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RNA sensing induced by chromosome missegregation augments anti-tumor immunity II

ABSTRACT: RNA sensing induced by chromosome missegregation augments anti-tumor immunity II

PROVIDER: PRJNA1183422 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR31277033_1.fastq.gz	Fastqsanger.gz
	SRR31277033_2.fastq.gz	Fastqsanger.gz
	SRR31277034_1.fastq.gz	Fastqsanger.gz
	SRR31277034_2.fastq.gz	Fastqsanger.gz
	SRR31277035_1.fastq.gz	Fastqsanger.gz

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Project description:We demonstrate that dsRNA is significantly accumulated in cancer cells following pharmacologic induction of micronuclei, stimulating MAVS-mediated dsRNA sensing in conjunction with the cGAS/STING pathway. Activation of cytosolic dsRNA sensing co-operates with dsDNA sensing to up-regulate immune cell migration and antigen-presenting machinery. Tracing of dsRNA-sequence identity revealed that dsRNA-forming transcripts are predominantly generated from non-exonic regions, particularly in locations proximal to genes exhibiting high chromatin accessibility. Activation of this pathway by pulsed Monopolar Spindle 1 (MPS1) kinase inhibitor therapy, which potently induces micronuclei formation, thus induces cytoplasmic dsRNA-sensing and promotes anti-tumor immunity mediated by type I interferon signaling and cytotoxic lymphocyte activation in vivo. Taken together, these findings reveal a novel aspect of the dsRNA-sensing pathway in enhancing the anti-tumor efficacy of drugs that promote genomic instability and micronuclei formation, facilitating cancer immunogenicity.

2024-11-12 | GSE281352 | GEO