MIR154

gene
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Also known as hsa-mir-154

Summary

MIR154 (microRNA 154, HGNC:31541) 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 406946 — 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

FieldValue
HGNC IDHGNC:31541
Approved symbolMIR154
NamemicroRNA 154
Location14q32.31
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-154
Ensembl geneENSG00000207978
Ensembl biotypemiRNA
Entrez406946
RNAcentralURS00003AF18B — miRNA, 84 nt, 7 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000385243

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000385243 — 1 exons

ExonStartEnd
ENSE00001500249101059755101059838

Expression profiles

Bgee: expression breadth broad, 65 present calls, max score 95.95.

Top tissues by expression

65 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
adrenal tissueUBERON:001830395.95gold quality
placentaUBERON:000198781.81gold quality
stomachUBERON:000094580.14gold quality
bloodUBERON:000017878.71gold quality
gastrocnemiusUBERON:000138877.21gold quality
left ovaryUBERON:000211975.77gold quality
intestineUBERON:000016075.04gold quality
ovaryUBERON:000099274.96gold quality
heartUBERON:000094874.95gold quality
kidneyUBERON:000211374.70gold quality
lungUBERON:000204874.55gold quality
liverUBERON:000210772.23gold quality
tibial arteryUBERON:000761071.40gold quality
heart left ventricleUBERON:000208471.33gold quality
right atrium auricular regionUBERON:000663170.81gold quality
colonUBERON:000115570.47gold quality
body of stomachUBERON:000116169.88gold quality
endometriumUBERON:000129569.45gold quality
adipose tissueUBERON:000101369.37gold quality
skin of abdomenUBERON:000141669.33gold quality
omental fat padUBERON:001041469.31gold quality
myometriumUBERON:000129669.21gold quality
small intestine Peyer’s patchUBERON:000345468.76gold quality
corpus callosumUBERON:000233668.75gold quality
prefrontal cortexUBERON:000045167.99gold quality
esophagogastric junction muscularis propriaUBERON:003584167.58gold quality
upper lobe of left lungUBERON:000895267.52gold quality
right hemisphere of cerebellumUBERON:001489066.70gold quality
minor salivary glandUBERON:000183066.62gold quality
left adrenal glandUBERON:000123466.60gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.37

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 38)

