| HGNC Family | Non-coding RNAs |
| Name | microRNA 4484 |
| 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": "\nIn glioblastoma, miR‐4484 has been identified as an intragenic microRNA located on chromosome 10 that is frequently deleted and downregulated. Functional investigations demonstrated that restoring miR‐4484 in glioma cells suppresses colony formation and reduces migratory capabilities, indicating its tumor‐suppressive role likely mediated through the regulation of key oncogenic targets involved in gliomagenesis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn contrast, in systemic sclerosis the circulating levels of miR‐4484 are markedly elevated. Bioinformatics analyses suggest that miR‐4484 could regulate critical components of the fibrotic process, including elements of the transforming growth factor‐β signaling pathway, extracellular matrix receptor interactions, and metalloproteinase expression—most notably implicating a potential link with MMP-21—thereby proposing a novel biomarker role in the disease’s pathogenesis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFurthermore, research in gastric cancer reveals that miR‐4484 is significantly downregulated in tumor tissues compared with adjacent normal mucosa. The reduced expression of this miRNA shows an inverse correlation with the upregulation of ITGA6, a direct target of miR‐4484, suggesting that loss of miR‐4484 may contribute to enhanced invasion and metastasis in gastric cancer. These findings highlight miR‐4484 as a potential prognostic marker and therapeutic target in this malignancy."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Zahid Nawaz, Vikas Patil, Sivaarumugam Thinagararjan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Impact of somatic copy number alterations on the glioblastoma miRNome: miR-4484 is a genomically deleted tumour suppressor."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Oncol (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/1878-0261.12060"}], "href": "https://doi.org/10.1002/1878-0261.12060"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28378523"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28378523"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Marta Rusek, Małgorzata Michalska-Jakubus, Małgorzata Kowal, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A novel miRNA-4484 is up-regulated on microarray and associated with increased MMP-21 expression in serum of systemic sclerosis patients."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41598-019-50695-y"}], "href": "https://doi.org/10.1038/s41598-019-50695-y"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31582779"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31582779"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "H Y Zhong, Y Zhong, Y Wen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "[MiR-4484 regulates the expression of integrin α 6 in gastric cancer tissues and its significance]."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Zhonghua Zhong Liu Za Zhi (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3760/cma.j.cn112152-20200404-00305"}], "href": "https://doi.org/10.3760/cma.j.cn112152-20200404-00305"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35316874"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35316874"}]}]}]}
|
| Synonyms | MIR-4484 |
| NCBI Gene ID | 100616327 |
| API | |
| Download Associations | |
| Predicted Functions |
![]() |
| Co-expressed Genes |
![]() |
| Expression in Tissues and Cell Lines |
![]() |
MIR4484 has 241 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 8 datasets.
Click the + buttons to view associations for MIR4484 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CCLE Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR4484 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR4484 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset. | |
| ENCODE Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR4484 gene from the ENCODE Histone Modification Site Profiles dataset. | |
| ENCODE Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR4484 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR4484 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR4484 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| MotifMap Predicted Transcription Factor Targets | transcription factors regulating expression of MIR4484 gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset. | |
| Roadmap Epigenomics Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR4484 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |