Spliceosome-Targeted Therapies Induce dsRNA Responses

In a recent issue of Cell, Bowling et al. describe a mechanism by which spliceosome-targeted therapies result in intron-containing transcripts that form double-stranded RNAs (dsRNAs), thereby activating tumor antiviral signaling (viral mimicry) and downstream adaptive immunity. In a recent issue of...

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Veröffentlicht in:Immunity (Cambridge, Mass.) Mass.), 2021-01, Vol.54 (1), p.11-13
Hauptverfasser: Ishak, Charles A., Loo Yau, Helen, De Carvalho, Daniel D.
Format: Artikel
Sprache:eng
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Zusammenfassung:In a recent issue of Cell, Bowling et al. describe a mechanism by which spliceosome-targeted therapies result in intron-containing transcripts that form double-stranded RNAs (dsRNAs), thereby activating tumor antiviral signaling (viral mimicry) and downstream adaptive immunity. In a recent issue of Cell, Bowling et al. describe a mechanism by which spliceosome-targeted therapies result in intron-containing transcripts that form double-stranded RNAs (dsRNAs), thereby activating tumor antiviral signaling (viral mimicry) and downstream adaptive immunity.
ISSN:1074-7613
1097-4180
DOI:10.1016/j.immuni.2020.12.012