Department of Thoracic and Cardiovascular Surgery, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, P.R. China.
Department of Hematology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, P.R. China.
Mol Med Rep. 2017 Dec;16(6):8900-8906. doi: 10.3892/mmr.2017.7680. Epub 2017 Oct 2.
Lung cancer is considered to be a serious disease that poses a significant threat to human health. 2,3,5,4‑tetrahydroxy diphenylethylene‑2‑O‑glucoside (THSG) is a bioactive compound derived from Polygonum multiflorum Thunb. That has been demonstrated to possess antioxidative, anti‑inflammatory and antitumor activities. However, little is currently known regarding the potential anticancer effects of this compound in lung cancer. Therefore, the present study aimed to investigate the effects of THSG on the adhesion and invasion of A549 human lung cancer cells in vitro, and to identify the putative mechanisms involved. Cell Counting kit‑8 assay was performed to determine A549 cell viability following treatment with various doses (0, 5, 10, 25, 50, 100, 150 and 200 µM) of THSG for 12, 24 and 48 h. In addition, cell adhesion and invasion were determined following treatment of A549 cells with 0, 10, 25 or 50 µM THSG for 1, 2 or 3 h, respectively. Reverse transcription‑quantitative polymerase chain reaction analysis was performed to examine the mRNA expression levels of Snail, E‑cadherin, vimentin, matrix metalloproteinase (MMP) 2 and MMP9 following THSG treatment for 12 h. Western blot analysis was conducted to detect the protein expression levels of Snail, E‑cadherin, vimentin, MMP2 and MMP9 following THSG treatment for 24 h. Treatment with THSG (10, 25 and 50 µM) significantly suppressed the adhesion and invasion of A549 human lung cancer cells in a dose‑dependent manner. In addition, the mRNA and protein expression levels of adhesion and invasion‑associated factors were decreased significantly in A549 cells treated with THSG. In conclusion, THSG effectively suppressed the adhesion and invasion of human lung cancer cells potentially by inhibiting the expression of adhesion and invasion‑related genes.
肺癌被认为是一种严重的疾病,对人类健康构成重大威胁。2,3,5,4-四羟基二苯乙烯-2-O-葡萄糖苷(THSG)是一种从何首乌中提取的生物活性化合物,已被证明具有抗氧化、抗炎和抗肿瘤活性。然而,目前关于该化合物在肺癌中的潜在抗癌作用知之甚少。因此,本研究旨在探讨 THSG 对 A549 人肺癌细胞体外黏附和侵袭的影响,并鉴定潜在的作用机制。采用细胞计数试剂盒-8 法检测不同剂量(0、5、10、25、50、100、150 和 200 μM)THSG 处理 A549 细胞 12、24 和 48 h 后的细胞活力。此外,分别用 0、10、25 或 50 μM THSG 处理 A549 细胞 1、2 或 3 h 后,检测细胞黏附和侵袭。用逆转录-定量聚合酶链反应分析 THSG 处理 12 h 后 Snail、E-钙黏蛋白、波形蛋白、基质金属蛋白酶(MMP)2 和 MMP9 的 mRNA 表达水平。用 Western blot 分析 THSG 处理 24 h 后 Snail、E-钙黏蛋白、波形蛋白、MMP2 和 MMP9 的蛋白表达水平。THSG(10、25 和 50 μM)处理显著抑制 A549 人肺癌细胞的黏附和侵袭,呈剂量依赖性。此外,THSG 处理的 A549 细胞中与黏附和侵袭相关的因子的 mRNA 和蛋白表达水平显著降低。综上所述,THSG 通过抑制黏附和侵袭相关基因的表达,有效抑制人肺癌细胞的黏附和侵袭。