<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8</volume><submitter>Pham NA</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The pathogenesis of pancreatic ductal adenocarcinoma (PDAC) involves multi-stage development of molecular aberrations affecting signaling pathways that regulate cancer growth and progression. This study was performed to gain a better understanding of the abnormal signaling that occurs in PDAC compared with normal duct epithelia.&lt;h4>Methods&lt;/h4>We performed immunohistochemistry on a tissue microarray of 26 PDAC, 13 normal appearing adjacent pancreatic ductal epithelia, and 12 normal non-PDAC ducts. We compared the levels of 18 signaling proteins including growth factor receptors, tumor suppressors and 13 of their putative downstream phosphorylated (p-) signal transducers in PDAC to those in normal ductal epithelia.&lt;h4>Results&lt;/h4>The overall profiles of signaling protein </pubmed_abstract><journal>BMC cancer</journal><pagination>43</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2270852</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Immunohistochemical analysis of changes in signaling pathway activation downstream of growth factor receptors in pancreatic duct cell carcinogenesis.</pubmed_title><pmcid>PMC2270852</pmcid><pubmed_authors>Schwock J</pubmed_authors><pubmed_authors>Iakovlev V</pubmed_authors><pubmed_authors>Tsao MS</pubmed_authors><pubmed_authors>Pham NA</pubmed_authors><pubmed_authors>Hedley DW</pubmed_authors><pubmed_authors>Pond G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunohistochemical analysis of changes in signaling pathway activation downstream of growth factor receptors in pancreatic duct cell carcinogenesis.</name><description>&lt;h4>Background&lt;/h4>The pathogenesis of pancreatic ductal adenocarcinoma (PDAC) involves multi-stage development of molecular aberrations affecting signaling pathways that regulate cancer growth and progression. This study was performed to gain a better understanding of the abnormal signaling that occurs in PDAC compared with normal duct epithelia.&lt;h4>Methods&lt;/h4>We performed immunohistochemistry on a tissue microarray of 26 PDAC, 13 normal appearing adjacent pancreatic ductal epithelia, and 12 normal non-PDAC ducts. We compared the levels of 18 signaling proteins including growth factor receptors, tumor suppressors and 13 of their putative downstream phosphorylated (p-) signal transducers in PDAC to those in normal ductal epithelia.&lt;h4>Results&lt;/h4>The overall profiles of signaling protein </description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Feb</publication><modification>2026-03-16T16:40:01.882Z</modification><creation>2025-08-31T03:08:35.557Z</creation></dates><accession>S-EPMC2270852</accession><cross_references><pubmed>18254976</pubmed><doi>10.1186/1471-2407-8-43</doi></cross_references></HashMap>