Basic Information
| LncRNA/CircRNA Name | MEF2C-AS1 |
| Synonyms | NA |
| Region | GRCh38_5:88883328-89466398 |
| Ensemble | ENSG00000248309 |
| Refseq | NR_104031 |
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 | gastric cancer |
| ICD-0-3 | C16 |
| Methods | RNA-seq, qPCR, Western blot, in vitro knockdown |
| Sample | gastric cancer tissues, cell lines (AGS and SNU-1), gastric cancer plasma |
| Expression Pattern | down-regulated |
| Function Description | Validation data showed MEF2C-AS1 and FENDRR were significantly downregulated in tumor tissues compared with normal tissues. And decreased FENDRR are associated with aggressive tumor characteristics including more advanced stage (P = .030), poor differentiation (P = .043) and lymphatic metastasis (P = .001). The expression level MEF2C-AS1 was significantly lower in DGC patients' plasma than that in healthy controls' plasma. In gastric cancer cell lines, knock-down of MEF2C-AS1 or FENDRR reduced the protein levels of FAT3, NTN1 and LYVE1 (the co-expressed genes), which were related with gastric cancer cell proliferation and invasion by previous studies. In addition, knock-down of MEF2C-AS1 or FENDRR promoted aggressive tumor behaviors in in-vitro assays. |
| Pubmed ID | 30005210 |
| Year | 2018 |
| Title | Characterization of Long Non-Coding RNAs and MEF2C-AS1 Identified as a Novel Biomarker in Diffuse Gastric Cancer |
External Links
| Links for MEF2C-AS1 | GenBank HGNC NONCODE |
| Links for gastric cancer | OMIM COSMIC |