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In vitro evaluation of Annona muricata L. (Soursop) leaf methanol extracts on inhibition of tumorigenicity and metastasis of breast cancer cells

机译:Annona Muricata L.(Soursop)叶甲醇提取物的体外评价抑制肿瘤癌细胞的抑制作用和转移

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PurposeThe present study evaluates the in-vitro anti-tumorigenic potential of leaf methanol extracts of Annona muricata (LMAM).Materials and methodsThe cytotoxic activity was assessed in MCF-7 cells by MTT assay at various concentrations ranging from 25-250 mu g/mL. MCF-7 cells were treated with 50 and 100 mu g/mL LMAM for 24 h. To detect LMAM-induced apoptosis; Hoescht 33342 staining along with Cell cycle analysis, Annexin-PI probe as well as oxidative stress damage by reactive oxygen species (ROS) measurements were determined using flow cytometric analysis. While caspase-3 expression levels were studied employing the qRT-PCR method.ResultsLMAM exhibited significant inhibition of MCF-7 cells with an IC50 value of 85.55 mu g/mL. Hoescht staining showed marked morphological features characteristic of apoptosis in LMAM treated cells. Cell cycle analysis confirmed the proven capability of LMAM showing a 30% rise in G(1) phase upon treatment with 100 mu g/mL LMAM, thus inducing cell cycle arrest at G(1) phase and a rise in sub G(0)-G(1) population paralleled with a decrease in S phase. Flow cytometric analysis with Annexin V-FITC-PI staining indicated an increase in the early and late apoptotic population with a 3.38% and 19.47% rise respectively when treated with 100 mu g/mL LMAM. Treatment with 100 mu g/mL LMAM caused an increase in intracellular ROS with MFI value 3334.08. Upregulation of caspase-3 was observed with a 2.18 and 32.47 fold increase compared to control in MCF-7 cells cultured at 50 mu g/mL and 100 mu g/mL LMAM respectively suggesting caspase-dependent apoptosis.ConclusionLMAM proved as a potent ethno-chemopreventive agent and a potential lead in cancer treatment attributable to the synergistic interactive properties of phytoconstituents.
机译:目的研究评估了Annona Muricata(LMAM)的叶片甲醇提取物的体外抗致致旋转致致致致致致致旋转潜力。在MCF-7细胞中,通过MTT测定以25-250μmg/ ml的各种浓度评估细胞毒性活性的细胞毒性活性。 。用50-100μg/ mm LMAM处理MCF-7细胞24小时。检测LMAM诱导的细胞凋亡;使用流式细胞术分析确定Hoescht 33342染色和通过反应性氧物质(ROS)测量的氧化应激损伤以及氧化应激损伤。在使用QRT-PCR方法中研究了Caspase-3表达水平。方法表现出显着抑制MCF-7细胞,IC50值为85.55μg/ mL。 Hoescht染色显示出LMAM处理细胞中凋亡的明显形态特征。细胞循环分析证实了LMAM在用100μg/ mL LMAM处理后显示出G(1)相的30%升高的证明能力,从而在G(1)相时诱导细胞周期滞留和子G(0)的上升-G(1)平行于S相的降低的人口。流式细胞术分析与附膜蛋白V-FITC-PI染色表明,在用100μg/ ml LMAM处理时,分别增加了3.38%和19.47%的增加3.38%和19.47%。用100μg/ mm的处理引起MFI值3334.08的细胞内RO增加。在分别暗示Caspase依赖性凋亡的MCF-7细胞中,在2.18和32.47倍增加中,观察到Caspase-3的上调,以2.18和32.47倍增加。组织依赖性凋亡的MCF-7细胞。Clusionmam被证明是有效的民族化学预防剂和癌症治疗的潜在铅,可归因于植物植物植物的协同互动性质。

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