| HGNC Family | Non-coding RNAs |
| Name | microRNA 4733 |
| 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 uncovered that miR-4733-5p is significantly upregulated in gallbladder carcinoma (GBC), a highly aggressive cancer associated with poor prognosis, and that this miRNA plays a critical role in promoting the proliferation and invasion of GBC cells. The increased expression of miR-4733-5p was validated using GEO dataset analyses, RT-qPCR, ISH staining, and immunohistochemistry, which collectively indicate its involvement in tumor progression by enhancing cell growth and metastasis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "Mechanistically, miR-4733-5p exerts its oncogenic effects by directly binding to the 3′ untranslated region (UTR) of the mRNA encoding the tumor suppressor kruppel‐like factor 7 (KLF7). This interaction leads to the downregulation of KLF7, which normally acts to inhibit GBC cell proliferation and migration; thus, loss of KLF7 function removes a critical brake on tumor development."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "A comprehensive suite of in vitro functional assays—including CCK-8, colony formation, wound healing, and transwell invasion assays—along with xenograft tumor models in vivo, substantiated the role of miR-4733-5p in advancing GBC tumor growth. These findings suggest that targeting miR-4733-5p may provide therapeutic value for managing gallbladder carcinoma by restoring the expression and function of KLF7."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Xiaoqiang Hu, Junzhe Zhang, Junfeng Bu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-4733-5p promotes gallbladder carcinoma progression via directly targeting kruppel like factor 7."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Bioengineered (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/21655979.2022.2065951"}], "href": "https://doi.org/10.1080/21655979.2022.2065951"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35443866"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35443866"}]}]}]}
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| NCBI Gene ID | 100616266 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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MIR4733 has 1,054 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 10 datasets.
Click the + buttons to view associations for MIR4733 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 MIR4733 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| ChEA Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR4733 gene from the CHEA Transcription Factor Binding Site Profiles dataset. | |
| ChEA Transcription Factor Targets | transcription factors binding the promoter of MIR4733 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR4733 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 MIR4733 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 MIR4733 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR4733 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 MIR4733 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 MIR4733 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 MIR4733 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |