首页> 外文期刊>International journal of molecular medicine >Thermosensitization and induction of apoptosis or cell-cycle arrest via the MAPK cascade by parthenolide, an NF-kappaB inhibitor, in human prostate cancer androgen-independent cell lines.
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Thermosensitization and induction of apoptosis or cell-cycle arrest via the MAPK cascade by parthenolide, an NF-kappaB inhibitor, in human prostate cancer androgen-independent cell lines.

机译:在人类前列腺癌雄激素非依赖性细胞系中,通过单酚(一种NF-κB抑制剂)通过MAPK级联进行热敏化和诱导凋亡或细胞周期停滞。

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摘要

Parthenolide (PTL), a nuclear factor-kappaB (NF-kappaB) inhibitor, has a significant thermo-enhancement effect. Modification of thermosensitivity by treatment with PTL prior to hyperthermia was investigated in the human prostate cancer androgen-independent cell lines PC3 and DU145. In addition, we analyzed the mechanisms related to induction of apoptosis or G/M cell-cycle arrest via the effects of ERK1/2, p38 and SAPK/JNK signaling on mitogen-activated protein kinase (MAPK). Lethal damage caused by mild hyperthermia at 41.0 C or 42.0 C in both cell lines resulted in a low level of thermosensitivity, while sequential combination with PTL showed significant thermosensitization. Step-up hyperthermia (SUH) (42 C for 30 min, 43.0 C or 43.5 C for various periods) reduced the thermosensitivity of the cells to second heating. However, PTL given as pre-treatment prior to SUH prevented SUH-induced thermal tolerance and resulted in significant thermosensitization. Induction of apoptosis by the combination of PTL and hyperthermia at 44.0 C was determined by the ratio of sub-G1 division cells using flow cytometry, which was increased significantly in comparison with single treatment, and was more effective in PC3 than DU145 cells. The behavior of ERK1/2, p38, and SAPK/JNK signaling in the MAPK cascade by treatment with PTL and hyperthermia were examined by Western blotting. As for PC3 cells, ras-downstream p-ERK1/2 was activated and p-p38 slightly activated by combined treatment with PTL and hyperthermia in comparison with each alone. As for DU145 cells, ERK1/2 was not changed, while p38 and SAPK/JNK were slightly activated by combination treatment. These results were related to increases in the induction of apoptosis, G/M cell cycle arrest, and lethal damage of cells via the MAPK cascade. Together, our findings demonstrate that PTL is an effective thermosensitizing agent for multidisciplinary therapy for human prostate cancer.
机译:Parthenolide(PTL)是一种核因子-κB(NF-kappaB)抑制剂,具有显着的热增强作用。在人类前列腺癌雄激素非依赖性细胞系PC3和DU145中,研究了在热疗之前通过PTL处理热敏感性的改变。此外,我们通过对有丝分裂原激活的蛋白激酶(MAPK)的ERK1 / 2,p38和SAPK / JNK信号传导的作用,分析了与诱导凋亡或G / M细胞周期停滞有关的机制。两种细胞系在41.0 C或42.0 C时由温和的高温引起的致死性损害导致较低的热敏性水平,而与PTL的顺序组合显示出显着的热敏性。逐步升温(SUH)(42°C持续30分钟,43.0 C或43.5 C持续不同的时间)降低了细胞对第二次加热的热敏性。但是,在SUH之前进行预处理的PTL阻止了SUH引起的热耐受性并导致显着的热敏性。通过使用流式细胞术通过亚G1分裂细胞的比例确定在44.0 C时PTL和热疗的组合诱导的凋亡,与单次治疗相比显着增加,并且在PC3中比DU145细胞更有效。通过蛋白质印迹和热疗检查了MAPK级联中ERK1 / 2,p38和SAPK / JNK信号在MAPK级联反应中的行为。对于PC3细胞,与单独使用PTL和高温治疗相结合,ras下游p-ERK1 / 2被激活,p-p38被轻微激活。至于DU145细胞,ERK1 / 2没有改变,而p38和SAPK / JNK通过联合处理被轻微激活。这些结果与细胞凋亡的诱导增加,G / M细胞周期停滞以及经由MAPK级联的细胞致死性损伤有关。总之,我们的发现表明PTL是用于人类前列腺癌的多学科治疗的有效热敏剂。

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