Anhui Medical College, Hefei, China.
Fuyang Vocational Technical College, Fuyang, China.
Braz J Med Biol Res. 2020;53(6):e8694. doi: 10.1590/1414-431x20208694. Epub 2020 May 8.
Head and neck squamous cell carcinoma (HNSCC) is one of the most common malignant tumors. Ethanol extract of Antrodia cinnamomea (EEA) has been widely studied for its health benefits including anticancer effects. The purpose of this study was to assess the effects of EEA on HNSCC. Cell proliferation, transwell, and wound healing assays were performed. The impact of EEA on tumor growth was investigated using a xenograft model. Expressions of migration-related proteins (MMP-2, MMP-9, TIMP-1, and TIMP-2) and apoptosis-related proteins (cleaved caspase-9 and cleaved PARP) were determined using western blot analysis. The results indicated that EEA significantly inhibited the capacities of proliferation, invasion, and migration of HNSCC cells in a dose-dependent manner. Cleaved caspase-9 and cleaved PARP expressions were increased in cells treated with an increasing concentration of EEA, which suggested that EEA induced apoptosis of HNSCC. MMP-2 and MMP-9 were downregulated when cells were administered EEA, while TIMP-1 and TIMP-2 were not affected, which uncovered the mechanisms mediating the EEA-induced inhibition on cell invasion and migration. The animal experiment also suggested that EEA inhibited tumor growth. Our study confirmed the inhibitive effects of EEA on cell proliferation, invasion, and migration of HNSCC in vitro and in vivo, providing the basis for further study of the application of EEA as an effective candidate for cancer treatment.
头颈部鳞状细胞癌(HNSCC)是最常见的恶性肿瘤之一。樟芝的乙醇提取物(EEA)已被广泛研究,因其具有多种健康益处,包括抗癌作用。本研究旨在评估 EEA 对头颈部鳞状细胞癌的影响。进行了细胞增殖、Transwell 和划痕愈合测定。使用异种移植模型研究了 EEA 对肿瘤生长的影响。通过 Western blot 分析测定迁移相关蛋白(MMP-2、MMP-9、TIMP-1 和 TIMP-2)和凋亡相关蛋白(cleaved caspase-9 和 cleaved PARP)的表达。结果表明,EEA 以剂量依赖性方式显著抑制 HNSCC 细胞的增殖、侵袭和迁移能力。随着 EEA 浓度的增加,细胞中 cleaved caspase-9 和 cleaved PARP 的表达增加,表明 EEA 诱导了 HNSCC 的细胞凋亡。当用 EEA 处理细胞时,MMP-2 和 MMP-9 的表达下调,而 TIMP-1 和 TIMP-2 不受影响,揭示了介导 EEA 诱导的细胞侵袭和迁移抑制的机制。动物实验也表明 EEA 抑制了肿瘤的生长。本研究证实了 EEA 在体外和体内抑制 HNSCC 细胞增殖、侵袭和迁移的作用,为进一步研究 EEA 作为癌症治疗有效候选物的应用提供了依据。