circRNA basic information
circBase ID: -
Name: hsa_circ_DOCK1
Synonym: -
Host Gene: DOCK1
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0002108
MONDO name: thyroid cancer
Disease details: thyroid cancer
Disease DO ID:
1781
Disease MeSH ID:
-
Disease NCIt ID:
C7510
Disease ICD11 ID:
447433352
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

thyroid cancer tissues; para-carcinoma tissues; tumor tissues

Cell lines:

FTC-133; TPC-1

In vivo animal model:

-

circRNA-disease information
Expression pattern:
UP
Associated gene: cyclin D1, p53, MMP-9, vimentin, JAK1, STAT3, AMPK
Associated microRNA: miR-124
Biological function: circDOCK1 promotes thyroid cancer cell viability, proliferation, migration and invasion; increases cyclin D1, MMP-9 and vimentin; decreases p53; and activates JAK/STAT/AMPK signaling through downregulation of miR-124.
Molecular mechanism: circDOCK1 downregulates miR-124, thereby inducing phosphorylation of JAK1, STAT3 and AMPK and promoting thyroid cancer cell growth, migration and invasion.
Biological pathway or process:

JAK/STAT (promotes); AMPK (promotes); proliferation (promotes); migration (promotes); invasion (promotes); cell cycle (promotes)

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Transfection; Transwell Assay; Western Blot

Clinical significance:

circDOCK1 was enriched in thyroid carcinoma tissues from 25 patients compared with para-carcinoma tissues.

Description:

circDOCK1 is up-regulated in thyroid carcinoma tissues and acts as a pro-tumor circRNA in human thyroid cancer cell lines. The study suggests that circDOCK1 downregulates miR-124, activates JAK/STAT/AMPK signaling, and thereby promotes cell viability, proliferation, migration and invasion.

Confidence score:

0.5214

Other information
Title:

Circular RNA DOCK1 downregulates microRNA-124 to induce the growth of human thyroid cancer cell lines.

Journal: BioFactors (Oxford, England)
Published: 2020
PubMed ID: 32584497
Study type:

combined biological and clinical study

Data availability: The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Code availability: -