MIR493
gene geneOn this page
Also known as hsa-mir-493
Summary
MIR493 (microRNA 493, HGNC:32082) is a microRNA gene on chromosome 14q32.2.
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.
Source: NCBI Gene 574450 — RefSeq curated summary.
At a glance
- Gene type: non-coding (miRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:32082 |
| Approved symbol | MIR493 |
| Name | microRNA 493 |
| Location | 14q32.2 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-493 |
| Ensembl gene | ENSG00000207989 |
| Ensembl biotype | miRNA |
| Entrez | 574450 |
| RNAcentral | URS000075C9D6 — miRNA, 89 nt, 25 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000385254
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000385254 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001500260 | 100869060 | 100869148 |
Expression profiles
Bgee: expression breadth broad, 71 present calls, max score 86.22.
Top tissues by expression
71 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| adrenal tissue | UBERON:0018303 | 86.22 | gold quality |
| sural nerve | UBERON:0015488 | 83.91 | gold quality |
| blood | UBERON:0000178 | 83.01 | gold quality |
| monocyte | CL:0000576 | 78.92 | gold quality |
| fundus of stomach | UBERON:0001160 | 78.49 | gold quality |
| muscle of leg | UBERON:0001383 | 78.05 | gold quality |
| calcaneal tendon | UBERON:0003701 | 77.60 | gold quality |
| gastrocnemius | UBERON:0001388 | 77.31 | gold quality |
| right adrenal gland cortex | UBERON:0035827 | 75.09 | gold quality |
| placenta | UBERON:0001987 | 74.45 | gold quality |
| right adrenal gland | UBERON:0001233 | 74.21 | gold quality |
| body of pancreas | UBERON:0001150 | 74.16 | gold quality |
| stomach | UBERON:0000945 | 73.32 | gold quality |
| lung | UBERON:0002048 | 72.78 | gold quality |
| heart left ventricle | UBERON:0002084 | 71.48 | gold quality |
| heart | UBERON:0000948 | 70.82 | gold quality |
| colon | UBERON:0001155 | 70.26 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 70.12 | gold quality |
| endometrium | UBERON:0001295 | 69.85 | gold quality |
| left adrenal gland | UBERON:0001234 | 69.66 | gold quality |
| left ovary | UBERON:0002119 | 69.52 | gold quality |
| omental fat pad | UBERON:0010414 | 68.99 | gold quality |
| right atrium auricular region | UBERON:0006631 | 68.97 | gold quality |
| Ammon’s horn | UBERON:0001954 | 68.69 | gold quality |
| body of stomach | UBERON:0001161 | 68.59 | gold quality |
| ascending aorta | UBERON:0001496 | 68.23 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 67.97 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 67.91 | gold quality |
| thoracic aorta | UBERON:0001515 | 67.89 | gold quality |
| transverse colon | UBERON:0001157 | 67.51 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 1.31 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 40)
- MiRNA-493 was up-regulated in pituitary carcinomas compared to ACTH adenomas (PMID:20960104)
- miR-493 is a new tumor suppressor miRNA in bladder cancer and inhibits cell motility through downregulation of RhoC and FZD4. (PMID:22057916)
- in a subset of colon cancer, upregulation of miR-493 during carcinogenesis prevents liver metastasis via the induction of cell death of metastasized cells. (PMID:22373578)
- MKK7 is a major functional target of miR-493, and its suppression thwarts liver metastasis of colon cancer cells. (PMID:24533778)
- High MIR493 expression is associated with invasion and chemo-resistance in gastric cancer. (PMID:26799283)
- The miR-493-5p/FUT4 pathway has therapeutic potential in breast cancer. (PMID:27375041)
- the existence of a dynamic negative feedback loop in the regulation of IGF1R and miR-493 mediated via Snail, is reported. (PMID:27956702)
- The mechanism of hepatocarcinogenesis and a promising blueprint for miR-493-5p-GP73 axis-oriented treatment of HCC. (PMID:28419971)
- these results demonstrated that miR-493 acts as a tumor suppressor and inhibits cell proliferation and cell cycle in human melanoma by directly targeting IRS4. (PMID:28475006)
- our findings firstly indicate that miR-493-5p levels may play an essential role in NSCLC progression by targeting oncogene ITGB1 suggesting that ITGB1 and miR-493-5p have potential prognostic value as tumor biomarkers in NSCLC patients. (PMID:28537888)
- Novel targets ANTXR1 and RSPO2 were confirmed to be suppressed by miR-493 directly. (PMID:28651234)
