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Inhibition of NF-κB by combination therapy with parthenolide and hyperthermia and kinetics of apoptosis induction and cell cycle arrest in human lung adenocarcinoma cells

机译:孤雌酚和热疗联合治疗对NF-κB的抑制及其诱导人肺腺癌细胞凋亡的动力学和细胞周期阻滞。

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We investigated the mechanisms of thermosensitization related to combination therapy with sesquiterpene lactone parthenolide (PTL), a nuclear factor-κB (NF-κB) inhibitor, and hyperthermia using human lung adenocarcinoma cells A549. The kinetics of apoptosis induction and cell cycle of cells treated with PTL, heating, and combined treatment were examined by flow cytometric analysis. The flow cytometric distribution was calculated and expressed as a percentage. The ratios of the sub-G1 division, used to determine the induction of apoptosis, increased significantly with the combination therapy. Furthermore, the ratios of G2/M division increased and the ratios of G0/G1 division decreased, indicating cell cycle arrest in G2/M. The cell phase response to PTL by A549 cells synchronized in the G1/S border with hydroxyurea was also analyzed. PTL showed remarkable cytotoxicity at the S phase of the cell cycle in A549 cells at all concentrations as well as with hyperthermia, thus PTL reduced the number of cells in the proliferation phase. Inhibition of intracellular transcription factor NF-κB activation in A549 cells with various incubation periods after treatments with PTL, heating and combined treatment was examined by Western blot analysis. Unexpectedly, PTL alone did not inhibit NF-κB activation in cells stimulated with TNF-α, while heating alone inhibited NF-κB early after treatment and that effect faded over time. In contrast, PTL combined with heating completely inhibited NF-κB activation. Our results demonstrated that PTL and heating in combination cause significant thermosensitization of A549 cells via induction of apoptosis or cell cycle arrest in G2/M by inhibiting NF-κB activation in a synergistic manner.
机译:我们研究了与倍半萜内酯单酚(PTL),核因子-κB(NF-κB)抑制剂和热疗联合使用人肺腺癌细胞A549的热敏化机制。流式细胞术分析了PTL,加热和联合处理后的细胞凋亡诱导动力学和细胞周期。计算流式细胞仪分布并将其表示为百分比。用于确定细胞凋亡诱导作用的sub-G1分区的比率随着联合疗法的增加而显着增加。此外,G2 / M分裂的比率增加而G0 / G1分裂的比率减少,表明G2 / M中的细胞周期停滞。还分析了在G1 / S边界与羟基脲同步的A549细胞对PTL的细胞相反应。在所有浓度以及热疗作用下,PTL在A549细胞的细胞周期S期均表现出显着的细胞毒性,因此PTL减少了增殖期的细胞数量。用PTL处理,加热和联合处理后,在不同的潜伏期对A549细胞中胞内转录因子NF-κB的抑制作用进行了Western blot分析。出乎意料的是,单独的PTL不会抑制TNF-α刺激的细胞中NF-κB的活化,而单独加热会在治疗后早期抑制NF-κB,并且这种作用会随着时间而逐渐消失。相反,PTL结合加热完全抑制了NF-κB的活化。我们的结果表明,PTL和加热相结合可通过诱导细胞凋亡或通过协同抑制NF-κB活化来抑制G2 / M中的细胞周期而引起A549细胞显着的热敏化。

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