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Cited by 566

The DOI matches its Crossref record; 63 of the 63 references it cites were found in a registry or an index.

TBK1 recruitment to STING activates both IRF3 and NF-κB that mediate immune defense against tumors and viral infections

Open access
Yum, Seoyun, Li, Minghao, Fang, Yan, Chen, Zhijian J.·2021·Proceedings of the National Academy of Sciences

Abstract

Significance: The cGAS-STING pathway is important for immune defense against infection and cancer. STING activation triggers multiple signaling cascades leading to activation of IRF3, NF-κB, and autophagy. By generating mice harboring mutations of STING that specifically inactivate different signaling cascades, we found that ablation of IRF3 activation, which is essential for the induction of type I interferons, was not sufficient to abolish the immune defense against virus infection and cancer in mouse models. Rather, impairing the ability of STING to recruit TBK1, which is important for activating both IRF3 and NF-κB, abolished the immune defense functions of STING. These results demonstrate that the recruitment of TBK1 to STING has functions that are broader than activating IRF3 and inducing type I interferons.

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Metadata

Authors
Yum, S., Li, M., Fang, Y., & Chen, Z. J.
Venue
Proceedings of the National Academy of Sciences
Published
2021-03-30
Volume
118
Issue
14
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W3151167688
Cited by
566
References
63
FWCI
23.58
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: TBK1 recruitment to STING activates both IRF3 and NF-κB that mediate immune defense against tumors and viral infections. https://app.cochat.ai/papers/10.1073/pnas.2100225118
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Yum, S., Li, M., Fang, Y., & Chen, Z. J. (2021). TBK1 recruitment to STING activates both IRF3 and NF-κB that mediate immune defense against tumors and viral infections. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.2100225118

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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