circRNA basic information
circBase ID: -
Name: -
Synonym: circRNA‐SORE / circRNA_104797
Host Gene: -
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: cytoplasm
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0007256
MONDO name: hepatocellular carcinoma
Disease details: hepatocellular carcinoma / HCC
Disease DO ID:
684, 686
Disease MeSH ID:
D006528
Disease NCIt ID:
C3099
Disease ICD11 ID:
1294035808
Disease OMIM ID:
114550
Species: Human
Species details: Homo sapiens
Tissue specimen:

HCC tumor specimens; xenografts

Cell lines:

HepG2; HCC‐LM3; SK‐Hep‐1

In vivo animal model:

patient-derived xenograft

circRNA-disease information
Expression pattern:
UP
Associated gene: UBQLN1, GPX4, YBX1
Associated microRNA: -
Biological function: Promotes sorafenib resistance by regulating intracellular ROS levels and inhibiting ferroptosis; maintains mitochondrial integrity and redox homeostasis.
Molecular mechanism: Binds and stabilizes UBQLN1 to prevent its proteasomal degradation; UBQLN1 stabilizes GPX4 (STI-domain dependent), inhibiting GPX4 proteasomal degradation and suppressing ferroptosis under sorafenib-induced oxidative stress.
Biological pathway or process:

ferroptosis (inhibits); mitochondrial function (promotes); oxidative phosphorylation (other); drug resistance (promotes)

Detected method:
Q
Validation methods:

RT-qPCR; Transfection; Western Blot; Flow Cytometry(Non-apoptosis/cycle); In Vivo Animal Model; Bioinformatics Analysis; RNA Pull-Down; RIP (RNA Immunoprecipitation); Co-IP; IF (Immunofluorescence)

Clinical significance:

-

Description:

circRNA-SORE is up-regulated in sorafenib-resistant HCC cells and promotes drug resistance by reducing ROS and suppressing ferroptosis. It directly binds and stabilizes UBQLN1, which in turn stabilizes GPX4 and preserves redox/mitochondrial homeostasis under sorafenib-induced stress.

Confidence score:

0.6562

Other information
Title:

circRNA-SORE/UBQLN1/GPX4 Mediates the Acquisition of Sorafenib Resistance in Hepatocellular Carcinoma Through Inhibition of Ferroptosis.

Journal: MedComm
Published: 2025
PubMed ID: 41287824
Study type:

combined biological and clinical study

Data availability: Datasets used and/or analyzed are available upon reasonable request to the corresponding author.
Code availability: -