circRNA basic information
circBase ID: -
Name: hsa_circ_RPPH1
Synonym: circ_RPPH1 / circ-RPPH1
Host Gene: RPPH1
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0004986
MONDO name: urinary bladder carcinoma
Disease details: bladder cancer / BCa
Disease DO ID:
4007
Disease MeSH ID:
-
Disease NCIt ID:
C4912
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

tumor tissues; adjacent normal tissues

Cell lines:

T24; 5637; J82; SV-HUC-1

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: EIF4 A3, N-cadherin mRNA, Vimentin mRNA
Associated microRNA: -
Biological function: promotes proliferation, migration, invasion and EMT in BUC
Molecular mechanism: circ_RPPH1 binds EIF4 A3 and prevents EIF4 A3 recruitment/enrichment on N-cadherin and Vimentin mRNAs, thereby promoting EMT
Biological pathway or process:

proliferation (promotes); migration (promotes); invasion (promotes); EMT (promotes); mRNA stability (other)

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Transfection; Colony Formation Assay; CCK8; Wound Healing Assay; Transwell Assay; RIP (RNA Immunoprecipitation); RNA Pull-Down; Western Blot; Bioinformatics Analysis

Clinical significance:

High circ_RPPH1 levels in BUC correlated with tumor invasion depth.

Description:

circ_RPPH1 is up-regulated in bladder urothelial carcinoma and promotes tumor cell proliferation, migration/invasion and EMT. Mechanistically, circ_RPPH1 binds the RBP EIF4A3 and reduces EIF4A3 enrichment on N-cadherin and Vimentin mRNAs, increasing EMT marker expression and driving EMT.

Confidence score:

0.7045

Other information
Title:

Circ_RPPH1 promotes bladder urothelium carcinoma proliferation and EMT by recruiting and binding to EIF4 A3.

Journal: Hereditas
Published: 2025
PubMed ID: 40346652
Study type:

combined biological and clinical study

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