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Prader-Willi region non-protein coding RNA 2 (PWRN2) is a long non-coding RNA transcribed from the Prader-Willi locus on chromosome 15. It does not encode a protein but rather modulates gene expression via several mechanisms, most notably as a competing endogenous RNA. It has roles in neurodevelopment (regulation of neurodevelopmental gene transcription), in the cellular response to stress (promoting cell death and apoptosis in retinal cells exposed to oxidative injury), and in female reproductive biology (affecting oocyte maturation and metabolic gene regulation in PCOS). PWRN2’s dysregulation has been associated with pathologies such as Prader-Willi syndrome, age-related macular degeneration, and polycystic ovary syndrome. Currently, no drugs target PWRN2 directly, but its expression may serve as a disease biomarker or as a molecular node for future therapeutic RNA interventions[1][2][3][7][8].
No drugs act directly on PWRN2. Its mechanism includes ceRNA function—regulating miRNA availability and thus downstream mRNA translation
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