| Literature DB >> 26317465 |
David Roulois1, Helen Loo Yau2, Rajat Singhania1, Yadong Wang1, Arnavaz Danesh1, Shu Yi Shen1, Han Han3, Gangning Liang3, Peter A Jones3, Trevor J Pugh2, Catherine O'Brien4, Daniel D De Carvalho5.
Abstract
DNA-demethylating agents have shown clinical anti-tumor efficacy via an unknown mechanism of action. Using a combination of experimental and bioinformatics analyses in colorectal cancer cells, we demonstrate that low-dose 5-AZA-CdR targets colorectal cancer-initiating cells (CICs) by inducing viral mimicry. This is associated with induction of dsRNAs derived at least in part from endogenous retroviral elements, activation of the MDA5/MAVS RNA recognition pathway, and downstream activation of IRF7. Indeed, disruption of virus recognition pathways, by individually knocking down MDA5, MAVS, or IRF7, inhibits the ability of 5-AZA-CdR to target colorectal CICs and significantly decreases 5-AZA-CdR long-term growth effects. Moreover, transfection of dsRNA into CICs can mimic the effects of 5-AZA-CdR. Together, our results represent a major shift in understanding the anti-tumor mechanisms of DNA-demethylating agents and highlight the MDA5/MAVS/IRF7 pathway as a potentially druggable target against CICs.Entities:
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Year: 2015 PMID: 26317465 PMCID: PMC4843502 DOI: 10.1016/j.cell.2015.07.056
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582