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Effects of karanjin on cell cycle arrest and apoptosis in human A549, HepG2 and HL-60 cancer cells

机译:卡兰金对人A549,HepG2和HL-60癌细胞的细胞周期阻滞和凋亡的影响

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We have investigated the potential anticancer effects of karanjin, a principal furanoflavonol constituent of the Chinese medicine Fordia cauliflora, using cytotoxic assay, cell cycle arrest, and induction of apoptosis in three human cancer cell lines (A549, HepG2 and HL-60 cells). MTT cytotoxic assay showed that karanjin could inhibit the proliferation and viability of all three cancer cells. The induction of cell cycle arrest was observed via a PI (propidium iodide)/RNase Staining Buffer detection kit and analyzed by flow cytometry: karanjin could dose-dependently induce cell cycle arrest at G2/M phase in the three cell lines. Cell apoptosis was assessed by Annexin V-FITC/PI staining: all three cancer cells treated with karanjin exhibited significantly increased apoptotic rates, especially in the percentage of late apoptosis cells. Karanjin can induce cancer cell death through cell cycle arrest and enhance apoptosis. This compound may be effective clinically for cancer pharmacotherapy.
机译:我们使用细胞毒性测定,细胞周期阻滞和诱导三种人类癌细胞系(A549,HepG2和HL-60细胞)的细胞毒性试验研究了卡兰金(呋喃黄酮的主要成分)的潜在抗癌作用。 MTT细胞毒性试验表明,卡那金可以抑制所有三种癌细胞的增殖和活力。通过PI(碘化丙啶)/ RNase染色缓冲液检测试剂盒观察到了细胞周期停滞的诱导,并通过流式细胞术进行了分析:karanjin可以剂量依赖性地诱导三种细胞系中G2 / M期的细胞周期停滞。通过膜联蛋白V-FITC / PI染色评估细胞凋亡:用karanjin处理的所有三种癌细胞均显示出显着增加的凋亡率,尤其是晚期凋亡细胞的百分比。 Karanjin可通过细胞周期停滞诱导癌细胞死亡并增强细胞凋亡。该化合物在临床上可能对癌症药物治疗有效。

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