The review includes antisense oligonucleotides among the RNA-based therapeutic strategies assessed for multiple myeloma.
First-pass extracted concept
antisense oligonucleotides
Candidate: concept label2 source documents3 linked claims
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Aliases
ASOs
Extracted Explainers
Evidence Snippets
modalities including mRNA vaccines, small interfering RNAs (siRNAs), antisense oligonucleotides (ASOs), and microRNA (miRNA) mimics/inhibitors
the majority of approved OGTs, as well as those currently in clinical trials, are antisense oligonucleotides (ASOs) despite cell culture data showing that small interfering RNAs (siRNAs) exhibit greater potency.
Supporting Sources
Linked Claims
Most approved and clinical-trial oligonucleotide-based gene therapeutics are antisense oligonucleotides even though siRNAs show greater potency in cell culture data.
Quoted textsource-backed
the majority of approved OGTs, as well as those currently in clinical trials, are antisense oligonucleotides (ASOs) despite cell culture data showing that small interfering RNAs (siRNAs) exhibit greater potency.
The review assesses RNA-based therapeutic modalities for multiple myeloma including mRNA vaccines, siRNAs, ASOs, and miRNA mimics or inhibitors using preclinical and clinical evidence.
Quoted textsource-backed
In this review, we assess cutting-edge RNA-based therapeutics for MM modulation, drawing on preclinical and clinical evidence on modalities including mRNA vaccines, small interfering RNAs (siRNAs), antisense oligonucleotides (ASOs), and microRNA (miRNA) mimics/inhibitors.
The review concludes that RNA technologies have transformative potential in refractory multiple myeloma to achieve durable remissions, overcome resistance, reduce costs, and enable more personalized and safer treatments.
Quoted textsource-backed
By integrating these insights, we underscore RNA technologies' transformative potential to achieve durable remissions, overcome resistance, and reduce costs-paving the way for personalized, safer treatments in refractory MM.