Feng Xiao-Ling, Fei Hui-Zhi, Hu Ling
Department of Anatomy, Chongqing Engineering Research Center of Antitumor Natural Drugs, Chongqing Three Gorges Medical College, Chongqing 404120, P.R. China.
Department of Pharmacology, Chongqing Engineering Research Center of Antitumor Natural Drugs, Chongqing Three Gorges Medical College, Chongqing 404120, P.R. China.
Oncol Lett. 2018 Mar;15(3):2801-2806. doi: 10.3892/ol.2017.7696. Epub 2017 Dec 27.
Lung cancers are the most commonly diagnosed malignant tumors, and are one of the leading causes of morbidity and mortality worldwide. Dexamethasone (DEX) serves an important function in the regulation of lung cancer cell proliferation; however, the mechanisms involved still remain unknown. In the present study, the effects of DEX on A549 cell proliferation and apoptosis were examined, in addition to the potential downstream regulatory mechanisms underlying these effects. A549 cells were treated with different concentrations of DEX at 12, 24 and 48 h time points, followed by the addition of SB431542, an inhibitor of the TGF-β1 receptor, to block the TGF-β1 signaling pathway. Cell proliferation was analyzed using a 3-(4,5-diethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt. The apoptosis rate was measured by Hoechst 33342 and Annexin V/propidium iodide staining and the expression of transforming growth factor (TGF)-β1, Smad family member 2 (Smad2) and caspase-3 were assessed by western blot. The results from the present study demonstrated that the proliferation of A549 cells decreased and the apoptosis rate significantly increased following DEX treatment (P<0.05). Furthermore, the expression of TGF-β1, Smad2 and caspase-3 were significantly increased following DEX stimulation (P<0.05), the effects of which were abrogated by the addition of the TGF-β1 receptor inhibitor, SB431542 (P<0.05). DEX-induced apoptosis in A549 cells, and this effect was abrogated by SB431542, an inhibitor of TGF-β1 receptor signaling, which indicated that the TGF-β1/Smad2 pathway may be associated with this process and SB431542 may function as an antitumor drug in the future.
肺癌是最常被诊断出的恶性肿瘤,并且是全球发病和死亡的主要原因之一。地塞米松(DEX)在调节肺癌细胞增殖中发挥重要作用;然而,其中涉及的机制仍然未知。在本研究中,检测了DEX对A549细胞增殖和凋亡的影响,以及这些影响潜在的下游调控机制。在12、24和48小时时间点用不同浓度的DEX处理A549细胞,随后添加SB431542(一种TGF-β1受体抑制剂)以阻断TGF-β1信号通路。使用3-(4,5-二乙基噻唑-2-基)-5-(3-羧甲氧基苯基)-2-(4-磺基苯基)-2H-四唑鎓内盐分析细胞增殖。通过Hoechst 33342和膜联蛋白V/碘化丙啶染色测量凋亡率,并通过蛋白质印迹法评估转化生长因子(TGF)-β1、Smad家族成员2(Smad2)和半胱天冬酶-3的表达。本研究结果表明,DEX处理后A549细胞的增殖减少且凋亡率显著增加(P<0.05)。此外,DEX刺激后TGF-β1、Smad2和半胱天冬酶-3的表达显著增加(P<0.05),添加TGF-β1受体抑制剂SB431542可消除这些影响(P<0.05)。DEX诱导A549细胞凋亡,并且这种作用被TGF-β1受体信号抑制剂SB431542消除,这表明TGF-β1/Smad2通路可能与该过程相关,并且SB431542未来可能作为一种抗肿瘤药物发挥作用。