Ontology highlight
ABSTRACT: Background
Most mismatch repair-deficient (MMRd) colorectal cancer (CRC) cases arise sporadically, associated with somatic MLH1 methylation, whereas approximately 20% have germline mismatch repair pathogenic variants causing Lynch syndrome (LS). Universal screening of incident CRC uses presence of MLH1 methylation in MMRd tumors to exclude sporadic cases from germline testing for LS. However, this overlooks rare cases with constitutional MLH1 methylation (epimutation), a poorly recognized mechanism for LS. We aimed to assess the frequency and age distribution of constitutional MLH1 methylation among incident CRC cases with MMRd, MLH1-methylated tumors.Methods
In retrospective population-based studies, we selected all CRC cases with MMRd, MLH1-methylated tumors, regardless o
SUBMITTER: Hitchins MP
PROVIDER: S-EPMC11578100 | biostudies-literature | 2023 Jul
REPOSITORIES: biostudies-literature