<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Blaine-Sauer S</submitter><funding>Mr. Eric Becker and his family</funding><funding>Dr. Jamie Koufman</funding><funding>Medical College of Wisconsin Department of Otolaryngology and Communication Sciences</funding><pagination>6765</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10095080</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(7)</volume><pubmed_abstract>Gastroesophageal reflux disease (GERD) significantly impacts patient quality of life and is a major risk factor for the development of Barrett's esophagus (BE) and esophageal adenocarcinoma (EAC). Proton pump inhibitors (PPIs) are the standard-of-care for GERD and are among the most prescribed drugs in the world, but do not protect against nonacid components of reflux such as pepsin, or prevent reflux-associated carcinogenesis. We recently identified an HIV protease inhibitor amprenavir that inhibits pepsin and demonstrated the antireflux therapeutic potential of its prodrug fosamprenavir in a mouse model of laryngopharyngeal reflux. In this study, we assessed the capacity of amprenavir to protect against esophageal epithelial barrier disruption in vitro and related molecular events, E-cad</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>The Protease Inhibitor Amprenavir Protects against Pepsin-Induced Esophageal Epithelial Barrier Disruption and Cancer-Associated Changes.</pubmed_title><pmcid>PMC10095080</pmcid><funding_grant_id>N/A</funding_grant_id><funding_grant_id>Donation</funding_grant_id><pubmed_authors>Yan K</pubmed_authors><pubmed_authors>Blaine-Sauer S</pubmed_authors><pubmed_authors>Samuels TL</pubmed_authors><pubmed_authors>Johnston N</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Protease Inhibitor Amprenavir Protects against Pepsin-Induced Esophageal Epithelial Barrier Disruption and Cancer-Associated Changes.</name><description>Gastroesophageal reflux disease (GERD) significantly impacts patient quality of life and is a major risk factor for the development of Barrett's esophagus (BE) and esophageal adenocarcinoma (EAC). Proton pump inhibitors (PPIs) are the standard-of-care for GERD and are among the most prescribed drugs in the world, but do not protect against nonacid components of reflux such as pepsin, or prevent reflux-associated carcinogenesis. We recently identified an HIV protease inhibitor amprenavir that inhibits pepsin and demonstrated the antireflux therapeutic potential of its prodrug fosamprenavir in a mouse model of laryngopharyngeal reflux. In this study, we assessed the capacity of amprenavir to protect against esophageal epithelial barrier disruption in vitro and related molecular events, E-cad</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-07-10T03:08:13.159Z</modification><creation>2025-04-04T12:15:41.3Z</creation></dates><accession>S-EPMC10095080</accession><cross_references><pubmed>37047737</pubmed><doi>10.3390/ijms24076765</doi></cross_references></HashMap>