circRNA basic information
circBase ID: mmu_circ_0004175
Name: mmu_circ_Hif1a
Synonym: circHif1a
Host Gene: Hif1a
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0007254
MONDO name: breast cancer
Disease details: breast cancer
Disease DO ID:
1612
Disease MeSH ID:
-
Disease NCIt ID:
C9335
Disease ICD11 ID:
1047754165
Disease OMIM ID:
-
Species: Mouse
Species details: Mus musculus
Tissue specimen:

-

Cell lines:

4T1

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: P-gp, Abcb1b, ADAR2
Associated microRNA: miR-195a-3p
Biological function: circHif1a functions as a sponge for miR-195a-3p, upregulates P-gp/Abcb1b expression, reduces intracellular doxorubicin accumulation, and contributes to decreased susceptibility to doxorubicin in murine breast cancer cells.
Molecular mechanism: ADAR2 suppresses circHif1a biogenesis; increased circHif1a sponges miR-195a-3p, relieving miR-195a-3p-mediated repression of Abcb1b/P-gp and promoting chemoresistance.
Biological pathway or process:

ceRNA regulation (promotes); drug resistance (promotes); chemoresistance (promotes); other pathway/process (promotes)

Detected method:
Q
Validation methods:

Back-Splice Junction PCR / divergent primers PCR; RNase R Treatment; Sanger Sequencing; RT-qPCR; Luciferase Reporter Assay; Transfection; Western Blot; Bioinformatics Analysis

Clinical significance:

May help improve drug efficacy by clarifying the mechanism of chemoresistance in breast cancer.

Description:

In murine 4T1 breast cancer cells, ADAR2 knockdown increases circHif1a expression. circHif1a acts as a miR-195a-3p sponge, causing increased Abcb1b/P-gp expression and reduced susceptibility to doxorubicin, thereby contributing to chemoresistance.

Confidence score:

0.686

Other information
Title:

RNA editing enzyme ADAR2 regulates P-glycoprotein expression in murine breast cancer cells through the circRNA-miRNA pathway.

Journal: Biochemical and biophysical research communications
Published: 2024
PubMed ID: 38917633
Study type:

biological research

Data availability: GSE245962; GSE132568; Supplementary data; https://doi.org/10.1016/j.bbrc.2024.150289
Code availability: -