| HGNC Family | Non-coding RNAs |
| Name | microRNA 6807 |
| Description | microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nRecent studies have shown that miR‑6807‑3p is markedly upregulated in glioma tissues, and this novel microRNA plays an oncogenic role by targeting the tumor suppressor gene DACH1. The dysregulation of miR‑6807‑3p in glioma cells has been linked to enhanced tumor progression, underscoring its importance in regulating key cellular processes in the disease."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFunctional investigations using RT‑qPCR, western blot, and luciferase reporter assays have demonstrated that miR‑6807‑3p directly binds to the 3′‑UTR of DACH1, thereby modulating its expression. As a result, increased miR‑6807‑3p levels promote cell proliferation, enhance migratory potential, inhibit apoptosis, and lessen cell cycle arrest in glioma cells."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nImportantly, the tumor‑promoting effects of miR‑6807‑3p are mitigated upon overexpression of DACH1, suggesting that the miR‑6807‑3p/DACH1 axis plays a critical role in glioma advancement and might represent a promising target for therapeutic intervention. The correlation between aberrant miR‑6807‑3p expression and clinical outcomes further highlights its potential clinical relevance in managing glioma."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Gui-Feng Lu, Fei Geng, Zhi Xiao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MicroRNA-6807-3p promotes the tumorigenesis of glioma by targeting downstream DACH1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Brain Res (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.brainres.2018.12.008"}], "href": "https://doi.org/10.1016/j.brainres.2018.12.008"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30527681"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30527681"}]}]}]}
|
| Synonyms | HSA-MIR-6807 |
| NCBI Gene ID | 102465976 |
| API | |
| Download Associations | |
| Predicted Functions |
![]() |
| Co-expressed Genes |
![]() |
| Expression in Tissues and Cell Lines |
![]() |
MIR6807 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
Click the + buttons to view associations for MIR6807 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary |
|---|