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Induction of apoptosis in tumor cells by Licorice root flavonoids in vitro

机译:甘草根黄酮在体外诱导肿瘤细胞凋亡

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Previously, we have shown that an experimental sample of licorice root flavonoids (LRF), inhibits proliferation of tumor cells in a dose dependent manner. The aim of this study was to evaluate the ability of LRF to induce apoptosis as a possible mechanism for its antiproliferative effect. The study was done by flow cytometry (Cytomics FC 500 Beckman Coulter, USA) and performed using a DNA-specific fluorochrome propidium iodide (Sigma, USA). The ability of LRF to induce apoptosis was studied against histologically different cell lines (U-937, A-431, GL-6). After 24 h of incubation of tumor cell lines with LRF (20 mkg/ml) there was a slight increase of apoptosis level for 10-15%. By 48 h incubation there were observed a statistically significant increase in the levels of apoptotic and tetraploid cells. Therefore we can conclude the following: evidently inhibition of proliferation of tumor cells is the result of G2/M cell cycle arrest, which causes their eventual apoptosis.
机译:以前,我们已经表明,甘草根黄酮(LRF)的实验样品以剂量依赖性方式抑制肿瘤细胞的增殖。 本研究的目的是评估LRF作为其抗增殖效应的可能机制诱导细胞凋亡的能力。 该研究通过流式细胞术(细胞素FC 500 Beckman Coulter,USA)进行,并使用DNA特异性荧光染料碘化物(Sigma,USA)进行。 对组织学不同的细胞系(U-937,A-431,GL-6)研究了LRF诱导细胞凋亡的能力。 24小时后用LRF(20mKg / ml)孵育肿瘤细胞系后,凋亡水平略微增加10-15%。 孵育48小时,观察到凋亡和四倍体细胞水平的统计学显着增加。 因此,我们可以得出结论:显然对肿瘤细胞增殖的抑制是G2 / M细胞循环骤停的结果,这导致其最终凋亡。

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