Basic Information
LncRNA/CircRNA Name | FTX |
Synonyms | NA |
Region | GRCh38_X:73946555-74293574 |
Ensemble | ENSG00000230590 |
Refseq | NR_028379 |
Classification Information
Regulatory Mechanism | Biological Function | Clinical Application | |||
---|---|---|---|---|---|
TF | Immune | Survival | |||
Enhancer | Apoptosis | 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, Luciferase reporter assay etc. |
Sample | CRC tissues, cell lines (FHC, HT-29, HCT-8, COLO 205, SW480 and LoVo) |
Expression Pattern | up-regulated |
Function Description | FTX was up-regulated in CRC tissues and cell lines, knockdown of FTX inhibited CRC cell proliferation, migration and invasion in vitro as well as suppressed CRC tumor growth in vivo. FTX was confirmed to directly bind to miR-192-5p and negatively regulated miR-192-5p expression in CRC cells. |
Pubmed ID | 32280242 |
Year | 2020 |
Title | FTX was up-regulated in CRC tissues and cell lines, knockdown of FTX inhibited CRC cell proliferation, migration and invasion in vitro as well as suppressed CRC tumor growth in vivo. FTX was confirmed to directly bind to miR-192-5p and negatively regulated miR-192-5p expression in CRC cells. Besides that overexpressed FTX positively modulated EIF5A2, a direct target of miR-192-5p, via miR-192-5p in CRC cells. Importantly, the inhibitory activities on CRC progression mediated by FTX deletion were reversed miR-192-5p down-regulation or EIF5A2 up-regulation. |
External Links
Links for FTX | GenBank HGNC NONCODE |
Links for colorectal cancer | OMIM COSMIC |