circRNA basic information
circBase ID: hsa_circ_0007841
Name: hsa_circ_SEC61A1
Synonym: -
Host Gene: sec61a1
Genomic location(hg19): chr3:127778944-127779504:+
Genomic location(hg38): chr3:128060101-128060661:+
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0009693
MONDO name: plasma cell myeloma
Disease details: multiple myeloma
Disease DO ID:
9538
Disease MeSH ID:
D009101
Disease NCIt ID:
C3242
Disease ICD11 ID:
1582389689; 526287100
Disease OMIM ID:
254500
Species: Human
Species details: Homo sapiens
Tissue specimen:

bone marrow

Cell lines:

THP-1; KM3; U266; RPMI-8226; KM3/BTZ; U266/BTZ; RPMI-8226/BTZ

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: -
Associated microRNA: hsa-miR-29b-2-5p, hsa-miR-199a-3p
Biological function: Associated with bortezomib tolerance/drug resistance and poor prognosis in multiple myeloma; suggested as a diagnostic and prognostic biomarker.
Molecular mechanism: Predicted circRNA-miRNA-mRNA interaction network; circRNA acts as a miRNA sponge (e.g., hsa-miR-29b-2-5p; hsa-miR-199a-3p).
Biological pathway or process:

ceRNA regulation (other); drug resistance (promotes)

Detected method:
Q
M
Validation methods:

Microarray; Bioinformatics Analysis; RT-qPCR; Clinical Sample Validation; ROC Analysis; Survival Analysis

Clinical significance:

May be used as a diagnostic marker for MM (AUC 0.907); upregulation correlated with poor prognosis (PFS).

Description:

hsa_circ_0007841 is significantly up-regulated in multiple myeloma bone marrow samples and MM/drug-resistant cell lines. High expression is associated with bortezomib resistance and poorer progression-free survival, and it shows diagnostic potential (ROC AUC ~0.91). Mechanistically, it is proposed to act via a predicted circRNA-miRNA-mRNA network, including sponging hsa-miR-29b-2-5p and hsa-miR-199a-3p.

Confidence score:

0.5534

Other information
Title:

hsa_circ_0007841: A Novel Potential Biomarker and Drug Resistance for Multiple Myeloma.

Journal: Frontiers in oncology
Published: 2019
PubMed ID: 31803627
Study type:

combined biological and clinical study

Data availability: GSE133058
Code availability: -