circRNA basic information
circBase ID: hsa_circ_0001017
Name: hsa_circ_XPO1
Synonym: circXPO1
Host Gene: XPO1
Genomic location(hg19): chr2:61749745-61761038:-
Genomic location(hg38): chr2:61522610-61533903:-
Subcellular localization: cytoplasm
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005575
MONDO name: colorectal cancer
Disease details: colorectal cancer / CRC
Disease DO ID:
5672, 9256
Disease MeSH ID:
-
Disease NCIt ID:
C4978
Disease ICD11 ID:
-
Disease OMIM ID:
114500
Species: Human
Species details: Homo sapiens
Tissue specimen:

CRC tissues; adjacent normal tissues; tumors; liver

Cell lines:

FHC; LoVo; SW480; SW620; HCT116; HCT-8

In vivo animal model:

cell line-derived xenograft

circRNA-disease information
Expression pattern:
UP
Associated gene: ALKBH5, IGF2BP1, IGF2BP2, IGF2BP3, FMRP, WWC2
Associated microRNA: -
Biological function: promotes CRC cell growth, metastasis, and EMT in vitro and in vivo
Molecular mechanism: ALKBH5 down-regulation enhances IGF2BP2-mediated m6A modification to increase circXPO1; circXPO1 binds FMRP and promotes WWC2 mRNA decay, activating Hippo-YAP signaling
Biological pathway or process:

Hippo/YAP (promotes); EMT (promotes); proliferation (promotes); migration (promotes); invasion (promotes); metastasis (promotes); m6A modification (promotes); mRNA stability (inhibits)

Detected method:
Q
Validation methods:

Back-Splice Junction PCR / divergent primers PCR; RNase R Treatment; Sanger Sequencing; Actinomycin D / DRB Stability Assay; RT-qPCR; FISH / smFISH; Nuclear-Cytoplasmic Fractionation; Clinical Sample Validation; Transfection; Colony Formation Assay; Wound Healing Assay; Transwell Assay; MeRIP / MeRIP-seq; RIP (RNA Immunoprecipitation); RNA Pull-Down; Western Blot; IHC (Immunohistochemistry); In Vivo Animal Model; H&E Staining; Survival Analysis; Bioinformatics Analysis

Clinical significance:

high expression of circXPO1 indicated a lower survival rate of CRC patients

Description:

circXPO1 (hsa_circ_0001017), derived from XPO1, is up-regulated in colorectal cancer and predicts poor survival. It is mainly cytoplasmic and promotes CRC growth, EMT, invasion and metastasis by an m6A-dependent mechanism (ALKBH5/IGF2BP2) and by binding the RBP FMRP to destabilize WWC2 mRNA, thereby activating Hippo-YAP signaling.

Confidence score:

0.8912

Other information
Title:

m6A-modified circXPO1 accelerates colorectal cancer progression via interaction with FMRP to promote WWC2 mRNA decay.

Journal: Journal of translational medicine
Published: 2024
PubMed ID: 39402642
Study type:

combined biological and clinical study

Data availability: All data generated or analyzed during this study are included in this published article.
Code availability: -