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Paired bladder cancer and adjacent tissue samples (102) and normal bladder tissue samples (106) were obtained. Bladder cancer cell lines (T24, 5637, <jats:styled-content style=\"fixed-case\">RT<\/jats:styled-content>4, 253J and J82) were selected and assigned to blank, negative control (<jats:styled-content style=\"fixed-case\">NC<\/jats:styled-content>), <jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>\u2010\u03b2, thrombospondin\u20101 (<jats:styled-content style=\"fixed-case\">TSP<\/jats:styled-content>\u20101), <jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>\u2010\u03b21+ <jats:styled-content style=\"fixed-case\">TSP<\/jats:styled-content>\u20101, <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73\u2010si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\u20101, <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73\u2010si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\u20102, <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73\u2010si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\u20101+ <jats:styled-content style=\"fixed-case\">TSP<\/jats:styled-content>\u20101, <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73\u2010si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\u20101+ pc<jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73, <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>1\u2010si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>1\u2010si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content> + <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73\u2010si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\u20101 groups. Expressions of <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73, <jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>\u2010\u03b21, Smad2, p\u2010Smad2, E\u2010cadherin and vimentin were detected using <jats:styled-content style=\"fixed-case\">RT<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">qPCR<\/jats:styled-content> and Western blotting. Cell proliferation, migration and invasion were determined using <jats:styled-content style=\"fixed-case\">MTT<\/jats:styled-content> assay, scratch testing and Transwell assay, respectively. Compared with the blank and <jats:styled-content style=\"fixed-case\">NC<\/jats:styled-content> groups, levels of <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73, <jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>\u2010\u03b21, Smad2, p\u2010Smad2, N\u2010cadherin and vimentin decreased, and levels of <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>1 and E\u2010cadherin increased in the <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73\u2010si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\u20101 and <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73\u2010si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\u20102 groups, while the opposite results were observed in the <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>1 si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> TGF<\/jats:styled-content>\u2010\u03b2, <jats:styled-content style=\"fixed-case\">TSP<\/jats:styled-content>\u20101 and <jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>\u2010\u03b2 + <jats:styled-content style=\"fixed-case\">TSP<\/jats:styled-content>\u20101 groups. Cell proliferation, migration and invasion notably decreased in the <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73\u2010si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\u20101 and <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73\u2010si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\u20102 groups in comparison with the blank and <jats:styled-content style=\"fixed-case\">NC<\/jats:styled-content> groups, while in the <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>1 si<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> TGF<\/jats:styled-content>\u2010\u03b2, <jats:styled-content style=\"fixed-case\">TSP<\/jats:styled-content>\u20101 and <jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>\u2010\u03b2 + <jats:styled-content style=\"fixed-case\">TSP<\/jats:styled-content>\u20101 groups, cell migration, invasion and proliferation showed the reduction after the <jats:styled-content style=\"fixed-case\">EMT<\/jats:styled-content>. These results suggest that <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>73 promotes bladder cancer invasion and metastasis by inducing the <jats:styled-content style=\"fixed-case\">EMT<\/jats:styled-content> through down\u2010regulating <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>1 levels and activating the <jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>\u2010\u03b21\/Smad2 signalling pathway.<\/jats:p>","DOI":"10.1111\/jcmm.13442","type":"journal-article","created":{"date-parts":[[2018,1,19]],"date-time":"2018-01-19T05:09:18Z","timestamp":1516338558000},"page":"1650-1665","source":"Crossref","is-referenced-by-count":25,"title":["<scp>GP<\/scp>73 promotes invasion and metastasis of bladder cancer by regulating the epithelial\u2013mesenchymal transition through the <scp>TGF<\/scp>\u2010\u03b21\/Smad2 signalling 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