circRNA basic information
circBase ID: -
Name: hsa_circ_SEPT9
Synonym: circular RNA septin 9
Host Gene: SEPT9
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005494
MONDO name: triple-negative breast carcinoma
Disease details: triple negative breast cancer
Disease DO ID:
0060081
Disease MeSH ID:
D064726
Disease NCIt ID:
C71732
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

-

Cell lines:

MDA-MB-157; MDA-MB-468; HCC1806; MCF10A; MDA-MB-468/DDP

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: SRSF1, GCH1
Associated microRNA: -
Biological function: circSEPT9 reduces DDP chemosensitivity of TNBC cells, inhibits ferroptosis, increases colony formation, and stabilizes GCH1 protein by blocking GCH1 ubiquitination.
Molecular mechanism: SRSF1 binds to and upregulates circSEPT9; circSEPT9 binds GCH1 and blocks GCH1 ubiquitination, increasing GCH1 protein stability, thereby inhibiting ferroptosis and reducing cisplatin chemosensitivity.
Biological pathway or process:

ferroptosis (inhibits); chemoresistance (promotes); proliferation (promotes); ubiquitination (inhibits); drug resistance (promotes)

Detected method:
Q
Validation methods:

RT-qPCR; RNase R Treatment; Actinomycin D / DRB Stability Assay; RIP (RNA Immunoprecipitation); RNA Pull-Down; Transfection; CCK8; Colony Formation Assay; Western Blot; Bioinformatics Analysis

Clinical significance:

-

Description:

In TNBC cells, circSEPT9 is upregulated, especially in DDP-resistant cells. SRSF1 binds and promotes circSEPT9, while circSEPT9 binds GCH1 and blocks its ubiquitination, stabilizing GCH1 protein. This circSEPT9/GCH1 mechanism inhibits ferroptosis and reduces cisplatin chemosensitivity.

Confidence score:

0.7363

Other information
Title:

SRSF1 inhibits ferroptosis and reduces cisplatin chemosensitivity of triple-negative breast cancer cells through the circSEPT9/GCH1 axis.

Journal: Journal of proteomics
Published: 2024
PubMed ID: 38040194
Study type:

biological research

Data availability: No
Code availability: -