<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(11)</volume><submitter>Tanabe S</submitter><pubmed_abstract>&lt;h4>Aim&lt;/h4>To investigate β-catenin (CTNNB1) signaling in cancer and stem cells, the gene expression and pathway were analyzed using bioinformatics.&lt;h4>Methods&lt;/h4>The expression of the catenin β 1 (&lt;i>CTNNB1&lt;/i>) gene, which codes for β-catenin, was analyzed in mesenchymal stem cells (MSCs) and gastric cancer (GC) cells. Beta-catenin signaling and the mutation of related proteins were also analyzed using the cBioPortal for Cancer Genomics and HOMology modeling of Complex Structure (HOMCOS) databases.&lt;h4>Results&lt;/h4>The expression of the &lt;i>CTNNB1&lt;/i> gene was up-regulated in GC cells compared to MSCs. The expression of EPH receptor A8 (EPHA8), synovial sarcoma translocation chromosome 18 (SS18), interactor of little elongation complex ELL subunit 1 (ICE1), patched 1 (PTCH1), mutS homolog</pubmed_abstract><journal>World journal of stem cells</journal><pagination>384-395</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5120243</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Gene expression and pathway analysis of &lt;i>CTNNB1&lt;/i> in cancer and stem cells.</pubmed_title><pmcid>PMC5120243</pmcid><pubmed_authors>Kawabata T</pubmed_authors><pubmed_authors>Aoyagi K</pubmed_authors><pubmed_authors>Sasaki H</pubmed_authors><pubmed_authors>Yokozaki H</pubmed_authors><pubmed_authors>Tanabe S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Gene expression and pathway analysis of &lt;i>CTNNB1&lt;/i> in cancer and stem cells.</name><description>&lt;h4>Aim&lt;/h4>To investigate β-catenin (CTNNB1) signaling in cancer and stem cells, the gene expression and pathway were analyzed using bioinformatics.&lt;h4>Methods&lt;/h4>The expression of the catenin β 1 (&lt;i>CTNNB1&lt;/i>) gene, which codes for β-catenin, was analyzed in mesenchymal stem cells (MSCs) and gastric cancer (GC) cells. Beta-catenin signaling and the mutation of related proteins were also analyzed using the cBioPortal for Cancer Genomics and HOMology modeling of Complex Structure (HOMCOS) databases.&lt;h4>Results&lt;/h4>The expression of the &lt;i>CTNNB1&lt;/i> gene was up-regulated in GC cells compared to MSCs. The expression of EPH receptor A8 (EPHA8), synovial sarcoma translocation chromosome 18 (SS18), interactor of little elongation complex ELL subunit 1 (ICE1), patched 1 (PTCH1), mutS homolog</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Nov</publication><modification>2025-04-22T21:18:05.476Z</modification><creation>2019-03-27T02:29:36Z</creation></dates><accession>S-EPMC5120243</accession><cross_references><pubmed>27928465</pubmed><doi>10.4252/wjsc.v8.i11.384</doi></cross_references></HashMap>