School of Dentistry, University Center Univates, Lajeado, RS, Brazil.
School of Dentistry, Federal University of Rio Grande do Sul, Porto Alegre, RS, Brazil.
Oral Oncol. 2021 Jan;112:105038. doi: 10.1016/j.oraloncology.2020.105038. Epub 2020 Oct 28.
To analyze the inflammatory millieu in oral squamous cell carcinoma (OSCC) tumors and the influence of macrophages related-cytokines on the tumor cell migration.
Inflammatory protein profile and macrophage population (M2/M1 ratio) of human OSCC fragments were analyzed by proteomic analysis and flow cytometry assay respectively. To evaluate the effects of inflammation on OSCC behavior, we analyzed the role of polarized macrophages and cytokines (IL-6, IL-1β and TNF-α) on OSCC cell lines (SCC25 and Cal27) responsiveness by western blotting (cell signaling) and time-lapse (cell migration). Also, it was addressed the crosstalk of IL-6-STAT3 axis with cell migration signaling using a STAT3 inhibitor (Stattic®) and a pull down assay for the RhoGTPase Rac1 activity.
It was observed a ~2 fold predominance of M2 over M1 macrophages and a pro-inflammatory state in OSCC fragments. The M2 conditioned media increased migration speed and directionality of highly invasive OSCC cells (SCC25). OSCC cell lines were responsive to cytokine stimuli (IL6, IL-1β and TNF-α), but only IL-6 increased migration properties of OSCC cells. This effect was dependent on STAT3-phosphorylation levels, which interfered with Rac1 activation levels.
Our results suggest that the inflammatory milieu might favor invasion and metastasis of OSCC by the direct effect of macrophage-related cytokines on tumor migration.
分析口腔鳞状细胞癌(OSCC)肿瘤中的炎症环境以及巨噬细胞相关细胞因子对肿瘤细胞迁移的影响。
通过蛋白质组学分析和流式细胞术分别分析人 OSCC 片段中的炎症蛋白谱和巨噬细胞群体(M2/M1 比值)。为了评估炎症对 OSCC 行为的影响,我们通过 Western blot(细胞信号转导)和延时拍摄(细胞迁移)分析极化巨噬细胞和细胞因子(IL-6、IL-1β 和 TNF-α)对 OSCC 细胞系(SCC25 和 Cal27)反应的作用。还使用 STAT3 抑制剂(Stattic®)和 RhoGTPase Rac1 活性下拉测定来解决 IL-6-STAT3 轴与细胞迁移信号转导的串扰。
观察到 OSCC 片段中 M2 巨噬细胞比 M1 巨噬细胞多约 2 倍,且呈促炎状态。M2 条件培养基增加了高度侵袭性 OSCC 细胞(SCC25)的迁移速度和方向性。OSCC 细胞系对细胞因子刺激(IL6、IL-1β 和 TNF-α)有反应,但只有 IL-6 增加了 OSCC 细胞的迁移特性。这种作用依赖于 STAT3 磷酸化水平,这会干扰 Rac1 激活水平。
我们的结果表明,炎症环境可能通过巨噬细胞相关细胞因子对肿瘤迁移的直接作用促进 OSCC 的侵袭和转移。