Basic Information
LncRNA/CircRNA Name | TUG1 |
Synonyms | NA |
Region | GRCh38_22:30969245-30979395 |
Ensemble | ENSG00000253352 |
Refseq | NR_002323 |
Classification Information
Regulatory Mechanism | Biological Function | Clinical Application | |||
---|---|---|---|---|---|
TF | Immune | Survival | |||
Enhancer | Apoptosis | Drug | |||
Variant | Cell Growth | Circulating | |||
MiRNA | EMT | Metastasis | |||
Methylation | Coding Ability | Recurrence |
Cancer&Entry Information
Cancer Name | colorectal cancer |
ICD-0-3 | C19.9 |
Methods | qPCR, Western blot, Luciferase reporter assay, in vitro knockdown, RIP |
Sample | colorectal cancer tissues, cell lines (HCT116, SW480, HT29, LOVO and SW620) |
Expression Pattern | up-regulated |
Function Description | TUG1 was upregulated in CRC cells, miR-600 was downregulated in CRC tissues, cell lines and CRC metastatic tissues, and low miR-600 expression predicted a poor clinical prognosis. Overexpression of miR-600 suppressed CRC cell migration/invasion and EMT-related proteins in vitro, inhibited tumor volume and weight, and decreased the number of CRC liver metastasis in vivo. KIAA1199 was upregulated in CRC tissues, and was negatively regulated by miR-600. KIAA1199 overexpression promoted CRC cell migration and invasion, which reversed the inhibition effect of miR-600 mimic on migration and invasion of CRC cells. Moreover, TUG1 negatively regulated miR-600, and inhibition of TUG1 suppressed CRC cell migration and invasion and EMT-related proteins via regulating miR-600. Our study proved that TUG1 promoted KIAA1199 expression to accelerate EMT and metastasis of CRC cell through inhibition of miR-600 expression. |
Pubmed ID | 29776371 |
Year | 2018 |
Title | LncRNA TUG1 Promoted KIAA1199 Expression via miR-600 to Accelerate Cell Metastasis and Epithelial-Mesenchymal Transition in Colorectal Cancer |
External Links
Links for TUG1 | GenBank HGNC NONCODE |
Links for colorectal cancer | OMIM COSMIC |