| HGNC Family | Non-coding RNAs |
| Name | microRNA 1587 |
| 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 identified miR‑1587 as a critical mediator in tumor progression. In glioblastoma, exosomes released by glioma‑associated human mesenchymal stem cells carry miR‑1587, which enhances the proliferation and clonogenic capacity of glioma stem‐like cells by downregulating the tumor‑suppressive nuclear receptor corepressor NCOR1. In breast cancer, M2‑polarized macrophages promote cell proliferation and migration by upregulating miR‑1587, which targets and suppresses interferon regulatory factor 7 (IRF7), thereby facilitating tumor progression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn the context of keloids, miR‑1587 is involved in regulating fibroblast behavior. Although miR‑1587 is downregulated in keloid tissues and human skin keloid fibroblasts, treatment with botulinum toxin A restores its expression, which in turn targets and suppresses ZEB2. This molecular modulation leads to inhibited fibroblast proliferation and migration, while promoting apoptosis and autophagy, suggesting a potential therapeutic pathway for keloid treatment."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nMoreover, miR‑1587 has been shown to adopt G‑quadruplex structures that facilitate its interaction with proteins such as CASK. This binding event is associated with the downstream transcriptional and translational downregulation of reelin and p21, indicating that miR‑1587 may play a broader role in modulating intracellular metabolic and transcriptional processes across multiple cancer cell types."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Javier Figueroa, Lynette M Phillips, Tal Shahar, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Exosomes from Glioma-Associated Mesenchymal Stem Cells Increase the Tumorigenicity of Glioma Stem-like Cells via Transfer of miR-1587."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Res (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1158/0008-5472.CAN-16-2524"}], "href": "https://doi.org/10.1158/0008-5472.CAN-16-2524"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28855213"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28855213"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Daoyuan Tu, Jin Dou, Mingkao Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "M2 macrophages contribute to cell proliferation and migration of breast cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Biol Int (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/cbin.11528"}], "href": "https://doi.org/10.1002/cbin.11528"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33325089"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33325089"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Zhanying Hou, Feixiang Fan, Po Liu "}, {"type": "b", "children": [{"type": "t", "text": "BTXA regulates the epithelial-mesenchymal transition and autophagy of keloid fibroblasts via modulating miR-1587/miR-2392 targeted ZEB2."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biosci Rep (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1042/BSR20190679"}], "href": "https://doi.org/10.1042/BSR20190679"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31652445"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31652445"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Lulu Zhang, Jiang Zhou, Ming Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Exploration of the Hsa-miR-1587-Protein Interaction and the Inhibition to CASK."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Mol Sci (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3390/ijms221910716"}], "href": "https://doi.org/10.3390/ijms221910716"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34639058"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34639058"}]}]}]}
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| NCBI Gene ID | 100616251 |
| API | |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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MIR1587 has 85 functional associations with biological entities spanning 1 categories (cell line, cell type or tissue) extracted from 2 datasets.
Click the + buttons to view associations for MIR1587 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of MIR1587 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR1587 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |