Basic Information
LncRNA/CircRNA Name | KCNQ1OT1 |
Synonyms | NA |
Region | GRCh38_11:2608328-2699994 |
Ensemble | ENSG00000269821 |
Refseq | NR_002728 |
Classification Information
Regulatory Mechanism | Biological Function | Clinical Application | |||
---|---|---|---|---|---|
TF | Immune | Survival | |||
Enhancer | Apoptosis | apoptosis | Drug | Cisplatin | |
Variant | Cell Growth | Circulating | |||
MiRNA | EMT | Metastasis | |||
Methylation | Coding Ability | Recurrence |
Cancer&Entry Information
Cancer Name | tongue squamous cell carcinoma |
ICD-0-3 | C02 |
Methods | Microarray, qPCR, Western blot, Luciferase reporter assay, in vitro knockdown, RIP |
Sample | tongue squamous cell carcinoma tissues, cell lines (CAL27 and SCC9) |
Expression Pattern | up-regulated |
Function Description | Our research showed that the lncRNA KCNQ1OT1 was upregulated in chemo-insensitive TSCC tissues compared with chemo-sensitive TSCC specimens. Meanwhile, high KCNQ1OT1 expression was closely correlated with poor prognosis. Furthermore, KCNQ1OT1 promoted TSCC proliferation and conferred TSCC resistance to cisplatin-induced apoptosis in vitro and in vivo. And miR-211-5p upregulation significantly impaired TSCC proliferation and resumed TSCC chemo-sensitivity, which is contrary to the function of lncRNA KCNQ1OT1. Luciferase experiments confirmed that miR-211-5p harbor binding sites for the 3'-UTRof Ezrin mRNA, and Ezrin/Fak/Src signaling was activated in cisplatin-resistant TSCC cells. Finally, miR-211-5p inhibition in sh-KCNQ1OT1-expressing TSCC cells rescued the suppressed cell proliferation and cisplatin resistance induced by KCNQ1OT1 knockdown. |
Pubmed ID | 29970910 |
Year | 2018 |
Title | LncRNA KCNQ1OT1 Regulates Proliferation and Cisplatin Resistance in Tongue Cancer via miR-211-5p Mediated Ezrin/Fak/Src Signaling |
External Links
Links for KCNQ1OT1 | GenBank HGNC NONCODE |
Links for tongue squamous cell carcinoma | OMIM COSMIC |