to-mesenchymal transition, invasiveness, and stem-like characteristics in prostate cells #MMPMID28904399 Tam KJ ; Hui DHF ; Lee WW ; Dong M ; Tombe T ; Jiao IZF ; Khosravi S ; Takeuchi A ; Peacock JW ; Ivanova L ; Moskalev I ; Gleave ME ; Buttyan R ; Cox ME ; Ong CJ Sci Rep 2017[Sep]; 7 (1 ): 11501 PMID28904399 show ga Prostate cancer (PCa) is among the most commonly-occurring cancers worldwide and a leader in cancer-related deaths. Local non-invasive PCa is highly treatable but limited treatment options exist for those with locally-advanced and metastatic forms of the disease underscoring the need to identify mechanisms mediating PCa progression. The semaphorins are a large grouping of membrane-associated or secreted signalling proteins whose normal roles reside in embryogenesis and neuronal development. In this context, semaphorins help establish chemotactic gradients and direct cell movement. Various semaphorin family members have been found to be up- and down-regulated in a number of cancers. One family member, Semaphorin 3?C (SEMA3C), has been implicated in prostate, breast, ovarian, gastric, lung, and pancreatic cancer as well as glioblastoma. Given SEMA3C's roles in development and its augmented expression in PCa, we hypothesized that SEMA3C promotes epithelial-to-mesenchymal transition (EMT) and stem-like phenotypes in prostate cells. In the present study we show that ectopic expression of SEMA3C in RWPE-1 promotes the upregulation of EMT and stem markers, heightened sphere-formation, and cell plasticity. In addition, we show that SEMA3C promotes migration and invasion in vitro and cell dissemination in vivo. |Animals [MESH] |Biomarkers [MESH] |Cell Line, Tumor [MESH] |Cell Movement [MESH] |Cell Proliferation [MESH] |Disease Models, Animal [MESH] |Epithelial-Mesenchymal Transition/*genetics [MESH] |Gene Expression [MESH] |Heterografts [MESH] |Humans [MESH] |Immunophenotyping [MESH] |Male [MESH] |Mice [MESH] |Neoplasm Invasiveness [MESH] |Neoplastic Stem Cells/*metabolism [MESH] |Prostatic Neoplasms/*genetics/*metabolism/pathology [MESH]Semaphorin 3?C drives epithelial-to-mesenchymal transition, invasivene(epmc).pdf DeepDyve Pubget Overpricing