Department of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Integrated Biomedical Sciences Program, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
JCI Insight. 2020 Jun 18;5(12):136720. doi: 10.1172/jci.insight.136720.
Interferon regulatory factor 1 (IRF1) regulates diverse biological functions, including modulation of cellular responses involved in tumorigenesis. Genetic mutations and altered IRF1 function are associated with several cancers. Although the function of IRF1 in the immunobiology of cancer is emerging, IRF1-specific mechanisms regulating tumorigenesis and tissue homeostasis in vivo are not clear. Here, we found that mice lacking IRF1 were hypersusceptible to colorectal tumorigenesis. IRF1 functions in both the myeloid and epithelial compartments to confer protection against AOM/DSS-induced colorectal tumorigenesis. We further found that IRF1 also prevents tumorigenesis in a spontaneous mouse model of colorectal cancer. The attenuated cell death in the colons of Irf1-/- mice was due to defective pyroptosis, apoptosis, and necroptosis (PANoptosis). IRF1 does not regulate inflammation and the inflammasome in the colon. Overall, our study identified IRF1 as an upstream regulator of PANoptosis to induce cell death during colitis-associated tumorigenesis.
干扰素调节因子 1(IRF1)调节多种生物学功能,包括调节肿瘤发生过程中涉及的细胞反应。遗传突变和 IRF1 功能改变与多种癌症有关。尽管 IRF1 在癌症的免疫生物学中的作用正在显现,但在体内调节肿瘤发生和组织稳态的 IRF1 特异性机制尚不清楚。在这里,我们发现缺乏 IRF1 的小鼠易发生结直肠肿瘤发生。IRF1 在髓系和上皮细胞中均发挥作用,以防止 AOM/DSS 诱导的结直肠肿瘤发生。我们进一步发现,IRF1 还可以防止自发性结直肠癌小鼠模型中的肿瘤发生。Irf1-/- 小鼠结肠中减弱的细胞死亡是由于细胞焦亡、细胞凋亡和坏死性凋亡(PANoptosis)缺陷所致。IRF1 不调节结肠中的炎症和炎性小体。总的来说,我们的研究确定了 IRF1 作为 PANoptosis 的上游调节剂,以在结肠炎相关肿瘤发生过程中诱导细胞死亡。