circRNA basic information
circBase ID: -
Name: hsa_circ_CRKL
Synonym: circCRKL
Host Gene: CRKL
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: cytoplasm
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0008315
MONDO name: prostate cancer
Disease details: prostate cancer
Disease DO ID:
10283
Disease MeSH ID:
D011471
Disease NCIt ID:
C7378
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

PCa tissues; adjacent normal tissues; tumor tissues

Cell lines:

RWPE-1; C4-2; DU145; LNCaP; 22Rv1

In vivo animal model:

cell line-derived xenograft

circRNA-disease information
Expression pattern:
DN
Associated gene: KLF5
Associated microRNA: miR-141
Biological function: circCRKL acts as a tumor suppressor in PCa; overexpression represses cell cycle progression, migration, invasion, tumor growth, and promotes apoptosis.
Molecular mechanism: circCRKL sponges miR-141 to positively regulate KLF5 expression, thereby suppressing PCa progression.
Biological pathway or process:

ceRNA regulation (other); cell cycle (inhibits); migration (inhibits); invasion (inhibits); apoptosis (promotes); proliferation (inhibits)

Detected method:
Q
Validation methods:

RNase R Treatment; RT-qPCR; Nuclear-Cytoplasmic Fractionation; Clinical Sample Validation; Bioinformatics Analysis; Luciferase Reporter Assay; RIP (RNA Immunoprecipitation); RNA Pull-Down; Transfection; Cell Cycle Assay; Annexin V/PI Flow Cytometry; Wound Healing Assay; Transwell Assay; Western Blot; In Vivo Animal Model

Clinical significance:

circCRKL might be an underlying therapeutic target for PCa treatment.

Description:

circCRKL is down-regulated in prostate cancer tissues and cell lines and functions as a tumor suppressor. Mechanistically, circCRKL sponges miR-141 to upregulate KLF5, thereby inhibiting cell cycle progression, migration, invasion, and in vivo tumor growth while promoting apoptosis.

Confidence score:

0.7981

Other information
Title:

circCRKL suppresses the progression of prostate cancer cells by regulating the miR-141/KLF5 axis.

Journal: Pathology, research and practice
Published: 2020
PubMed ID: 32919302
Study type:

combined biological and clinical study

Data availability: TCGA; Supplementary material related to this article can be found, in the online version, at doi:https://doi.org/10.1016/j.prp.2020.153182
Code availability: -