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首页> 外文期刊>Nutrition and Cancer: An International Journal >Ethanolic Extract of Lagerstroemia Speciosa (L.) Pers., Induces Apoptosis and Cell Cycle Arrest in HepG2 Cells
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Ethanolic Extract of Lagerstroemia Speciosa (L.) Pers., Induces Apoptosis and Cell Cycle Arrest in HepG2 Cells

机译:Lagerstroemia Speciosa(L.)的乙醇提取物。,诱导HepG2细胞中的细胞凋亡和细胞周期骤停

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Lagerstroemia speciosa (L.) Pers., (Lythraceae) also called Banaba is a native plant of southeast Asia and is widely used in traditional medicinal system. Herbal tea from banaba leaves are used to reduce weight and diabetes. We investigated the cytotoxic potentials of ethanolic banaba leaves extract (EBLE) against human hepatocellular carcinoma (HepG2) cell line. Lagerstroemia speciosa leaves were extracted and obtained from M/s. Quimico Herbal Extract Manufacturer, Bengaluru, India, and it contains 20% corosolic acid. Cells were treated with 50, 100, and 150 mu g/ml of EBLE for 24 h, and cytotoxicity was evaluated by MTT assay. Apoptosis-related morphology was investigated by DAPI nuclear staining. Protein and gene expressions of p-Akt, FOXO1, p53, MDM2, p21, p27, CDK4, cyclin D1, and E1 were evaluated through Western blotting and qPCR. EBLE treatments caused significant, concentration-dependent cytotoxicity. DAPI staining and flow cytometry studies showed chromatin condensation, increased apoptotic cell population and cell cycle arrest at subG0/G1 phase upon EBLE treatments respectively. Furthermore, EBLE treatments significantly increased the expressions of p53, p21, p27, FOXO1, while p-Akt, MDM2, CDK4, cyclin D1, and E1 expressions were downregulated. These findings suggested that EBLE induces G1-phase of cell cycle arrest and apoptosis in HepG2 cells. EBLE may serve as a therapeutic agent against hepatocellular carcinoma.
机译:Lagerstroemia Speciosa(L.)Pers。(Lytheraceae)也叫做Banaba是东南亚的原生植物,广泛用于传统药物系统。来自Banaba叶子的清凉茶用于减轻重量和糖尿病。我们研究了乙醇甘露肠叶(EBEL)对人肝细胞癌(HepG2)细胞系的细胞毒性潜力。 Lagerstroemia Speciosa叶被提取并从M / s获得。 Quimico Herbal提取制造商,班加罗鲁,印度,它含有20%的凝胶酸。将细胞用50,100和150μg/ ml的EBBER处理24小时,并通过MTT测定评估细胞毒性。 DAPI核染色研究了凋亡相关的形态学。通过蛋白质印迹和QPCR评估P-AKT,FOXO1,P53,MDM2,P21,P27,CDK4,Cyclin D1和E1的蛋白质和基因表达。 EBLE治疗导致显着,浓度依赖性细胞毒性。 DAPI染色和流式细胞术研究分别显示染色质缩合,分别在EBE0 / G1相时增加了凋亡细胞群和细胞周期停滞。此外,EBEL处理显着增加了P53,P21,P27,FOXO1的表达,而P-AKT,MDM2,CDK4,细胞周期蛋白D1和E1表达式被下调。这些发现表明,EBEL在HepG2细胞中诱导细胞周期停滞和细胞凋亡的G1相。 EBEL可以作为针对肝细胞癌的治疗剂。

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