- Our results highlight that hyper-methylation of miR-493CpG island might play important roles in the development of lung cancer chemo-resistance by targeting TCRP1, which might be used as a potential therapeutic target in preventing the chemo-resistance of lung cancer. (PMID:28859669)
- MicroRNA 493-5p induced platinum/PARPinhibitor resistance exclusively in BRCA2-mutated carcinomas. (PMID:29617652)
- MiR-493 functioned as tumor suppressor in HCC cells by regulating ZFX expression. Thus, miR-493 may provide potential value for HCC treatment. (PMID:29758928)
- We proved the prognostic role of miR-493 in triple-negative breast cancer (PMID:29777630)
- results suggest that the miR-493-STMN-1 pathway contributes to hypoxia-induced tubular epithelial cell G2/M arrest and renal fibrosis (PMID:30183377)
- acted as a onco-miR in prostate cancer cells and promoted cell proliferation via inhibiting tumor suppresser PHLPP2 expression and activating Akt signaling pathway (PMID:30868840)
- High miR493 expression is associated with osteosarcoma. (PMID:31111286)
- miR-493-5p mediated part of its tumor-suppressor activity by abrogating overexpression of insulin-like growth factor 2 (IGF2) and the IGF2-derived intronic oncomir miR-483-3p in hepatocellular carcinoma cells characterized by IGF2 loss of imprinting. (PMID:31320614)
- Long noncoding RNA GAS6-AS2 sponges microRNA-493, thereby enhancing the malignant characteristics of breast cancer cells via upregulation of FUT4. (PMID:31839366)
- LINC01605 promotes the proliferation of laryngeal squamous cell carcinoma through targeting miR-493-3p. (PMID:31841192)
- MYCN expression levels were inversely correlated with miR-493-5p in tumor tissues. (PMID:31883160)
- MiR-493 Induces Cytotoxic Autophagy in Prostate Cancer Cells through Regulation on PHLPP2. (PMID:32188381)
- MicroRNA-493-5p suppresses colorectal cancer progression via the PI3K-Akt-FoxO3a signaling pathway. (PMID:32373957)
- Molecular Mechanisms and Therapeutic Potential of miR-493 in Cancer. (PMID:32422007)
- Lung cancerassociated transcript 1 facilitates tumorigenesis in laryngeal squamous cell carcinoma through the targeted inhibition of miR493. (PMID:33215214)
- Long non-coding RNA NR2F1-AS1 promoted neuroblastoma progression through miR-493-5p/TRIM2 axis. (PMID:33378023)
- miR-493 by regulating of c-Jun targets Wnt5a/PD-L1-inducing esophageal cancer cell development. (PMID:33793074)
- ILF3-AS1 promotes the aerobic glycolysis and proliferation of melanoma cells by regulating miR-493-5p/PDK1 pathway. (PMID:33913671)
- Circ-CSPP1 knockdown suppresses hepatocellular carcinoma progression through miR-493-5p releasing-mediated HMGB1 downregulation. (PMID:34182091)
- MiR-493-5p inhibits the malignant development of gliomas via suppressing E2F3-mediated dysfunctions of P53 and PI3K/AKT pathways. (PMID:34460057)
- Long coding RNA CCAT2 enhances the proliferation and epithelial-mesenchymal transition of cervical carcinoma cells via the microRNA-493-5p/CREB1 axis. (PMID:34499007)
- Circ_PIP5K1A regulates cisplatin resistance and malignant progression in non-small cell lung cancer cells and xenograft murine model via depending on miR-493-5p/ROCK1 axis. (PMID:34537072)
- Circular RNA circPRKDC promotes tumorigenesis of gastric cancer via modulating insulin receptor substrate 2 (IRS2) and mediating microRNA-493-5p. (PMID:34605348)
- SNHG1 functions as an oncogenic lncRNA and promotes osteosarcoma progression by up-regulating S100A6 via miR-493-5p. (PMID:35130629)
- Overexpression of miR-493-3p suppresses ovarian cancer cell proliferation, migration and invasion through downregulating DPY30. (PMID:35313261)
- Tumor-suppressive MEG3 induces microRNA-493-5p expression to reduce arabinocytosine chemoresistance of acute myeloid leukemia cells by downregulating the METTL3/MYC axis. (PMID:35761379)
- Cancer-associated fibroblasts promote tumor cell growth via miR-493-5p in intrahepatic cholangiocarcinoma. (PMID:36369960)
- LINC00324 promotes cell proliferation and metastasis of esophageal squamous cell carcinoma through sponging miR-493-5p via MAPK signaling pathway. (PMID:36493845)
- Propofol-Induced miR-493-3p Inhibits Growth and Invasion of Gastric Cancer through Suppression of DKK1-Mediated Wnt/beta-Catenin Signaling Activation. (PMID:36762306)
Cross-species orthologs
0 orthologs
Protein
Non-coding RNA — no protein product; not a drug target.
Function
No curated pathway, Gene-Ontology, or interaction data.
Disease & clinical
No curated disease, variant, or cancer-driver associations.
Drugs & pharmacology
No drug or pharmacology data — not an established drug target.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.