MIR655
gene geneOn this page
Also known as hsa-mir-655
Summary
MIR655 (microRNA 655, HGNC:32911) is a microRNA gene on chromosome 14q32.31.
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 724025 — 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:32911 |
| Approved symbol | MIR655 |
| Name | microRNA 655 |
| Location | 14q32.31 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-655 |
| Ensembl gene | ENSG00000207646 |
| Ensembl biotype | miRNA |
| Entrez | 724025 |
| RNAcentral | URS000075B3AB — miRNA, 97 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000362159
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000362159 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001436922 | 101049550 | 101049646 |
Expression profiles
Bgee: expression breadth broad, 53 present calls, max score 93.21.
Top tissues by expression
53 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| adrenal tissue | UBERON:0018303 | 93.21 | gold quality |
| lung | UBERON:0002048 | 84.29 | gold quality |
| stomach | UBERON:0000945 | 80.05 | gold quality |
| placenta | UBERON:0001987 | 79.69 | gold quality |
| body of pancreas | UBERON:0001150 | 77.20 | gold quality |
| heart | UBERON:0000948 | 73.27 | gold quality |
| adenohypophysis | UBERON:0002196 | 73.26 | gold quality |
| gastrocnemius | UBERON:0001388 | 72.89 | gold quality |
| right atrium auricular region | UBERON:0006631 | 72.14 | gold quality |
| kidney | UBERON:0002113 | 72.03 | gold quality |
| intestine | UBERON:0000160 | 71.51 | gold quality |
| left ovary | UBERON:0002119 | 71.47 | gold quality |
| colon | UBERON:0001155 | 70.69 | gold quality |
| right coronary artery | UBERON:0001625 | 69.51 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 69.41 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 68.92 | gold quality |
| omental fat pad | UBERON:0010414 | 68.88 | gold quality |
| left adrenal gland | UBERON:0001234 | 68.78 | gold quality |
| esophagus mucosa | UBERON:0002469 | 68.27 | gold quality |
| descending thoracic aorta | UBERON:0002345 | 68.08 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 67.83 | gold quality |
| Ammon’s horn | UBERON:0001954 | 67.73 | gold quality |
| ascending aorta | UBERON:0001496 | 67.50 | gold quality |
| muscle layer of sigmoid colon | UBERON:0035805 | 67.49 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 67.33 | gold quality |
| thoracic mammary gland | UBERON:0005200 | 67.17 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 67.00 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 66.95 | gold quality |
| transverse colon | UBERON:0001157 | 66.62 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 66.32 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.14 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 21)
- ZEB1 and TGFBR2 identified as direct targets of miR-655 (PMID:23690952)
- Data show that the miR-134/487b/655 cluster regulates TGF-beta1-induced epithelial-mesenchymal transition and affected the resistance to gefitinib by directly targeting membrane-associated guanylate kinase, WW, and PDZ domain-containing protein 2 (MAGI2). (PMID:24258346)
- Report feedback loop between PTTG1 targeting miRNAs,including mir655, PTTG1 and p53 that promotes pituitary tumorigenesis. (PMID:26320179)
- Results showed that MiR-655-3p was significantly decreased in hepatocellular carcinoma (HCC) clinical specimens and cell lines. Overexpression of miR-655-3p suppressed cell proliferation, migration and invasion of HCC in vitro. The study suggests that MiR-655-3p might functions as a tumor suppressor by directly targeting ADAM10 and indirectly regulating beta-catenin pathway in the development of progression of HCC. (PMID:27259866)
- MiR-655-3p showed a 6.79-fold decrease in expression after 12 h exposure compared to 0 h, was predicted in silico to bind ABCG2 3’-UTR and showed a significant negative correlation (p = 0.01) to ABCG2 expression level. (PMID:28990842)
- miR655 is an oncogenic miRNA in human breast cancer, promoting EMT, cellular migration, invasion, proliferation, SLC stimulation and metastasis in vivo. (PMID:29321644)
- Low levels of miR-655 in plasma relate to lymphatic progression. (PMID:30609933)
- MiR-655-3p inhibited proliferation and migration of ovarian cancer cells by targeting RAB1A. (PMID:31114987)
- MicroRNA-655-3p and microRNA-497-5p inhibit cell proliferation in cultured human lip cells through the regulation of genes related to human cleft lip (PMID:31122291)
- This study establishes the dynamic functions of miR526b/miR655 in oxidative stress induction in breast cancer. (PMID:31430859)
- SP1-induced lncRNA LINC00689 overexpression contributes to osteosarcoma progression via the miR-655/SOX18 axis. (PMID:32196572)
- MiR-655-3p inhibits the progression of osteoporosis by targeting LSD1 and activating BMP-2/Smad signaling pathway. (PMID:32431171)
- TUG1 weakens the sensitivity of acute myeloid leukemia cells to cytarabine by regulating miR-655-3p/CCND1 axis. (PMID:32432757)
- Long noncoding RNA LINC01194 enhances the malignancy of laryngeal squamous cell carcinoma by sponging miR-655 to increase SOX18 expression. (PMID:32703403)
- MiR-655-3p inhibits growth and invasiveness of trophoblasts via targeting PBX3 and thus deteriorates preeclampsia. (PMID:33155190)
- Alteration of Pituitary Tumor Transforming Gene 1 by MicroRNA-186 and 655 Regulates Invasion Ability of Human Oral Squamous Cell Carcinoma. (PMID:33498448)
- Circular RNA circ_0001955 promotes hepatocellular carcinoma tumorigenesis by up-regulating alkaline ceramidase 3 expression through microRNA-655-3p. (PMID:35034572)
- Long noncoding RNA endogenous bornavirus-like nucleoprotein acts as an oncogene by regulating microRNA-655-3p expression in T-cell acute lymphoblastic leukemia. (PMID:35220878)
- CCN2 Facilitates IL-17 Production and Osteoclastogenesis in Human Osteoarthritis Synovial Fibroblasts by Inhibiting miR-655 Expression. (PMID:35876037)
- Exosomal miR-655-3p inhibits growth, and invasion and macrophage M2 polarization through targeting CXCR4 in papillary thyroid carcinoma. (PMID:36512648)
- Circ-LDLRAD3/miR-655-3p/MAPK1 axis enhances cell migration and invasion in papillary thyroid carcinoma. (PMID:38430029)
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.