<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Geisler A</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>IBB Business Team GmbH program ProValid</funding><pagination>11224</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11508574</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(20)</volume><pubmed_abstract>Pancreatic cancer is one of the deadliest cancers globally, with limited success from existing therapies, including chemotherapies and immunotherapies like checkpoint inhibitors for patients with advanced pancreatic ductal adenocarcinoma (PDAC). A promising new approach is the use of oncolytic viruses (OV), a form of immunotherapy that has been demonstrated clinical effectiveness in various cancers. Here we investigated the potential of the oncolytic coxsackievirus B3 strain (CVB3) PD-H as a new treatment for pancreatic cancer. In vitro, PD-H exhibited robust replication, as measured by plaque assays, and potent lytic activity, as assessed by XTT assays, in most pancreatic tumor cell lines, outperforming two other coxsackievirus strains tested, H3N-375/1TS and CVA21. Thus, H3N-375/1TS show</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Oncolytic Coxsackievirus B3 Strain PD-H Is Effective Against a Broad Spectrum of Pancreatic Cancer Cell Lines and Induces a Growth Delay in Pancreatic KPC Cell Tumors In Vivo.</pubmed_title><pmcid>PMC11508574</pmcid><funding_grant_id>536819681</funding_grant_id><funding_grant_id>VAL121/2023</funding_grant_id><pubmed_authors>Fechner H</pubmed_authors><pubmed_authors>Elsner L</pubmed_authors><pubmed_authors>Klopfleisch R</pubmed_authors><pubmed_authors>Geisler A</pubmed_authors><pubmed_authors>Dieringer B</pubmed_authors><pubmed_authors>Kurreck J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Oncolytic Coxsackievirus B3 Strain PD-H Is Effective Against a Broad Spectrum of Pancreatic Cancer Cell Lines and Induces a Growth Delay in Pancreatic KPC Cell Tumors In Vivo.</name><description>Pancreatic cancer is one of the deadliest cancers globally, with limited success from existing therapies, including chemotherapies and immunotherapies like checkpoint inhibitors for patients with advanced pancreatic ductal adenocarcinoma (PDAC). A promising new approach is the use of oncolytic viruses (OV), a form of immunotherapy that has been demonstrated clinical effectiveness in various cancers. Here we investigated the potential of the oncolytic coxsackievirus B3 strain (CVB3) PD-H as a new treatment for pancreatic cancer. In vitro, PD-H exhibited robust replication, as measured by plaque assays, and potent lytic activity, as assessed by XTT assays, in most pancreatic tumor cell lines, outperforming two other coxsackievirus strains tested, H3N-375/1TS and CVA21. Thus, H3N-375/1TS show</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2025-04-18T14:58:17.19Z</modification><creation>2025-04-07T01:20:34.659Z</creation></dates><accession>S-EPMC11508574</accession><cross_references><pubmed>39457005</pubmed><doi>10.3390/ijms252011224</doi></cross_references></HashMap>