<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chhoda A</submitter><funding>NCATS NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIH HHS</funding><pagination>28</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9942382</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Intraductal papillary mucinous neoplasms (IPMNs), a type of cystic pancreatic cancer (PC) precursors, are increasingly identified on cross-sectional imaging and present a significant diagnostic challenge. While surgical resection of IPMN-related advanced neoplasia, i.e., IPMN-related high-grade dysplasia or PC, is an essential early PC detection strategy, resection is not recommended for IPMN-low-grade dysplasia (LGD) due to minimal risk of carcinogenesis, and significant procedural risks. Based on their promising results in prior validation studies targeting early detection of classical PC, DNA hypermethylation-based markers may serve as a biomarker for malignant risk stratification of IPMNs. This study investigates our DNA methylation-based PC biomarker panel (ADAMTS1,</pubmed_abstract><journal>Clinical epigenetics</journal><pubmed_title>Utility of promoter hypermethylation in malignant risk stratification of intraductal papillary mucinous neoplasms.</pubmed_title><pmcid>PMC9942382</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>R01 CA185357</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><funding_grant_id>P30CA016359</funding_grant_id><pubmed_authors>Tan WY</pubmed_authors><pubmed_authors>Kunstman JW</pubmed_authors><pubmed_authors>Sailo B</pubmed_authors><pubmed_authors>Iacobuzio-Donahue C</pubmed_authors><pubmed_authors>Khatri R</pubmed_authors><pubmed_authors>Wolfgang CL</pubmed_authors><pubmed_authors>Ruzgar N</pubmed_authors><pubmed_authors>Tang H</pubmed_authors><pubmed_authors>Ying L</pubmed_authors><pubmed_authors>Salem RR</pubmed_authors><pubmed_authors>Mane S</pubmed_authors><pubmed_authors>Sharma A</pubmed_authors><pubmed_authors>Chhoda A</pubmed_authors><pubmed_authors>Narayanan A</pubmed_authors><pubmed_authors>De Kumar B</pubmed_authors><pubmed_authors>Wood LD</pubmed_authors><pubmed_authors>Farrell JJ</pubmed_authors><pubmed_authors>Ahuja N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Utility of promoter hypermethylation in malignant risk stratification of intraductal papillary mucinous neoplasms.</name><description>&lt;h4>Background&lt;/h4>Intraductal papillary mucinous neoplasms (IPMNs), a type of cystic pancreatic cancer (PC) precursors, are increasingly identified on cross-sectional imaging and present a significant diagnostic challenge. While surgical resection of IPMN-related advanced neoplasia, i.e., IPMN-related high-grade dysplasia or PC, is an essential early PC detection strategy, resection is not recommended for IPMN-low-grade dysplasia (LGD) due to minimal risk of carcinogenesis, and significant procedural risks. Based on their promising results in prior validation studies targeting early detection of classical PC, DNA hypermethylation-based markers may serve as a biomarker for malignant risk stratification of IPMNs. This study investigates our DNA methylation-based PC biomarker panel (ADAMTS1,</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-22T08:52:02.516Z</modification><creation>2025-02-18T22:55:02.029Z</creation></dates><accession>S-EPMC9942382</accession><cross_references><pubmed>36803844</pubmed><doi>10.1186/s13148-023-01429-5</doi></cross_references></HashMap>