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MicroRNA 1304 (MIR1304) is a short (20–24 nt) non-coding RNA classified as a microRNA, involved in the post-transcriptional regulation of gene expression by affecting both the stability and translation of target mRNAs. MIR1304 is transcribed as a primary transcript and processed by Drosha and Dicer enzymes to yield the mature miRNA, which is incorporated into the RNA-induced silencing complex (RISC). The mature MIR1304 can bind imperfectly to complementary sites in target mRNAs to direct their translational inhibition or destabilization. Functionally, miR-1304 has been implicated in various cancers: it acts as a tumor suppressor in non-small cell lung cancer by targeting HO-1 mRNA, promoting cell cycle arrest and apoptosis, and as an oncomiR in breast cancer—especially among African American patients—by targeting the anti-adipogenic gene GATA2 and activating cancer-associated adipocytes to supply lipids for tumor growth. The allele frequency of certain SNPs in the MIR1304 stem-loop structure may underlie differences in maturation rates and contribute to cancer health disparities between ethnic groups. No approved clinical drugs directly target MIR1304 as of now.
Inhibition of specific mRNA targets through RNA-induced silencing complex (RISC), leading to translational repression or mRNA destabilization (e.g., targeting GATA2 and HO-1)
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