<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yoshioka Y</submitter><funding>Core Research for Evolutional Science and Technology</funding><funding>Japan Agency for Medical Research and Development</funding><funding>Center of Innovation Program</funding><funding>Japan Society for the Promotion of Science</funding><pagination>3498-3509</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9530877</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>113(10)</volume><pubmed_abstract>Early detection of pancreatic ductal adenocarcinoma (PDAC) is essential for improving patient survival rates, and noninvasive biomarkers are urgently required to identify patients who are eligible for curative surgery. Here, we examined extracellular vesicles (EVs) from the serum of PDAC patients to determine their ability to detect early-stage disease. EV-associated proteins purified by ultracentrifugation and affinity columns underwent proteomic analysis to identify novel PDAC markers G protein-coupled receptor class C group 5 member C (GPRC5C) and epidermal growth factor receptor pathway substrate 8 (EPS8). To verify the potency of GPRC5C- or EPS8-positive EVs as PDAC biomarkers, we analyzed EVs from PDAC patient blood samples using ultracentrifugation in two different cohorts (a total </pubmed_abstract><journal>Cancer science</journal><pubmed_title>Circulating cancer-associated extracellular vesicles as early detection and recurrence biomarkers for pancreatic cancer.</pubmed_title><pmcid>PMC9530877</pmcid><funding_grant_id>JP20cm0106402</funding_grant_id><funding_grant_id>JPMJCR19H1</funding_grant_id><funding_grant_id>15H05791</funding_grant_id><pubmed_authors>Mori M</pubmed_authors><pubmed_authors>Itoi T</pubmed_authors><pubmed_authors>Eguchi H</pubmed_authors><pubmed_authors>Nakatsura T</pubmed_authors><pubmed_authors>Doki Y</pubmed_authors><pubmed_authors>Kuroda M</pubmed_authors><pubmed_authors>Saito K</pubmed_authors><pubmed_authors>Ishii H</pubmed_authors><pubmed_authors>Ochiya T</pubmed_authors><pubmed_authors>Shimomura M</pubmed_authors><pubmed_authors>Yoshioka Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Circulating cancer-associated extracellular vesicles as early detection and recurrence biomarkers for pancreatic cancer.</name><description>Early detection of pancreatic ductal adenocarcinoma (PDAC) is essential for improving patient survival rates, and noninvasive biomarkers are urgently required to identify patients who are eligible for curative surgery. Here, we examined extracellular vesicles (EVs) from the serum of PDAC patients to determine their ability to detect early-stage disease. EV-associated proteins purified by ultracentrifugation and affinity columns underwent proteomic analysis to identify novel PDAC markers G protein-coupled receptor class C group 5 member C (GPRC5C) and epidermal growth factor receptor pathway substrate 8 (EPS8). To verify the potency of GPRC5C- or EPS8-positive EVs as PDAC biomarkers, we analyzed EVs from PDAC patient blood samples using ultracentrifugation in two different cohorts (a total </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-04T23:20:14.54Z</modification><creation>2025-04-04T23:20:14.54Z</creation></dates><accession>S-EPMC9530877</accession><cross_references><pubmed>35848896</pubmed><doi>10.1111/cas.15500</doi></cross_references></HashMap>