Ontology highlight
ABSTRACT: Background
Metabolic dysfunction-associated steatohepatitis (MASH) is anticipated to become the leading cause of hepatocellular carcinoma (HCC). Accumulating evidence indicates that N6-methyladenosine (m6A)-modified circular RNAs (circRNAs) play key roles in tumor malignant progression. However, the precise molecular mechanisms by which circRNAs and their m6A modification regulatory networks respond to metabolic reprogramming, such as lipid overload stress, to drive malignant tumor progression in the context of MASH-related HCC remain unclear. This study aimed to investigate the role and regulatory network of m6A-modified circRNAs in MASH-related HCC.Methods
Epitranscriptomic microarray and in situ hybridization assays were used to validate
SUBMITTER: Fu J
PROVIDER: S-EPMC12629860 | biostudies-literature | 2025 Nov
REPOSITORIES: biostudies-literature