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Updated: Feb 5, 2026

Production, Crystallization, and Structure Determination of the IKK-binding Domain of NEMO
Published on: December 28, 2019
Roles for the IKK-Related Kinases TBK1 and IKKε in Cancer
Joel K Durand1,2, Qing Zhang3,4, Albert S Baldwin5,6
1Curriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. joel_durand@med.unc.edu.
Abstract:
While primarily studied for their roles in innate immune response, the IκB kinase (IKK)-related kinases TANK-binding kinase 1 (TBK1) and IKKε also promote the oncogenic phenotype in a variety of cancers. Additionally, several substrates of these kinases control proliferation, autophagy, cell survival, and cancer immune responses. Here we review the involvement of TBK1 and IKKε in controlling different cancers and in regulating responses to cancer immunotherapy.
Insights
The IκB kinase (IKK)-related kinases, TBK1 and IKKε, are crucial in cancer development and immune responses. This review explores their roles in various cancers and cancer immunotherapy.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- TANK-binding kinase 1 (TBK1) and IKKε are primarily known for their roles in innate immunity.
- These kinases also play significant roles in promoting cancer development and progression.
- Their substrates regulate key cellular processes including proliferation, autophagy, and cell survival.
Purpose of the Study:
- To review the involvement of TBK1 and IKKε in the development and progression of various cancers.
- To examine the role of TBK1 and IKKε in regulating the immune response to cancer.
- To discuss the implications of these kinases in cancer immunotherapy.
Main Methods:
- Literature review of studies on TBK1 and IKKε in cancer.
- Analysis of kinase substrates and their functions in cancer cells.
- Examination of preclinical and clinical data regarding TBK1/IKKε and immunotherapy response.
Main Results:
- TBK1 and IKKε promote oncogenic phenotypes across diverse cancer types.
- These kinases influence cancer cell proliferation, survival, and autophagy.
- Dysregulation of TBK1/IKKε impacts anti-cancer immune responses and immunotherapy efficacy.
Conclusions:
- TBK1 and IKKε are critical regulators of cancer, extending beyond their innate immune functions.
- Targeting TBK1 and IKKε presents a potential therapeutic strategy for various cancers.
- Understanding their role is vital for improving cancer immunotherapy outcomes.
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