circRNA basic information
circBase ID: -
Name: hsa_circ_PRDM4
Synonym: circPRDM4
Host Gene: PRDM4
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: cytoplasm
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0002974
MONDO name: cervical cancer
Disease details: cervical cancer / CC
Disease DO ID:
4362
Disease MeSH ID:
-
Disease NCIt ID:
C9311
Disease ICD11 ID:
1256072522
Disease OMIM ID:
603956
Species: Human
Species details: Homo sapiens
Tissue specimen:

-

Cell lines:

HeLa; SiHa; HeLa/DDP; SiHa/DDP

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: USF1
Associated microRNA: -
Biological function: promotes chemoresistance to cisplatin, promotes immune escape, and promotes tumorigenesis (proliferation, migration, invasion) in cervical cancer cells
Molecular mechanism: USF1 transcriptionally induces circPRDM4 expression; the USF1/circPRDM4 axis regulates immune escape and tumorigenesis in chemoresistant cervical cancer cells
Biological pathway or process:

proliferation (promotes); migration (promotes); invasion (promotes); immune regulation (other); drug resistance (promotes)

Detected method:
Q
M
Validation methods:

Microarray; RT-qPCR; RNase R Treatment; Actinomycin D / DRB Stability Assay; Nuclear-Cytoplasmic Fractionation; Transfection; CCK8; Colony Formation Assay; Transwell Assay; ELISA; IF (Immunofluorescence); ChIP / ChIP-seq; Luciferase Reporter Assay; Western Blot; Bioinformatics Analysis

Clinical significance:

-

Description:

circPRDM4 is up-regulated in cisplatin-chemoresistant cervical cancer cells and promotes chemoresistance, immune escape, and malignant phenotypes (proliferation, migration, invasion). USF1 transcriptionally induces circPRDM4, forming a USF1/circPRDM4 axis that drives these behaviors.

Confidence score:

0.7735

Other information
Title:

USF1 regulated circPRDM4 modulates tumorigenesis and immune escape in chemoresistant cervical cancer.

Journal: Journal of cellular and molecular medicine
Published: 2024
PubMed ID: 37665075
Study type:

biological research

Data availability: The data supporting this study's findings are available from the corresponding author upon reasonable request.
Code availability: -