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Allyl isothiocyanate triggers G2/M phase arrest and apoptosis in human brain malignant glioma GBM 8401 cells through a mitochondria-dependent pathway

机译:allyl isothiocyanate triggers G2/m phase arrest and apoptosis in human brain malignant glioma GBm 8401 cells through a mitochondria-dependent pathway

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摘要

Isothiocyanates (ITCs) are present as glucosinolates in various cruciferous vegetables. Allyl isothiocyanate (AITC) is one of the common naturally occurring isothiocyanates. Recent studies have shown that AITC significantly inhibited survival of leukemia HL-60, bladder cancer UM-UC-3 and colon cancer HT-29 cells in vitro. In this study, we demonstrate that AITC significantly decreased proliferation and viability of human brain malignant glioma GBM 8401 cells in a dose-dependent manner with IC(50) 9.25+/-0.69 mu M for 24 h-treatment. The analysis of cell cycle distribution also showed that AITC induced significantly G2/M arrest and sub-G1 phase (apoptotic population) in GBM 8401 cells. AITC markedly reduced the CDK1/cyclin B activity and protein levels by CDK1 activity assay and Western blot analysis. AITC-induced apoptotic cell death and this evidence was confirmed by morphological assessment and DAPI staining. Pretreatment with specific inhibitors of caspase-3 (Z-DEVE-FMK) and -9 (Z-LEHD-FMK) significantly reduced caspase-3 and -9 activity in GBM 8401 cells. Western blot analysis and colorimetric assays also displayed that AITC caused a time-dependent increase in cytosolic cytochrome c, pro-caspase-9, Apaf-1, AIF, Endo G and the stimulated caspase-9 and -3 activity. Our results suggest that AITC is a potent anti-human brain malignant glioma drug and it shows a remarkable action on cell cycle arrest before commitment for apoptosis is reached.
机译:异硫氰酸酯(ITC)以硫代葡萄糖苷的形式存在于各种十字花科蔬菜中。异硫氰酸烯丙酯(AITC)是常见的天然异硫氰酸酯之一。最近的研究表明,AITC在体外显着抑制白血病HL-60,膀胱癌UM-UC-3和结肠癌HT-29细胞的存活。在这项研究中,我们证明AITC以剂量依赖性方式显着降低人脑恶性神经胶质瘤GBM 8401细胞的增殖和活力,IC(50)为9.25 +/- 0.69μM,持续24小时治疗。对细胞周期分布的分析还表明,AITC在GBM 8401细胞中诱导了显着的G2 / M停滞和亚G1期(凋亡群体)。通过CDK1活性测定和Western blot分析,AITC显着降低了CDK1 / cyclin B活性和蛋白质水平。 AITC诱导的凋亡细胞死亡,这一证据通过形态学评估和DAPI染色得到了证实。用caspase-3(Z-DEVE-FMK)和-9(Z-LEHD-FMK)的特异性抑制剂进行预处理可以显着降低GBM 8401细胞中的caspase-3和-9活性。 Western印迹分析和比色分析还显示,AITC引起了细胞溶质中的细胞色素c,半胱天冬酶原9,Apaf-1,AIF,Endo G和刺激的半胱天冬酶9和-3活性的时间依赖性增加。我们的结果表明,AITC是一种有效的抗人脑恶性神经胶质瘤药物,在达到凋亡承诺之前,它对细胞周期停滞表现出显着作用。

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