Apoprotein E methylation is correlated with immune microenvironment in hepatocellular carcinoma.
Apoprotein E
DNA methylation
hepatocellular carcinoma
immune microenvironment
Journal
Acta oncologica (Stockholm, Sweden)
ISSN: 1651-226X
Titre abrégé: Acta Oncol
Pays: England
ID NLM: 8709065
Informations de publication
Date de publication:
Jun 2023
Jun 2023
Historique:
medline:
24
7
2023
pubmed:
23
6
2023
entrez:
23
6
2023
Statut:
ppublish
Résumé
We aimed to evaluate the correlation of apoprotein E (APOE) transcription and its methylation with immune microenvironment in HCC patients. The expression profiles of APOE transcription, APOE methylation, and APOE protein were investigated Based on data from TCGA, GEO, and ICGC datasets, the APOE mRNA was differentially expressed in HCC tissues compared with normal liver tissues. Further, APOE methylation was down-regulated in HCC tissues compared to normal liver tissues. APOE methylation was negatively correlated with APOE transcription in HCC ( APOE methylation had a closer correlation with immune cells than APOE mRNA, indicating that APOE methylation might play an important role in immune regulation in HCC.
Sections du résumé
BACKGROUND
UNASSIGNED
We aimed to evaluate the correlation of apoprotein E (APOE) transcription and its methylation with immune microenvironment in HCC patients.
MATERIAL AND METHODS
UNASSIGNED
The expression profiles of APOE transcription, APOE methylation, and APOE protein were investigated
RESULTS
UNASSIGNED
Based on data from TCGA, GEO, and ICGC datasets, the APOE mRNA was differentially expressed in HCC tissues compared with normal liver tissues. Further, APOE methylation was down-regulated in HCC tissues compared to normal liver tissues. APOE methylation was negatively correlated with APOE transcription in HCC (
CONCLUSION
UNASSIGNED
APOE methylation had a closer correlation with immune cells than APOE mRNA, indicating that APOE methylation might play an important role in immune regulation in HCC.
Identifiants
pubmed: 37352133
doi: 10.1080/0284186X.2023.2225703
doi:
Substances chimiques
Apolipoproteins E
0
Apoproteins
0
RNA, Messenger
0
ApoE protein, human
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM