circRNA basic information
circBase ID: hsa_circ_0000140
Name: hsa_circ_KIAA0907
Synonym: circ_0000140
Host Gene: KIAA0907
Genomic location(hg19): chr1:155891165-155895634:-
Genomic location(hg38): chr1:155921374-155925843:-
Subcellular localization: cytoplasm
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0004958
MONDO name: oral cavity squamous cell carcinoma
Disease details: oral squamous cell carcinoma / OSCC
Disease DO ID:
0050866
Disease MeSH ID:
-
Disease NCIt ID:
C4833
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

tumor tissues

Cell lines:

SCC-15; CAL-27; HOK; SCC-15/DDP; CAL-27/DDP

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: SLC7A11, Ago2
Associated microRNA: miR-527
Biological function: promotes DDP resistance and suppresses ferroptosis in OSCC cells
Molecular mechanism: acts as a molecular sponge for miR-527 to promote SLC7A11 expression, thereby inhibiting ferroptosis and increasing cisplatin resistance
Biological pathway or process:

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

Detected method:
Q
Validation methods:

RT-qPCR; RNase R Treatment; Nuclear-Cytoplasmic Fractionation; Luciferase Reporter Assay; RIP (RNA Immunoprecipitation); RNA Pull-Down; Transfection; MTT; Western Blot; Clinical Sample Validation; Bioinformatics Analysis

Clinical significance:

higher circ_0000140 expression is associated with DDP-resistant OSCC patient tumors

Description:

circ_0000140 is up-regulated in DDP-resistant OSCC tumors and resistant cell lines, where it promotes cisplatin resistance by inhibiting ferroptosis. Mechanistically, it sponges miR-527 to relieve repression of SLC7A11, increasing SLC7A11 and reducing ferroptotic activity, thereby elevating DDP IC50.

Confidence score:

0.788

Other information
Title:

Circ_0000140 Alters miR-527/SLC7A11-Mediated Ferroptosis to Influence Oral Squamous Cell Carcinoma Cell Resistance to DDP.

Journal: Pharmacogenomics and personalized medicine
Published: 2023
PubMed ID: 38105907
Study type:

combined biological and clinical study

Data availability: -
Code availability: -