<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shibayama Y</submitter><funding>NIDDK NIH HHS</funding><pagination>8854</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4352858</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5</volume><pubmed_abstract>Although Wnt/β-catenin signaling is known to be aberrantly activated in PDAC, mutations of CTNNB1, APC or other pathway components are rare in this tumor type, suggesting alternative mechanisms for Wnt/β-catenin activation. Recent studies have implicated the (pro)renin receptor ((P)RR) is related to the Wnt/β-catenin signaling pathway. We therefore investigated the possible role of (P)RR in pancreatic carcinogenesis. Plasma s(P)RR levels were significantly (P &lt; 0.0001) higher in patients with PDAC than in healthy matched controls. We also identified aberrant expression of (P)RR in premalignant PanIN and PDAC lesions and all the PDAC cell lines examined. Inhibiting (P)RR with an siRNA attenuated activation of Wnt/β-catenin signaling pathway and reduced the proliferative ability of PDAC cell</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>(Pro)renin receptor is crucial for Wnt/β-catenin-dependent genesis of pancreatic ductal adenocarcinoma.</pubmed_title><pmcid>PMC4352858</pmcid><funding_grant_id>R01 DK072408</funding_grant_id><pubmed_authors>Fujimori T</pubmed_authors><pubmed_authors>Kobori H</pubmed_authors><pubmed_authors>Shibayama Y</pubmed_authors><pubmed_authors>Masaki T</pubmed_authors><pubmed_authors>Kitada K</pubmed_authors><pubmed_authors>Nishiyama A</pubmed_authors><pubmed_authors>Nguyen G</pubmed_authors><pubmed_authors>Ichihara A</pubmed_authors><pubmed_authors>Totsune K</pubmed_authors><pubmed_authors>Nakano D</pubmed_authors><pubmed_authors>Kohno M</pubmed_authors><pubmed_authors>Suzuki Y</pubmed_authors><pubmed_authors>Yachida S</pubmed_authors><pubmed_authors>Hirose T</pubmed_authors></additional><is_claimable>false</is_claimable><name>(Pro)renin receptor is crucial for Wnt/β-catenin-dependent genesis of pancreatic ductal adenocarcinoma.</name><description>Although Wnt/β-catenin signaling is known to be aberrantly activated in PDAC, mutations of CTNNB1, APC or other pathway components are rare in this tumor type, suggesting alternative mechanisms for Wnt/β-catenin activation. Recent studies have implicated the (pro)renin receptor ((P)RR) is related to the Wnt/β-catenin signaling pathway. We therefore investigated the possible role of (P)RR in pancreatic carcinogenesis. Plasma s(P)RR levels were significantly (P &lt; 0.0001) higher in patients with PDAC than in healthy matched controls. We also identified aberrant expression of (P)RR in premalignant PanIN and PDAC lesions and all the PDAC cell lines examined. Inhibiting (P)RR with an siRNA attenuated activation of Wnt/β-catenin signaling pathway and reduced the proliferative ability of PDAC cell</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Mar</publication><modification>2025-04-18T15:30:26.047Z</modification><creation>2019-03-27T01:47:47Z</creation></dates><accession>S-EPMC4352858</accession><cross_references><pubmed>25747895</pubmed><doi>10.1038/srep08854</doi></cross_references></HashMap>