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Inhibition of oncogenic protein production at the RNA level encompasses therapeutic strategies aimed at preventing the synthesis of cancer-promoting proteins by targeting their precursor RNA molecules. This approach disrupts the flow of genetic information from DNA to protein, intervening after transcription but before or during translation, thereby reducing or eliminating the production of harmful proteins that drive tumor growth and survival. Key modalities include RNA interference (RNAi) using siRNAs or shRNAs, antisense oligonucleotides (ASOs), microRNAs (miRNAs), and CRISPR-based technologies. Efficient delivery using nanoparticle carriers is crucial for stability and targeted delivery. Notable targets include MYC and NOVA1.
Post-transcriptional gene silencing via siRNA/shRNA/RNAi/ASO/miRNA/sgRNA, leading to mRNA degradation or translation inhibition.
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