Department of Otolaryngology, Head and Neck Surgery, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, China (mainland).
Department of Otolaryngology, Head and Neck Surgery, First Affiliated Hospital of Chongqing Medical University, Chongqing, China (mainland).
Med Sci Monit. 2021 Dec 16;27:e931970. doi: 10.12659/MSM.931970.
BACKGROUND Forkhead box protein M1 (FoxM1) is an important transcription factor involved in the development and progression of various malignancies. However, its role in nasopharyngeal carcinoma (NPC) remains largely unknown. This study aimed to assess the effect of FoxM1 on NPC cell tumorigenesis as well as the underlying mechanism. MATERIAL AND METHODS NPC cell lines CNE-1 and CNE-2 were treated with vehicle and FoxM1 inhibitor thiostrepton or transfected with small interfering RNA. CCK-8 assay, flow cytometric assay, and Hoechst 33258 staining were performed to assess the viability, apoptosis and nuclear morphological impairment, and cell cycle, respectively. The expression of apoptosis-related caspase-3 and caspase-9 was detected by western blot analysis The tumor growth in the mouse xenograft model of NPC treated with thiostrepton or control was assessed. The expression of Wnt/ß-catenin signaling proteins p27, FoxM1, S phase kinase-associated protein 2 (SKP2), and Cyclin D1 were determined both in cells and xenograft tissues by western blot analysis. RESULTS Inhibition of FoxM1 by thiostrepton significantly suppressed NPC cell viability, induced apoptosis, increased cell cycle arrest, impaired nuclear morphology, and reduced NPC cell-derived tumor xenograft growth. Mechanistically, inhibition or knockdown of FoxM1 inactivated the Wnt/ß-catenin signaling pathway, as demonstrated by altered expression of Wnt/ß-catenin signaling-related genes, including p27, SKP2, and cyclin D1, in both NPC cells and xenograft tissues. CONCLUSIONS We identified FoxM1 as a novel regulator of NPC cell tumorigenesis in vitro and in vivo. Targeting FoxM1 could be a promising therapeutic strategy against NPC.
叉头框蛋白 M1(FoxM1)是一种重要的转录因子,参与多种恶性肿瘤的发生和发展。然而,其在鼻咽癌(NPC)中的作用仍知之甚少。本研究旨在评估 FoxM1 对 NPC 细胞肿瘤发生的影响及其潜在机制。
用 FoxM1 抑制剂硫链丝菌素或小干扰 RNA 转染 CNE-1 和 CNE-2 NPC 细胞系。用 CCK-8 法、流式细胞术和 Hoechst 33258 染色分别评估细胞活力、细胞凋亡和核形态损伤以及细胞周期。Western blot 分析检测凋亡相关 caspase-3 和 caspase-9 的表达。用硫链丝菌素或对照处理 NPC 荷瘤小鼠模型,评估肿瘤生长情况。Western blot 分析检测细胞和异种组织中 Wnt/β-catenin 信号通路蛋白 p27、FoxM1、S 期激酶相关蛋白 2(SKP2)和细胞周期蛋白 D1 的表达。
硫链丝菌素抑制 FoxM1 显著抑制 NPC 细胞活力,诱导细胞凋亡,增加细胞周期阻滞,损害核形态,并减少 NPC 细胞来源的肿瘤异种移植生长。机制上,FoxM1 的抑制或敲低使 Wnt/β-catenin 信号通路失活,这表现在 NPC 细胞和异种组织中 Wnt/β-catenin 信号相关基因(包括 p27、SKP2 和细胞周期蛋白 D1)的表达改变。
我们确定 FoxM1 是 NPC 细胞体内外肿瘤发生的一种新的调节因子。靶向 FoxM1 可能是一种有前途的 NPC 治疗策略。