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miR-22 is an endogenous, evolutionarily conserved microRNA of approximately 22 nucleotides in length, involved in the post-transcriptional regulation of gene expression by binding to the 3' UTR of target mRNAs. It acts as both a tumor suppressor and, in some contexts, an oncogene depending on the specific cellular environment. miR-22 regulates cancer cell proliferation, senescence, migration, invasion, metastasis, apoptosis, and epithelial-mesenchymal transition by targeting several genes, notably including histone deacetylase 4 (HDAC4), Myc Binding Protein (MYCBP), metadherin (MTDH), matrix metalloproteinase 14 (MMP14), and Snail. Overexpression or modulation of miR-22 has shown potential in preclinical models to inhibit tumor growth and metastasis, highlighting it as a candidate RNA therapeutic and cancer biomarker. As of now, miR-22 is chiefly an experimental molecule, and not yet an approved drug therapy[1][2][3][4].
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