MIR885 is a microRNA implicated in various cellular processes and has been observed in peak-calling annotation alongside other genes at the 5'UTR region [PMC6356444]. Its expression was found to be decreased in sFRP4 SI cells but was upregulated four-fold in sFRP4 OE cells compared to control U87 cells [PMC6356444]. MIR885 is linked to the p53 pathway and has been localized in the cytoplasm, as demonstrated by in situ hybridization [PMC6356444]. It plays a role in autophagy, acting as a negative regulator by targeting various autophagy-related genes [PMC4990999]. MIR885 has also been associated with cellular migration, where its upregulation stimulates migration and downregulates IGFBP-5 [PMC9203274]. It is expressed under the control of the CMV promoter and can suppress ISRE activities induced by IFN-α stimulation [PMC3434395]. Furthermore, MIR885 interacts with p73ΔEx2/3 to enhance stemness and self-renewal capacity in melanoma cells [PMC7765507], while its expression can be influenced by differential methylation of CG dinucleotides within its promoter region [PMC9847511]. Lastly, MIR885 has been identified as a potential tumor suppressor with brain/cerebellum-restricted expression that targets IGFR [PMC8506118].
-- ca c A - cu ccg cucu UCCAUUACACU CC CUGCCUCUu c ||| |||| ||||||||||| || ||||||||| ggc gagA AGGUGAUGUGG GG GACGGAgag c ug ac U - C ua
Disease | Description | Category | PubMed ID |
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Accession | MIMAT0004947 |
Description | Homo sapiens hsa-miR-885-5p mature miRNA |
Sequence | 11 - UCCAUUACACUACCCUGCCUCU - 32 |
Evidence |
experimental
cloned [2] |
Database links |
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Predicted targets |
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Accession | MIMAT0004948 |
Description | Homo sapiens hsa-miR-885-3p mature miRNA |
Sequence | 43 - AGGCAGCGGGGUGUAGUGGAUA - 64 |
Evidence |
experimental
cloned [2] |
Database links |
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Predicted targets |
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