Basic Information
| LncRNA/CircRNA Name | LINC00518 |
| Synonyms | C6orf218 |
| Region | GRCh38_6:10429255-10434874 |
| Ensemble | ENSG00000183674 |
| Refseq | NR_027793 |
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 | breast cancer |
| ICD-0-3 | C50 |
| Methods | qRT-PCR, Western blot assays, Luciferase reporter assays, RIP |
| Sample | Human mammary epithelial cell line (MCF-10A) and human breast cancer cell line (MCF-7), The ADR-resistant variant (MCF-7/ADR) cell line, breast cancer tissue specimens and the adjacent normal tissues |
| Expression Pattern | up-regulated |
| Function Description | linc00518 expression increased nearly 2 fold and MRP1 level elevated about 2.5 fold in breast cancer tissues as compared to that in adjacent normal tissues. miR-199a inhibitor conferred chemoresistance to ADR, VCR and PTX in MCF-7/ADR cells, and suppressing miR-199a reversed multi-drug susceptibility induced by linc00518 knockdown. Furthermore, linc00518 could act as a molecular sponge of miR-199a to repress MRP1 expression. MRP1 depletion increased the sensitivity of MCF-7/ADR cells to ADR, VCR and PTX, and this effect was attenuated following miR-199a inhibition or linc00518 |
| Pubmed ID | 30001527 |
| Year | 2018 |
| Title | Linc00518 Contributes to Multidrug Resistance Through Regulating the MiR-199a/MRP1 Axis in Breast Cancer. |
External Links
| Links for LINC00518 | GenBank HGNC NONCODE |
| Links for breast cancer | OMIM COSMIC |