<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>109(8)</volume><submitter>Warneke VS</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>We investigated the expression of members of the epithelial cell adhesion molecule (EpCAM) signalling pathway in gastric cancer (GC) testing the following hypotheses: are these molecules expressed in GC and are they putatively involved in GC biology.&lt;h4>Methods&lt;/h4>The study cohort consisted of 482 patients. The following members of the EpCAM signalling pathway were analysed by immunohistochemistry and were correlated with various clinico-pathological patient characteristics: extracellular domain of EpCAM (EpEX), intracellular domain of EpCAM (EpICD), E-cadherin, β-catenin, presenilin-2 (PSEN2), and ADAM17.&lt;h4>Results&lt;/h4>All members of the EpCAM signalling pathway were differentially expressed in GC. The expression correlated significantly with tumour type (EpEX, EpICD,</pubmed_abstract><journal>British journal of cancer</journal><pagination>2217-27</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3798952</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Members of the EpCAM signalling pathway are expressed in gastric cancer tissue and are correlated with patient prognosis.</pubmed_title><pmcid>PMC3798952</pmcid><pubmed_authors>Ebert MP</pubmed_authors><pubmed_authors>Behrens HM</pubmed_authors><pubmed_authors>Warneke VS</pubmed_authors><pubmed_authors>Rocken C</pubmed_authors><pubmed_authors>Haag J</pubmed_authors><pubmed_authors>Kruger S</pubmed_authors><pubmed_authors>Simon E</pubmed_authors><pubmed_authors>Mathiak M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Members of the EpCAM signalling pathway are expressed in gastric cancer tissue and are correlated with patient prognosis.</name><description>&lt;h4>Background&lt;/h4>We investigated the expression of members of the epithelial cell adhesion molecule (EpCAM) signalling pathway in gastric cancer (GC) testing the following hypotheses: are these molecules expressed in GC and are they putatively involved in GC biology.&lt;h4>Methods&lt;/h4>The study cohort consisted of 482 patients. The following members of the EpCAM signalling pathway were analysed by immunohistochemistry and were correlated with various clinico-pathological patient characteristics: extracellular domain of EpCAM (EpEX), intracellular domain of EpCAM (EpICD), E-cadherin, β-catenin, presenilin-2 (PSEN2), and ADAM17.&lt;h4>Results&lt;/h4>All members of the EpCAM signalling pathway were differentially expressed in GC. The expression correlated significantly with tumour type (EpEX, EpICD,</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Oct</publication><modification>2025-04-04T19:30:08.392Z</modification><creation>2019-03-27T01:17:16Z</creation></dates><accession>S-EPMC3798952</accession><cross_references><pubmed>24008668</pubmed><doi>10.1038/bjc.2013.536</doi></cross_references></HashMap>