circRNA basic information
circBase ID: -
Name: hsa_circ_FBXW7
Synonym: circFBXW7
Host Gene: FBXW7
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0018874
MONDO name: acute myeloid leukemia
Disease details: acute myeloid leukemia / AML
Disease DO ID:
9119
Disease MeSH ID:
D015470
Disease NCIt ID:
C3171
Disease ICD11 ID:
-
Disease OMIM ID:
601626
Species: Human
Species details: Homo sapiens
Tissue specimen:

bone marrow; blood; AML patient blasts

Cell lines:

KG-1a; OCI-AML3

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UN
Associated gene: -
Associated microRNA: -
Biological function: circFBXW7 acts as a tumor suppressor in AML and regulates the proliferative capacity of AML blasts; circFBXW7 knockdown increased proliferation and colony formation.
Molecular mechanism: The mechanism is unlikely to be miRNA sequestration; high circFBXW7 expression was associated with genes involved in chromatin state, transcription, leukocyte activation and differentiation, whereas low expression was associated with stem cell properties and WNT/beta-catenin and NOTCH signaling.
Biological pathway or process:

proliferation (inhibits); Wnt/beta-catenin (inhibits); Notch (inhibits); stemness (inhibits); other pathway/process (promotes)

Detected method:
Q
S
Validation methods:

RNA-seq; RT-qPCR; RNase R Treatment; Back-Splice Junction PCR / divergent primers PCR; Sanger Sequencing; Transfection; BrdU; Colony Formation Assay; Bioinformatics Analysis

Clinical significance:

-

Description:

circFBXW7 functions as a tumor suppressor-like circRNA in AML. Its knockdown increases proliferation of AML cell lines and colony formation by patient AML blasts, and its mechanism is unlikely to involve miRNA sequestration based on lack of detectable miRNA-binding sites.

Confidence score:

0.6716

Other information
Title:

Clinical and functional significance of circular RNAs in cytogenetically normal AML.

Journal: Blood advances
Published: 2020
PubMed ID: 31945158
Study type:

combined biological and clinical study

Data availability: -
Code availability: -