Basic Information
| LncRNA/CircRNA Name | PVT1 |
| Synonyms | NA |
| Region | GRCh38_8:127794533-128101253 |
| Ensemble | ENSG00000249859 |
| Refseq | NR_003367 |
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 | cervical cancer |
| ICD-0-3 | C53 |
| Methods | qPCR, Western blot, Luciferase reporter assay |
| Sample | H8 cell line (the human cervical epithelial immortalized cell line), cervical cancer cell lines, HeLa, Ca Ski and SiHa |
| Expression Pattern | up-regulated |
| Function Description | LncRNA PVT1 overexpression accelerated the growth of cervical cancer cells by advancing the cell cycle and inhibiting cellular apoptosis; increases in Cyclin D1 (CCND1) mRNA and activated Bcl-2 protein expression levels also supported this finding. Furthermore, NF-?B activation and expression was increased by LncRNA PVT1 overexpression. In addition, NF-?B activation or inhibition induced changes in cell viability, accompanied by changes in CCND1 and Bcl-2 expression. Increases or decreases in microRNA-16 (miR-16) expression (using miR mimics and inhibitors) also corresponded to changes in LncRNA PVT1 expression, in vitro. miR-16 mimics and inhibitor had opposite effects to those of NF-?B activity, and miR-16 was demonstrated to directly interact with the NF-?B gene as measured using the dual-luciferase assay. |
| Pubmed ID | 31322217 |
| Year | 2019 |
| Title | Long non-coding RNA plasmacytoma variant translocation 1 gene promotes the development of cervical cancer via the NF-?B pathway |
External Links
| Links for PVT1 | GenBank HGNC NONCODE |
| Links for cervical cancer | OMIM COSMIC |