<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Grutzmeier SE</submitter><funding>Tømrermester Jørgen Holm og Hustru Elisa f. Hansens Mindelegats</funding><funding>Arvd Nilssons Fond</funding><funding>Dagmar Marshalls Fond</funding><funding>Lægeforeningens Forskningsfond</funding><funding>Danish Cancer Society</funding><pagination>3677</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10377599</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(14)</volume><pubmed_abstract>Cancer-associated fibroblasts (CAFs) have been shown to impact the chemosensitivity of patient-derived tumor organoids (PDTOs). However, the published literature comparing PDTO response to clinical outcome does not include CAFs in the models. Here, a co-culture model was created using PDTOs and CAFs derived from endoscopic ultrasound-guided fine-needle biopsies (EUS-FNBs) for potential use in drug screening applications. Co-cultures were established, and growth was compared to monocultures using image metrics and a commercially available assay. We were able to establish and expand validated malignant PDTOs from 19.2% of adenocarcinomas from EUS-FNBs. CAFs could be established from 25% of the samples. The viability of PDTOs in the mixed cell co-culture could be isolated using image metrics.</pubmed_abstract><journal>Cancers</journal><pubmed_title>Validation of a Novel EUS-FNB-Derived Organoid Co-Culture System for Drug Screening in Patients with Pancreatic Cancer.</pubmed_title><pmcid>PMC10377599</pmcid><funding_grant_id>2019-3780/40</funding_grant_id><funding_grant_id>F-10215-00-86</funding_grant_id><funding_grant_id>R322-A17350</funding_grant_id><funding_grant_id>F-19215-00-65.</funding_grant_id><funding_grant_id>21081</funding_grant_id><pubmed_authors>Grossjohann H</pubmed_authors><pubmed_authors>Chiranth D</pubmed_authors><pubmed_authors>Klausen P</pubmed_authors><pubmed_authors>Grutzmeier SE</pubmed_authors><pubmed_authors>Kovacevic B</pubmed_authors><pubmed_authors>Hasselby JP</pubmed_authors><pubmed_authors>Karstensen JG</pubmed_authors><pubmed_authors>Rift CV</pubmed_authors><pubmed_authors>Hogdall E</pubmed_authors><pubmed_authors>Holmstrom MO</pubmed_authors><pubmed_authors>Melchior LC</pubmed_authors><pubmed_authors>Vilmann P</pubmed_authors><pubmed_authors>Hansen CP</pubmed_authors><pubmed_authors>Brink L</pubmed_authors><pubmed_authors>Toxværd A</pubmed_authors><pubmed_authors>Hassan H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Validation of a Novel EUS-FNB-Derived Organoid Co-Culture System for Drug Screening in Patients with Pancreatic Cancer.</name><description>Cancer-associated fibroblasts (CAFs) have been shown to impact the chemosensitivity of patient-derived tumor organoids (PDTOs). However, the published literature comparing PDTO response to clinical outcome does not include CAFs in the models. Here, a co-culture model was created using PDTOs and CAFs derived from endoscopic ultrasound-guided fine-needle biopsies (EUS-FNBs) for potential use in drug screening applications. Co-cultures were established, and growth was compared to monocultures using image metrics and a commercially available assay. We were able to establish and expand validated malignant PDTOs from 19.2% of adenocarcinomas from EUS-FNBs. CAFs could be established from 25% of the samples. The viability of PDTOs in the mixed cell co-culture could be isolated using image metrics.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jul</publication><modification>2025-04-05T00:23:09.857Z</modification><creation>2025-04-05T00:23:09.857Z</creation></dates><accession>S-EPMC10377599</accession><cross_references><pubmed>37509338</pubmed><doi>10.3390/cancers15143677</doi></cross_references></HashMap>