<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Venis SM</submitter><funding>NCATS NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><pagination>3675-3685</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9175079</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(19)</volume><pubmed_abstract>A pancreatic acinus is a functional unit of the exocrine pancreas producing digest enzymes. Its pathobiology is crucial to pancreatic diseases including pancreatitis and pancreatic cancer, which can initiate from pancreatic acini. However, research on pancreatic acini has been significantly hampered due to the difficulty of culturing normal acinar cells &lt;i>in vitro&lt;/i>. In this study, an &lt;i>in vitro&lt;/i> model of the normal acinus, named pancreatic acinus-on-chip (PAC), is developed using reprogrammed pancreatic cancer cells. The developed model is a microfluidic platform with an epithelial duct and acinar sac geometry microfabricated by a newly developed two-step controlled "viscous-fingering" technique. In this model, human pancreatic cancer cells, Panc-1, reprogrammed to revert to the no</pubmed_abstract><journal>Lab on a chip</journal><pubmed_title>Engineering of a functional pancreatic acinus with reprogrammed cancer cells by induced &lt;i>PTF1a&lt;/i> expression.</pubmed_title><pmcid>PMC9175079</pmcid><funding_grant_id>R01 CA124586</funding_grant_id><funding_grant_id>R01 CA254110</funding_grant_id><funding_grant_id>P30 CA023168</funding_grant_id><funding_grant_id>P30 CA082709</funding_grant_id><funding_grant_id>R01 CA211098</funding_grant_id><funding_grant_id>UL1 TR002529</funding_grant_id><funding_grant_id>U01 HL143403</funding_grant_id><pubmed_authors>Moon HR</pubmed_authors><pubmed_authors>Konieczny SF</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Han B</pubmed_authors><pubmed_authors>Venis SM</pubmed_authors><pubmed_authors>Utturkar SM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Engineering of a functional pancreatic acinus with reprogrammed cancer cells by induced &lt;i>PTF1a&lt;/i> expression.</name><description>A pancreatic acinus is a functional unit of the exocrine pancreas producing digest enzymes. Its pathobiology is crucial to pancreatic diseases including pancreatitis and pancreatic cancer, which can initiate from pancreatic acini. However, research on pancreatic acini has been significantly hampered due to the difficulty of culturing normal acinar cells &lt;i>in vitro&lt;/i>. In this study, an &lt;i>in vitro&lt;/i> model of the normal acinus, named pancreatic acinus-on-chip (PAC), is developed using reprogrammed pancreatic cancer cells. The developed model is a microfluidic platform with an epithelial duct and acinar sac geometry microfabricated by a newly developed two-step controlled "viscous-fingering" technique. In this model, human pancreatic cancer cells, Panc-1, reprogrammed to revert to the no</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2026-05-09T20:13:16.736Z</modification><creation>2024-10-19T06:48:59.171Z</creation></dates><accession>S-EPMC9175079</accession><cross_references><pubmed>34581719</pubmed><doi>10.1039/d1lc00350j</doi></cross_references></HashMap>