Academic Journal

Type I interferon regulation by USP18 is a key vulnerability in cancer

التفاصيل البيبلوغرافية
العنوان: Type I interferon regulation by USP18 is a key vulnerability in cancer
المؤلفون: Jové, V, Wheeler, H, Lee, CW, Healy, DR, Levine, K, Ralph, EC, Yamaguchi, M, Jiang, ZK, Cabral, E, Xu, Y, Stock, J, Yang, B, Giddabasappa, A, Loria, P, Casimiro-Garcia, A, Kessler, BM, Pinto-Fernández, A, Frattini, V, Wes, PD, Wang, F
بيانات النشر: Cell Press
سنة النشر: 2024
المجموعة: Oxford University Research Archive (ORA)
الوصف: Precise regulation of Type I interferon signaling is crucial for combating infection and cancer while avoiding autoimmunity. Type I interferon signaling is negatively regulated by USP18. USP18 cleaves ISG15, an interferon-induced ubiquitin-like modification, via its canonical catalytic function, and inhibits Type I interferon receptor activity through its scaffold role. USP18 loss-of-function dramatically impacts immune regulation, pathogen susceptibility, and tumor growth. However, prior studies have reached conflicting conclusions regarding the relative importance of catalytic versus scaffold function. Here, we develop biochemical and cellular methods to systematically define the physiological role of USP18. By comparing a patient-derived mutation impairing scaffold function (I60N) to a mutation disrupting catalytic activity (C64S), we demonstrate that scaffold function is critical for cancer cell vulnerability to Type I interferon. Surprisingly, we discovered that human USP18 exhibits minimal catalytic activity, in stark contrast to mouse USP18. These findings resolve human USP18's mechanism-of-action and enable USP18-targeted therapeutics.
نوع الوثيقة: article in journal/newspaper
اللغة: English
Relation: https://ora.ox.ac.uk/objects/uuid:cefcfa74-68da-4d22-bf8e-7eede79c810d; https://doi.org/10.1016/j.isci.2024.109593
DOI: 10.1016/j.isci.2024.109593
الاتاحة: https://doi.org/10.1016/j.isci.2024.109593
https://ora.ox.ac.uk/objects/uuid:cefcfa74-68da-4d22-bf8e-7eede79c810d
Rights: info:eu-repo/semantics/openAccess ; CC Attribution-NonCommercial-NoDerivatives (CC BY-NC-ND)
رقم الانضمام: edsbas.67384F66
قاعدة البيانات: BASE
الوصف
DOI:10.1016/j.isci.2024.109593