Zhejiang Medical College, Hangzhou, 310053, China.
J Cancer Res Clin Oncol. 2012 Jan;138(1):119-24. doi: 10.1007/s00432-011-1080-3. Epub 2011 Nov 3.
Non-steroidal anti-inflammatory drugs (NSAIDs) can induce the apoptosis of many tumor cells and inhibit their growth. NS398 is an NSAID that inhibits COX-2 expression and induces tumor apoptosis via other pathways. The current study aims to observe the effects of NS398 on A549 cell apoptosis and investigate the apoptosis mechanism.
The A549 cells were treated with different NS398 concentrations. The growth inhibition of A549 cell was analyzed via a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, and morphologic alterations were observed to detect apoptosis. The expression of survivin and caspase-3 mRNA was quantified via reverse transcriptase polymerase chain reaction, and the expression of caspase-3 and p-AKT protein was detected via western blot analysis.
The MTT results show that NS398 inhibits A549 cell growth. The inhibition rate of NS398 (400 μmol/L) on A549 cells is up to 66.95% after 48 h of treatment. Simultaneously, the morphology experiment revealed significant apoptotic characteristics in A549 cells, such as green nuclear plasmid and different degrees of nuclear fragmentation. The expression of survivin mRNA was significantly reduced (P < 0.05, P < 0.01, and P < 0.001) and that of caspase-3 mRNA was significantly increased (P < 0.05 and P < 0.001) in the group treated with NS398 for 24 h in a dose-dependent manner. On the other hand, survivin and p-AKT were expressed at low levels (P < 0.01 and P < 0.001) and caspase-3 was increased significantly (P < 0.05 and P < 0.001) in the group treated with NS398 for 48 h in a dose-dependent manner.
The current study proves that NS398 induces apoptosis in A549 cells, thereby inhibiting tumor growth. This function of NS398 may be related to the inhibition of AKT phosphorylation and survivin protein downregulation.
非甾体抗炎药(NSAIDs)可诱导多种肿瘤细胞凋亡并抑制其生长。NS398 是一种抑制 COX-2 表达并通过其他途径诱导肿瘤细胞凋亡的 NSAID。本研究旨在观察 NS398 对 A549 细胞凋亡的影响,并探讨其凋亡机制。
用不同浓度 NS398 处理 A549 细胞。用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法分析 A549 细胞生长抑制情况,观察形态学改变以检测细胞凋亡。用逆转录聚合酶链反应定量检测存活素和半胱天冬酶-3mRNA 的表达,用 Western blot 分析检测半胱天冬酶-3 和磷酸化 AKT 蛋白的表达。
MTT 结果显示 NS398 抑制 A549 细胞生长。NS398(400μmol/L)处理 A549 细胞 48 h 后抑制率可达 66.95%。同时,形态学实验显示 A549 细胞出现明显的凋亡特征,如绿色核质体和不同程度的核碎裂。NS398 处理 24 h 时,存活素 mRNA 的表达明显降低(P<0.05,P<0.01 和 P<0.001),半胱天冬酶-3 mRNA 的表达明显升高(P<0.05 和 P<0.001),且呈剂量依赖性;NS398 处理 48 h 时,存活素和磷酸化 AKT 表达水平降低(P<0.01 和 P<0.001),半胱天冬酶-3 表达升高(P<0.05 和 P<0.001),且呈剂量依赖性。
本研究证明 NS398 诱导 A549 细胞凋亡,从而抑制肿瘤生长。NS398 的这种功能可能与抑制 AKT 磷酸化和下调存活素蛋白有关。