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               <dc:title>Beta-catenin cleavage enhances transcriptional activation</dc:title>
               <dc:creator>Goretsky, Tatiana</dc:creator>
               <dc:creator>Bradford, Emily M.</dc:creator>
               <dc:creator>Ye, Qing</dc:creator>
               <dc:creator>Lamping, Olivia F.</dc:creator>
               <dc:creator>Vanagunas, Tomas</dc:creator>
               <dc:creator>Moyer, Mary Pat</dc:creator>
               <dc:creator>Keller, Patrick C.</dc:creator>
               <dc:creator>Sinh, Preetika</dc:creator>
               <dc:creator>Llovet i Bayer, Josep Maria</dc:creator>
               <dc:creator>Gao, Tianyan</dc:creator>
               <dc:creator>She, Qing-Bai</dc:creator>
               <dc:creator>Li, Linheng</dc:creator>
               <dc:creator>Barrett, Terrence A.</dc:creator>
               <dc:subject>Colitis</dc:subject>
               <dc:subject>Càncer colorectal</dc:subject>
               <dc:subject>Inflamació</dc:subject>
               <dc:subject>Colitis</dc:subject>
               <dc:subject>Colorectal cancer</dc:subject>
               <dc:subject>Inflammation</dc:subject>
               <dc:description>Nuclear activation of Wnt/β-catenin signaling is required for cell proliferation in inflammation and cancer. Studies from our group indicate that β-catenin activation in colitis and colorectal cancer (CRC) correlates with increased nuclear levels of β-catenin phosphorylated at serine 552 (pβ-Cat552). Biochemical analysis of nuclear extracts from cancer biopsies revealed the existence of low molecular weight (LMW) pβ-Cat552, increased to the exclusion of full size (FS) forms of β-catenin. LMW β-catenin lacks both termini, leaving residues in the armadillo repeat intact. Further experiments showed that TCF4 predominantly binds LMW pβ-Cat552 in the nucleus of inflamed and cancerous cells. Nuclear chromatin bound localization of LMW pβ-Cat552 was blocked in cells by inhibition of proteasomal chymotrypsin-like activity but not by other protease inhibitors. K48 polyubiquitinated FS and LMW β-catenin were increased by treatment with bortezomib. Overexpressed in vitro double truncated β-catenin increased transcriptional activity, cell proliferation and growth of tumor xenografts compared to FS β-catenin. Serine 552-> alanin substitution abrogated K48 polyubiquitination, β-catenin nuclear translocation and tumor xenograft growth. These data suggest that a novel proteasome-dependent posttranslational modification of β-catenin enhances transcriptional activation. Discovery of this pathway may be helpful in the development of diagnostic and therapeutic tools in colitis and cancer.</dc:description>
               <dc:date>2018-11-28T11:24:44Z</dc:date>
               <dc:date>2018-11-28T11:24:44Z</dc:date>
               <dc:date>2018-01-12</dc:date>
               <dc:date>2018-11-28T11:24:45Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>Reproducció del document publicat a: https://doi.org/10.1038/s41598-017-18421-8</dc:relation>
               <dc:relation>Scientific Reports, 2018, vol. 8, num. 1, p. 671</dc:relation>
               <dc:relation>https://doi.org/10.1038/s41598-017-18421-8</dc:relation>
               <dc:rights>cc-by (c) Goretsky, Tatiana et al., 2018</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by/3.0/es</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Nature Publishing Group</dc:publisher>
               <dc:source>Articles publicats en revistes (Medicina)</dc:source>
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