circRNA basic information
circBase ID: -
Name: hsa_circ_DUSP22
Synonym: circDUSP22
Host Gene: DUSP22
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: cytoplasm
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0008315
MONDO name: prostate cancer
Disease details: prostate cancer / PCa
Disease DO ID:
10283
Disease MeSH ID:
D011471
Disease NCIt ID:
C7378
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

plasma; tissue

Cell lines:

DU145; PC3; PC-3; RWPE-1

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: SLC7A11, GPX4, DDX39A
Associated microRNA: miR-18a-5p
Biological function: promotes proliferation, migration and invasion; inhibits ferroptosis in prostate cancer cells
Molecular mechanism: circDUSP22 acts as a ceRNA sponge for miR-18a-5p to upregulate SLC7A11 and GPX4, thereby attenuating ferroptosis
Biological pathway or process:

ferroptosis (inhibits); ceRNA regulation (other)

Detected method:
Q
M
Validation methods:

Microarray; RT-qPCR; RNase R Treatment; Actinomycin D / DRB Stability Assay; FISH / smFISH; Nuclear-Cytoplasmic Fractionation; Clinical Sample Validation; Luciferase Reporter Assay; RNA Pull-Down; Transfection; CCK8; Colony Formation Assay; Transwell Assay; Wound Healing Assay; Western Blot; IHC (Immunohistochemistry); Bioinformatics Analysis

Clinical significance:

The elevated expression of circDUSP22 in plasma may serve as a potential biomarker for diagnosing prostate cancer.

Description:

circDUSP22 is up-regulated in prostate cancer plasma and cell lines and promotes malignant phenotypes (proliferation, migration, invasion). Mechanistically, it sponges miR-18a-5p to increase SLC7A11 (and GPX4), thereby inhibiting ferroptosis.

Confidence score:

0.8537

Other information
Title:

CircDUSP22 Attenuates the Ferroptosis of Prostate Cancer Cells via miR-18a-5p/SLC7A11/GPX4 Signaling.

Journal: Combinatorial chemistry & high throughput screening
Published: 2025
PubMed ID: 38994627
Study type:

combined biological and clinical study

Data availability: The data and supportive information are available within the article.
Code availability: -