Basic Information
LncRNA/CircRNA Name | LINC-ROR |
Synonyms | LINC-ROR, ROR, lincRNA-RoR |
Region | GRCh38_18:57054558-57072119 |
Ensemble | ENSG00000258609 |
Refseq | NR_048536 |
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 | renal cell carcinoma |
ICD-0-3 | C64.9 |
Methods | qPCR, Western blot, Luciferase reporter assay, etc. |
Sample | RCC tissues, RCC cell lines Caki-1 and Caki-2, and normal human kidney cells HK-2 |
Expression Pattern | up-regulated |
Function Description | ROR was found to be upregulated and microRNA (miR)-206 was found to be downregulated in RCC tissues and cells. Furthermore, the knockdown of ROR inhibited the proliferation, migration and invasion of RCC cells. It was found that ROR binds to miR 206, and that ROR induced cell proliferation and metastasis were reversed by the overexpression of miR 206. In addition, the levels of miR 206 and ROR were negatively correlated in RCC tissues. Furthermore, the overexpression of miR 206 notably suppressed the proliferation, migration and invasion of RCC cells, and these effects were enhanced by the knockdown of vascular endothelial growth factor (VEGF); cell growth and metastasis induced by miR 206 inhibitors could be reversed by the knockdown of VEGF. In addition, the expression levels of miR 206 and VEGF were inversely correlated in RCC samples. In summary, the results of the present study revealed that ROR was upregulated in RCC tissues, which promoted tumor progression by regulating the miR 206/VEGF axis. |
Pubmed ID | 31485634 |
Year | 2019 |
Title | lncRNA ROR promotes the progression of renal cell carcinoma through the miR-206/VEGF axis |
External Links
Links for LINC-ROR | GenBank HGNC NONCODE |
Links for renal cell carcinoma | OMIM COSMIC |