| HGNC Family | Non-coding RNAs |
| Name | microRNA 3677 |
| 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": "\nmiR-3677-3p exhibits context‐dependent roles in tumor biology. In human osteosarcoma cells, miR-3677 directly binds to SphK1 mRNA, and its overexpression suppresses cell growth, proliferation, and migration, whereas its inhibition augments these processes—indicating that in this context miR-3677 acts as a tumor suppressor."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn hepatocellular carcinoma (HCC), however, miR-3677-3p is frequently upregulated and associates with poor clinical outcomes. Studies have demonstrated that miR-3677-3p promotes oncogenic behaviors through the direct suppression of tumor suppressor molecules. For example, one study showed that miR-3677-3p downregulates SIRT5, enhancing proliferation, migration, and invasion in HCC cells, particularly under hypoxic conditions."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": " Similarly, another investigation reported that by directly targeting the 3′ untranslated region of GSK3β, miR-3677-3p effectively inhibited its expression and thereby facilitated tumor progression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": " Moreover, in hepatitis B virus–associated HCC, miR-3677-3p contributes to both tumor progression and sorafenib resistance through targeting FBXO31—which normally promotes the ubiquitylation and degradation of the oncogenic transcription factor FOXM1."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn cervical cancer, the oncogenic potential of miR-3677-3p is further highlighted by its interaction with non-coding RNAs. Specifically, the long non-coding RNA TRAF3IP2-AS1 acts as a sponge for miR-3677-3p, thereby mitigating its ability to promote cell proliferation, migration, and invasion. This modulatory mechanism not only underscores the functional relevance of miR-3677-3p in tumor progression but also points to its potential utility as a diagnostic biomarker and therapeutic target."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Chen Yao, Jian-Wei Ruan, Yun-Rong Zhu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The therapeutic value of the SphK1-targeting microRNA-3677 in human osteosarcoma cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Aging (Albany NY) (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.18632/aging.102961"}], "href": "https://doi.org/10.18632/aging.102961"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32203055"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32203055"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Bowen Yao, Yazhao Li, Yongshen Niu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Hypoxia-induced miR-3677-3p promotes the proliferation, migration and invasion of hepatocellular carcinoma cells by suppressing SIRT5."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Mol Med (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/jcmm.15503"}], "href": "https://doi.org/10.1111/jcmm.15503"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32596968"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32596968"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Yanfei Li, Yajie Zhou, Linlin Ma, et al. "}, {"type": "b", "children": [{"type": "t", "text": "miR-3677-3p promotes hepatocellular carcinoma progression via inhibiting GSK3β."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Acta Biochim Biophys Sin (Shanghai) (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/abbs/gmaa125"}], "href": "https://doi.org/10.1093/abbs/gmaa125"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33200777"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33200777"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Hengzheng He, Jian Zhou, Fahui Cheng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-3677-3p promotes development and sorafenib resistance of hepatitis B-related hepatocellular carcinoma by inhibiting FOXM1 ubiquitination."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Cell (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s13577-023-00945-z"}], "href": "https://doi.org/10.1007/s13577-023-00945-z"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37402927"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37402927"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Chuncui Luo, Xixia Pang "}, {"type": "b", "children": [{"type": "t", "text": "IncRNA TRAF3IP2-AS1 Restrains Cervical Cancer Progression by Sponging miR-3677-3p and Acts As a Diagnostic Marker in Cervical Cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Crit Rev Eukaryot Gene Expr (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1615/CritRevEukaryotGeneExpr.2022044035"}], "href": "https://doi.org/10.1615/CritRevEukaryotGeneExpr.2022044035"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "36374810"}], "href": "https://pubmed.ncbi.nlm.nih.gov/36374810"}]}]}]}
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| Synonyms | MIR-3677 |
| NCBI Gene ID | 100500812 |
| 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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MIR3677 has 480 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 9 datasets.
Click the + buttons to view associations for MIR3677 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 MIR3677 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 MIR3677 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 MIR3677 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 MIR3677 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR3677 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| JASPAR Predicted Transcription Factor Targets | transcription factors regulating expression of MIR3677 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR3677 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 MIR3677 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 MIR3677 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |