Sun Yujuan, Liu Nan, Guan Xiaobing, Wu Hongru, Sun Zheng, Zeng Hui
Department of Periodontal & Oral Medicine, Beijing Stomatological Hospital, Capital Medical University, Beijing 100050, China.
Department of Stomatology, Beijing Tongren Hospital, Capital Medical University, Beijing 100005, China.
Mediators Inflamm. 2016;2016:5715719. doi: 10.1155/2016/5715719. Epub 2016 Dec 8.
Oral squamous cell carcinoma (OSCC) is an aggressive, invasive malignancy of epithelial origin. The progression from premalignant lesions-oral leukoplakia (OLK) and oral lichen planus (OLP)-to OSCC involves complex inflammatory processes that have not been elucidated. We investigated the roles of inflammatory mediators and infiltrating immunocytes in the pathogenic progression of OLK and OLP to OSCC. The occurrence of regulatory T-cells (Tregs) and tumor-associated macrophages (TAMs) and the expression of anti-inflammatory cytokines and proinflammatory cytokines were investigated in OLK, OLP, and OSCC tissues. Immunohistochemical staining of CD4, FOXP3, CD68, TGF-1, IL-10, IL-4, IFN-, and MCP-1 showed that the occurrence of Tregs and TAMs increased in parallel with disease progression in OLK and OSCC. IL-10 gradually increased during the early stages of OLK and in OSCC. Infiltrating IL-4 macrophages were seen with increasing frequency in OLK tissue during the progression of oral dysplasia. Fewer TGF-1 macrophages were seen in OSCC than in OLK and OLP. The expression of IFN- decreased gradually with the OLK development and had the lowest expression in OSCC. MCP-1 expression did not change significantly during the development of OSCC. The results suggested that the immunosuppression induced by chronic inflammation promotes tumorigenesis in OSCC, rather than initiating it.
口腔鳞状细胞癌(OSCC)是一种侵袭性的上皮源性恶性肿瘤。从癌前病变——口腔白斑(OLK)和口腔扁平苔藓(OLP)发展到OSCC的过程涉及尚未阐明的复杂炎症过程。我们研究了炎症介质和浸润免疫细胞在OLK和OLP向OSCC致病进展中的作用。在OLK、OLP和OSCC组织中研究了调节性T细胞(Tregs)和肿瘤相关巨噬细胞(TAMs)的发生情况以及抗炎细胞因子和促炎细胞因子的表达。对CD4、FOXP3、CD68、TGF-1、IL-10、IL-4、IFN-和MCP-1进行免疫组织化学染色显示,Tregs和TAMs的发生与OLK和OSCC中的疾病进展平行增加。IL-10在OLK早期和OSCC中逐渐增加。在口腔发育异常进展过程中,OLK组织中浸润的IL-4巨噬细胞出现频率增加。与OLK和OLP相比,OSCC中TGF-1巨噬细胞较少。随着OLK的发展,IFN-的表达逐渐降低,在OSCC中表达最低。在OSCC发展过程中,MCP-1表达没有显著变化。结果表明,慢性炎症诱导的免疫抑制促进了OSCC的肿瘤发生,而非启动肿瘤发生。