Chadwick Jeffrey W, Macdonald Rachel, Ali Aiman A, Glogauer Michael, Magalhaes Marco A
Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.
Department of Dental Oncology and Maxillofacial Prosthetics, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Front Oncol. 2021 Sep 28;11:741013. doi: 10.3389/fonc.2021.741013. eCollection 2021.
Oral carcinogenesis represents a multi-stage process which encompasses several genetic and molecular changes that promote the progression of oral potentially malignant disorders (OPMDs) to oral squamous cell carcinomas (OSCCs). A better understanding of critical pathways governing the progression of OMPDs to OSCCs is critical to improve oncologic outcomes in the future. Previous studies have identified an important role of tumor necrosis factor α (TNFα) and TNF receptor 1 (TNFR1) in the invasiveness of oral cancer cell lines. Here, we investigate the expression of TNFα and TNFR1 in human OPMDs that progress to OSCC compared to non-progressing OPMDs utilizing fluorescent immunohistochemistry (FIHC) to show increased TNFα/TNFR1 expression in progressing OPMDs. In order to interrogate the TNFα/TNFR1 signaling pathway, we utilized a 4-nitroquinoline 1-oxide (4-NQO) mouse model of oral carcinogenesis to demonstrate that TNFα/TNFR1 expression is upregulated in 4-NQO-induced OSCCs. TNFα neutralization decreased serum cytokines, inhibited the development of invasive lesions and reduced tumor-associated neutrophils . Combined, this data supports the role of TNFα in oral malignant transformation, suggesting that critical immunoregulatory events occur downstream of TNFR1 leading to malignant transformation. Our results advance the understanding of the mechanisms governing OSCC invasion and may serve as a basis for alternative diagnostic and therapeutic approaches to OPMDs and OSCC management.
口腔癌发生是一个多阶段过程,涉及多种基因和分子变化,这些变化促使口腔潜在恶性疾病(OPMD)进展为口腔鳞状细胞癌(OSCC)。更好地了解调控OPMD进展为OSCC的关键途径对于改善未来肿瘤治疗结局至关重要。既往研究已证实肿瘤坏死因子α(TNFα)和肿瘤坏死因子受体1(TNFR1)在口腔癌细胞系侵袭中起重要作用。在此,我们利用荧光免疫组织化学(FIHC)研究进展为OSCC的人OPMD中TNFα和TNFR1的表达,并与未进展的OPMD进行比较,结果显示进展中的OPMD中TNFα/TNFR1表达增加。为了探究TNFα/TNFR1信号通路,我们利用4-硝基喹啉-1-氧化物(4-NQO)口腔癌发生小鼠模型,证明在4-NQO诱导的OSCC中TNFα/TNFR1表达上调。TNFα中和降低了血清细胞因子水平,抑制了侵袭性病变的发展,并减少了肿瘤相关中性粒细胞。综合来看,这些数据支持TNFα在口腔恶性转化中的作用,表明关键的免疫调节事件发生在TNFR1下游,导致恶性转化。我们的结果推进了对OSCC侵袭机制的理解,并可能为OPMD和OSCC管理的替代诊断和治疗方法提供依据。