<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Huang G</submitter><funding>National Cancer Institute Cancer Center</funding><funding>Brendon Colson Center for Pancreatic Care</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>411-422</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11560643</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>264(4)</volume><pubmed_abstract>The basement membrane (BM) is among the predominant microenvironmental factors of normal epithelia and of precancerous epithelial lesions. Evidence suggests that the BM functions not only as a barrier to tumour invasion but also as an active tumour-suppressing signalling substrate during premalignancy. However, the molecular foundations of such mechanisms have not been elucidated. Here we explore potential tumour-suppressing functions of the BM during precancer evolution, focusing on the expression and function of the extracellular matrix receptor dystroglycan in the pancreas and pancreatic disease. We show that the dystroglycan protein is highly expressed in the acinar compartment of the normal pancreas but lower in the ductal compartment. Moreover, there is a strong suppression of dystro</pubmed_abstract><journal>The Journal of pathology</journal><pubmed_title>Suppression of dystroglycan function accompanies pancreatic acinar-to-ductal metaplasia and favours dysplasia development.</pubmed_title><pmcid>PMC11560643</pmcid><funding_grant_id>P30CA069533</funding_grant_id><funding_grant_id>P30 CA069533</funding_grant_id><funding_grant_id>1U01 CA224012</funding_grant_id><funding_grant_id>U54 CA209988</funding_grant_id><funding_grant_id>U01 CA224012</funding_grant_id><funding_grant_id>U01 CA278923</funding_grant_id><funding_grant_id>U54CA209988</funding_grant_id><pubmed_authors>Chang YH</pubmed_authors><pubmed_authors>Lanciault C</pubmed_authors><pubmed_authors>MacPherson-Hawthorne K</pubmed_authors><pubmed_authors>Huang G</pubmed_authors><pubmed_authors>Ternes L</pubmed_authors><pubmed_authors>Sears RC</pubmed_authors><pubmed_authors>Muschler JL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Suppression of dystroglycan function accompanies pancreatic acinar-to-ductal metaplasia and favours dysplasia development.</name><description>The basement membrane (BM) is among the predominant microenvironmental factors of normal epithelia and of precancerous epithelial lesions. Evidence suggests that the BM functions not only as a barrier to tumour invasion but also as an active tumour-suppressing signalling substrate during premalignancy. However, the molecular foundations of such mechanisms have not been elucidated. Here we explore potential tumour-suppressing functions of the BM during precancer evolution, focusing on the expression and function of the extracellular matrix receptor dystroglycan in the pancreas and pancreatic disease. We show that the dystroglycan protein is highly expressed in the acinar compartment of the normal pancreas but lower in the ductal compartment. Moreover, there is a strong suppression of dystro</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2026-06-10T05:31:36.269Z</modification><creation>2026-06-10T03:07:42.68Z</creation></dates><accession>S-EPMC11560643</accession><cross_references><pubmed>39435649</pubmed><doi>10.1002/path.6356</doi></cross_references></HashMap>