circRNA basic information
circBase ID: -
Name: hsa_circ_ACAP2
Synonym: circACAP2 / circRNA circACAP2
Host Gene: ACAP2
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
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:

tumor tissues; adjacent normal tissues

Cell lines:

SiHa; HeLa

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: GPX4
Associated microRNA: miR-193a-5p
Biological function: Promotes cervical cancer cell viability/proliferation and suppresses ferroptosis.
Molecular mechanism: circACAP2 acts as a ceRNA (miRNA sponge) for miR-193a-5p to upregulate GPX4, thereby repressing ferroptosis.
Biological pathway or process:

ferroptosis (inhibits); proliferation (promotes); ceRNA regulation (promotes)

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Transfection; CCK8; Luciferase Reporter Assay; RNA Pull-Down Assay; Western Blot

Clinical significance:

circACAP2 expression is upregulated in clinical cervical cancer samples and correlates negatively with miR-193a-5p and positively with GPX4.

Description:

In cervical cancer cells and patient tumor tissues, circACAP2 is upregulated and functions as a ceRNA that sponges miR-193a-5p to increase GPX4 expression. Through the miR-193a-5p/GPX4 axis, circACAP2 promotes cell viability and suppresses ferroptosis-related phenotypes (lipid ROS and iron accumulation).

Confidence score:

0.6672

Other information
Title:

Circular RNA circACAP2 Suppresses Ferroptosis of Cervical Cancer during Malignant Progression by miR-193a-5p/GPX4.

Journal: Journal of oncology
Published: 2022
PubMed ID: 35847361
Study type:

combined biological and clinical study

Data availability: The datasets used during the present study are available from the corresponding author upon request.
Code availability: -