Godsk Stine Høvring, Jensen Caroline Maren Stengaard, Larsen Trine Vilsbøll, Ahrenfeldt Johanne, Gammelgaard Kristine Raaby, Jakobsen Martin Roelsgaard
Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Department of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark.
Front Immunol. 2025 Feb 12;15:1525083. doi: 10.3389/fimmu.2024.1525083. eCollection 2024.
The importance of the cGAS-STING pathway and type I interferon (IFN) in anti-tumor immunity has been widely studied. However, there is limited knowledge about the role of type III IFNs in cancer settings. Type III IFNs, comprising IFNλ1-4, are opposite to type I IFN only expressed by a few cell types, including epithelial cells, and the receptor subunit IFNLR1, is equally only expressed on limited types of cells.
Gene and protein expression of the cGAS-STING signaling pathway was characterized in a series of non-small cell lung cancer (NSCLC) cell lines. Herring-testis DNA stimulation and chemotherapy drugs (doxorubicin and cisplatin) were used to activate the cGAS-STING pathway, and the level of activation was determined by measuring changes in the transcriptomic profile as well as type I and III IFNs by ELISA. Re-expression of IFNLR1 on cancer cell lines was achieved using CRISPR activation (CRISPRa) followed by evaluating chemotherapy-induced apoptosis using flow cytometry assays.
STING was not broadly expressed across the NSCLC cell lines. Those cancer cell lines expressing all relevant factors supporting the cGAS-STING pathway secreted IFNλ following STING activation whereas only few of them expressed IFNβ. Treatment with chemotherapy drugs likewise preferentially induced IFNλ, which was abrogated in CRISPR-Cas9 STING knock-out cells. Expression of IFNLR1 was found downregulated in the cancer cell lines compared to the benign epithelial cell line Nuli-1. Rescuing IFNLR1 expression by CRISPRa in multiple cancer cell lines sensitization them to IFNλ-stimulation and resulted in significant reduction in cell viability.
Downregulation of IFNLR1 can be an immune evasion mechanism developed by cancer cells to avoid responding to endogenous type III IFNs. Thus, rescuing IFNLR1 expression in NSCLC in conjunction to chemotherapy may potentially be harnessed to elevate the anti-tumoral responses.
cGAS-STING通路和I型干扰素(IFN)在抗肿瘤免疫中的重要性已得到广泛研究。然而,关于III型IFN在癌症环境中的作用,人们了解有限。III型IFN由IFNλ1-4组成,与仅由少数细胞类型(包括上皮细胞)表达的I型IFN相反,其受体亚基IFNLR1同样仅在有限类型的细胞上表达。
在一系列非小细胞肺癌(NSCLC)细胞系中对cGAS-STING信号通路的基因和蛋白表达进行了表征。使用鲱鱼精巢DNA刺激和化疗药物(阿霉素和顺铂)激活cGAS-STING通路,并通过测量转录组谱的变化以及通过ELISA检测I型和III型IFN来确定激活水平。使用CRISPR激活(CRISPRa)在癌细胞系上重新表达IFNLR1,然后使用流式细胞术检测评估化疗诱导的细胞凋亡情况。
STING在NSCLC细胞系中并非广泛表达。那些表达支持cGAS-STING通路的所有相关因子的癌细胞系在STING激活后分泌IFNλ,而其中只有少数表达IFNβ。化疗药物治疗同样优先诱导IFNλ,这在CRISPR-Cas9 STING敲除细胞中被消除。与良性上皮细胞系Nuli-1相比,发现癌细胞系中IFNLR1的表达下调。通过CRISPRa在多个癌细胞系中挽救IFNLR1表达使其对IFNλ刺激敏感,并导致细胞活力显著降低。
IFNLR1的下调可能是癌细胞为避免对内源性III型IFN产生反应而形成的一种免疫逃逸机制。因此,在NSCLC中联合化疗挽救IFNLR1表达可能有潜力增强抗肿瘤反应。