Tian Jiao, Liu Chaoge, Li Bing, Hu Ning, Gu Xiaoting, Li Dongmei, Ai Xiaoyu, Zhou Honggang, Xiao Ting, Yang Cheng
State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy and Tianjin Key Laboratory of Molecular Drug Research, Department of Oramaxillofacial - Head and Neck Surgery, Tianjin Stomatological Hospital, School of Medicine, Nankai University, Tianjin, People's Republic of China.
Tianjin Key Laboratory of Molecular Drug Research, Tianjin International Joint Academy of Biomedicine, Tianjin, People's Republic of China.
Oncogene. 2025 May 8. doi: 10.1038/s41388-025-03421-0.
Ferroptosis, a cell death mechanism characterized by the accumulation of lipid peroxides and subsequent membrane disruption, is emerging as a promising strategy for cancer treatment. However, many tumors, including head and neck squamous cell carcinoma (HNSCC), show resistance to ferroptosis, which reduces its therapeutic effect. Protease-activated receptors (PARs) are highly expressed in many tumors and are closely associated with tumor progression. Our study showed that the expression of protease-activated receptor 1 (PAR1) was downregulated during ferroptosis in HPV-negative HNSCC. Further studies showed that downregulation of PAR1 expression could enhance the therapeutic effect of Erastin on HPV-negative HNSCC, where PAR1 regulated the expression levels of SLC7A11, GPX4, and FTH1. In addition, we found that PAR1 activated the JAK2/STAT3 pathway in a Rac-1-dependent manner and identified STAT3 as a critical transcription factor in PAR1-mediated HPV-negative HNSCC progression and ferroptosis regulation. Inhibition of STAT3 expression attenuated the tumorigenicity of PAR1. It is worth noting that the PAR1 small molecule inhibitor Vorapaxar can further enhance the therapeutic effect of Erastin on HPV-negative HNSCC. Therefore, we propose that PAR1 participates in the progression of HPV-negative HNSCC through STAT3 and reduces the sensitivity of HPV-negative HNSCC to ferroptosis, providing a new perspective for discovering ferroptosis regulatory factors.
铁死亡是一种以脂质过氧化物积累和随后的膜破坏为特征的细胞死亡机制,正成为一种有前景的癌症治疗策略。然而,包括头颈部鳞状细胞癌(HNSCC)在内的许多肿瘤对铁死亡具有抗性,这降低了其治疗效果。蛋白酶激活受体(PARs)在许多肿瘤中高度表达,且与肿瘤进展密切相关。我们的研究表明,在HPV阴性的HNSCC中,铁死亡过程中蛋白酶激活受体1(PAR1)的表达下调。进一步研究表明,PAR1表达的下调可增强艾拉司群对HPV阴性HNSCC的治疗效果,其中PAR1调节溶质载体家族7成员11(SLC7A11)、谷胱甘肽过氧化物酶4(GPX4)和铁蛋白重链1(FTH1)的表达水平。此外,我们发现PAR1以Rac-1依赖的方式激活Janus激酶2/信号转导和转录激活因子3(JAK2/STAT3)信号通路,并确定STAT3是PAR1介导的HPV阴性HNSCC进展和铁死亡调节中的关键转录因子。抑制STAT3表达可减弱PAR1的致瘤性。值得注意的是,PAR1小分子抑制剂沃拉帕沙可进一步增强艾拉司群对HPV阴性HNSCC的治疗效果。因此,我们提出PAR1通过STAT3参与HPV阴性HNSCC的进展,并降低HPV阴性HNSCC对铁死亡的敏感性,为发现铁死亡调节因子提供了新的视角。