circRNA basic information
circBase ID: -
Name: hsa_circ_FOXP1
Synonym: circFOXP1
Host Gene: FOXP1
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005047
MONDO name: infertility disorder
Disease details: recurrent pregnancy loss
Disease DO ID:
5223
Disease MeSH ID:
D007246
Disease NCIt ID:
C3836
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

placental tissues

Cell lines:

HTR8/SVneo

In vivo animal model:

-

circRNA-disease information
Expression pattern:
DN
Associated gene: S100A11
Associated microRNA: miR-143-3p
Biological function: enhances proliferation/viability, restrains apoptosis, and facilitates EMT-associated migration and invasion of trophoblastic cells (relieves trophoblastic cell dysfunction in RPL).
Molecular mechanism: circFOXP1 acts as a ceRNA that competitively binds miR-143-3p to upregulate S100A11 in trophoblastic cells.
Biological pathway or process:

proliferation (promotes); apoptosis (inhibits); migration (promotes); invasion (promotes); EMT (promotes); ceRNA regulation (other)

Detected method:
Q
Validation methods:

RT-qPCR; Western Blot; Luciferase Reporter Assay; Transfection; CCK8; Annexin V/PI Flow Cytometry; Wound Healing Assay; Transwell Assay; Bioinformatics Analysis; Clinical Sample Validation

Clinical significance:

potential biomarkers and diagnostic targets for RPL

Description:

circFOXP1 is down-regulated in RPL placental tissues. It alleviates trophoblastic cell dysfunction by acting as a miR-143-3p sponge to upregulate S100A11, thereby promoting proliferation/viability, EMT, migration and invasion, and inhibiting apoptosis.

Confidence score:

0.6536

Other information
Title:

Circular RNA FOXP1 relieves trophoblastic cell dysfunction in recurrent pregnancy loss via the miR-143-3p/S100A11 cascade.

Journal: Bioengineered
Published: 2021
PubMed ID: 34654357
Study type:

combined biological and clinical study

Data availability: The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Code availability: -