  • Expression of miR-154*, miR-376b, and miR-431* were suppressed in leukocytes from initial Grave disease patients. (PMID:22456620)
  • Increases in mir-154 may allow the activation of fibrotic transcriptional programs in lung fibroblasts. (PMID:23043088)
  • miR-154 plays a prominent role in prostate cancer proliferation by suppressing CCND2 (PMID:23428540)
  • MiR-154 plays a role in regulating epithelial-mesenchymal transition by targeting HMGA2. (PMID:23591597)
  • Mir-154, mapped to the 14q32.31 locus, regulates proliferation, apoptosis, migration and invasion in metastatic prostate cancer cells. (PMID:24166498)
  • The toll-like receptor 2 is a direct target of miR-154 in colorectal cancer cells. (PMID:24242044)
  • miR-154* and miR-379 play important roles in prostate cancer biology by facilitating tumor growth, EMT, and bone metastasis. (PMID:25324143)
  • our results indicate that changes in serum miRNAs are associated with cigarette smoking and lung cancer and that let-7i-3p and miR-154-5p are potential biomarkers of smoking-related lung cancer. (PMID:25386559)
  • miR-154-5p may play an important role as an inhibitor of proliferation, migration and invasion of prostate cancer by targeting E2F5 in prostate cancer cell lines (PMID:27074041)
  • miR-154 was upregulated in CD133(+) Glioblastoma multiforme cell lines. (PMID:27338789)
  • The results suggest that miR-154 downregulation may be involved in glioma formation and progression, and that miR-154 might serve as a potential prognostic biomarker for patients with this disease. (PMID:27417886)
  • targeting of DKK2 by miR-154 leads to upregulation of beta-catenin expression and activation of the classical Wnt signaling pathway and cardiac fibroblasts. (PMID:27542661)
  • Low miR154 expression is associated with Growth and Invasion of Gastric Cancer. (PMID:28800791)
  • Results demonstrate that miR-154-5p is downregulated in glioblastoma and functions as a tumor suppressor, thus regulating glioblastoma cell growth, invasion and migration by targeting PIWIL1 in vitro and in vivo. Findings suggest that miR-154-5p may be a significant potential biomarker for prognosis evaluation and therapeutic procedure in malignant glioblastoma. (PMID:28842123)
  • Data found that miR-154 was downregulated in bladder cancer (BC) tissues and lower miR-154 expression levels were strongly associated with worse overall survival rates of patients with BC. Further study suggested that this was due to decreased inhibition of BC cell proliferation, migration and invasion mediated by miR-154. (PMID:29048677)
  • MiR-154 can inhibit GSK-3beta expression by activating Wnt/beta-catenin signaling pathway, which promotes myocardial fibrosis (PMID:29687862)
  • miR-154 inhibits proliferation and induces apoptosis of human skin SCC cells by down-regulating WHSC1 and blocking the P53 signaling pathway (PMID:29727714)
  • hsa-miR-154-5p, alone or in combination with hsa-miR-196b-5p, hsa-miR-378a-3p and hsa-miR-33a-5p and the clinical parameters of BMI and age, may be applicable for non-invasive diagnosis of the endrometriosis (PMID:29857988)
  • High miR154 expression is associated with renal cell carcinoma. (PMID:30138594)
  • the results of our studies illuminate how SNHG1 formed a regulatory network to confer an oncogenic function in colorectal cancer and suggest that SNHG1 may serve as a potential target for colorectal cancer diagnosis and treatment. (PMID:30266084)
  • miR154 expression was significantly downregulated and negatively correlated with ATG7 expression in bladder cancer (BCa) tissues and cell lines. miR154 expression was associated with advanced T stage, lymphatic invasion, and distant metastasis. A xenograft study revealed that miR154 inhibited BCa cell growth in vivo and suppressed ATG7 expression. (PMID:30483807)
  • Data show that 56% of Bcl2-associated athanogene 3 protein (BAG3+)/ dilated cardiomyopathy (DCM+) significantly co-expressed mir-154-5p and mir-182-5p, suggesting that co-expression of mir-154-5p and mir-182-5p may potentially show diagnostic value. (PMID:30792263)
  • MiR-154 inhibits cells proliferation and metastasis in melanoma by targeting AURKA and serves as a novel prognostic indicator. (PMID:31173299)
  • Oxidative injury in HUVECs was regulated by microRNA-154 targeting the Wnt/ss-catenin signaling pathway. (PMID:31359876)
  • miR-154-3p and miR-487-3p synergistically modulate RHOA signaling in the carcinogenesis of thyroid cancer. (PMID:31820783)
  • Circ_101064 regulates the proliferation, invasion and migration of glioma cells through miR-154-5p/ PIWIL1 axis. (PMID:31941603)
  • Correlation between serum miR-154-5p and urinary albumin excretion rates in patients with type 2 diabetes mellitus: a cross-sectional cohort study. (PMID:31950345)
  • Upregulation of miRNA-154-5p prevents the tumorigenesis of osteosarcoma. (PMID:32000044)
  • Long intergenic non-coding RNA 1939 eliminates proliferation and migration of human renal cell carcinoma (RCC) cells by down-regulation of miR-154. (PMID:32138544)
  • Long non-coding RNA SNHG11 promotes cell proliferation, invasion and migration in glioma by targeting miR-154-5p. (PMID:32432753)
  • Histone deacetylase 1 regulates the malignancy of oral cancer cells via miR-154-5p/PCNA axis. (PMID:32549181)
  • Circular RNA circABCC4 acts as a ceRNA of miR-154-5p to improve cell viability, migration and invasion of breast cancer cells in vitro. (PMID:33023375)
  • SP1 activated-lncRNA SNHG1 mediates the development of epilepsy via miR-154-5p/TLR5 axis. (PMID:33096314)
  • lncRNA DLGAP1-AS2 Knockdown Inhibits Hepatocellular Carcinoma Cell Migration and Invasion by Regulating miR-154-5p Methylation. (PMID:33195697)
  • Circ-ATAD1 is overexpressed in osteosarcoma (OS) and suppresses the maturation of miR-154-5p to increase cell invasion and migration. (PMID:34857012)
  • Exosomes-derived miR-154-5p attenuates esophageal squamous cell carcinoma progression and angiogenesis by targeting kinesin family member 14. (PMID:35156510)
  • LncRNA KCNQ10T1 shuttled by bone marrow mesenchymal stem cell-derived exosome inhibits sepsis via regulation of miR-154-3p/RNF19A axis. (PMID:37326687)
  • MicroRNA-154-5p suppresses cervical carcinoma growth and metastasis by silencing Cullin2 in vitro and in vivo. (PMID:37397007)

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusMir154ENSMUSG00000065448
rattus_norvegicusMir154ENSRNOG00000035600

Paralogs (16): MIR494 (ENSG00000194717), MIR377 (ENSG00000199015), MIR381 (ENSG00000199020), MIR369 (ENSG00000199025), MIR323A (ENSG00000199069), MIR410 (ENSG00000199092), MIR409 (ENSG00000199107), MIR539 (ENSG00000202560), MIR487A (ENSG00000207742), MIR487B (ENSG00000207754), MIR656 (ENSG00000207959), MIR496 (ENSG00000207961), MIR323B (ENSG00000208004), MIR1185-1 (ENSG00000221525), MIR1185-2 (ENSG00000221614), MIR382 (ENSG00000283170)

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.