4.3 Article

Cancer therapies activate RIG-I-like receptor pathway through endogenous non-coding RNAs

期刊

ONCOTARGET
卷 7, 期 18, 页码 26496-26515

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.8420

关键词

ionizing radiation; DNA damage; small non-coding RNAs; type I interferon; RIG-I-like receptor (RLR)

资金

  1. Human Tissue Resource Center at the University of Chicago [P30CA014599]
  2. Ludwig Center for Metastasis Research
  3. Ludwig Foundation for Cancer Research
  4. Lung Cancer Research Foundation
  5. Prostate Cancer Research Foundation
  6. Biological Sciences Division
  7. Institute for Translational Medicine/CTSA (NIH) at the University of Chicago [UL1 RR024999]

向作者/读者索取更多资源

Emerging evidence indicates that ionizing radiation (IR) and chemotherapy activate Type I interferon (IFN) signaling in tumor and host cells. However, the mechanism of induction is poorly understood. We identified a novel radioprotective role for the DEXH box RNA helicase LGP2 (DHX58) through its suppression of IR-induced cytotoxic IFN-beta [1]. LGP2 inhibits activation of the RIG-I-like receptor (RLR) pathway upon binding of viral RNA to the cytoplasmic sensors RIG-I (DDX58) and MDA5 (IFIH1) and subsequent IFN signaling via the mitochondrial adaptor protein MAVS (IPS1). Here we show that MAVS is necessary for IFN-beta induction and interferon-stimulated gene expression in the response to IR. Suppression of MAVS conferred radioresistance in normal and cancer cells. Germline deletion of RIG-I, but not MDA5, protected mice from death following total body irradiation, while deletion of LGP2 accelerated the death of irradiated animals. In human tumors depletion of RIG-I conferred resistance to IR and different classes of chemotherapy drugs. Mechanistically, IR stimulated the binding of cytoplasmic RIG-I with small endogenous non-coding RNAs (sncRNAs), which triggered IFN-beta activity. We demonstrate that the small nuclear RNAs U1 and U2 translocate to the cytoplasm after IR treatment, thus stimulating the formation of RIG-I: RNA complexes and initiating downstream signaling events. Taken together, these findings suggest that the physiologic responses to radio-/chemo-therapy converge on an antiviral program in recruitment of the RLR pathway by a sncRNA-dependent activation of RIG-I which commences cytotoxic IFN signaling. Importantly, activation of interferon genes by radiation or chemotherapy is associated with a favorable outcome in patients undergoing treatment for cancer. To our knowledge, this is the first demonstration of a cell-intrinsic response to clinically relevant genotoxic treatments mediated by an RNA-dependent mechanism.

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