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Anticancer activity of okra raw polysaccharides extracts against human liver cancer cells

机译:黄秋葵粗多糖提取物对人肝癌细胞的抗癌活性

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Purpose: To examine raw polysaccharides extract of okra (Abelmoschus esculentus L.) as an anticancer agent against human liver cancer cells. Methods: Okra raw polysaccharide extract (ORPE) was obtained by ethanol extraction from the raw fruit. Huh7it cells were grown in DMEM (Dulbecco's Modified Eagle Medium) and cultured for 24 h prior to treatment with the extract. The cell culture was divided into 3 groups, viz, negative control group (KN), positive control group (KP, treated with 10 μg/mL doxorubicin), and ORPE (P) group. ORPE group was divided into 5 subgroups based on the dose used for treatment, viz, 50 (P1), 100 (P2), 200 (P3), 400 (P4), and 600 μg/mL (P5). Huh7it cell proliferation was measured by MTT assay. while measurement of Huh7it cell apoptosis, necrosis, and cell cycle analysis were carried out using Annexin V FITC-PI antibody test and flow cytometry. Results: ORPE significantly inhibited Huh7it cell proliferation and induced apoptosis. ORPE treatment with 600 μg/mL extract caused 5.82 % late cell apoptosis and 5.62 % early apoptosis. Cell cycle arrest occurred during G0/G1 phase. Conclusion: ORPE is a potential anticancer agent against human liver cancer cells due to its ability to induce apoptosis of huh7it cells by promoting cell cycle arrest during G0/G1 phase.
机译:目的:研究秋葵的粗多糖提取物(Abelmoschus esculentus L.)作为抗人肝癌细胞的抗癌剂。方法:采用乙醇提取法从生果中提取黄秋葵粗多糖提取物(ORPE)。 Huh7it细胞在DMEM(Dulbecco改良的Eagle培养基)中生长,并培养24小时,然后用提取物处理。将细胞培养物分为3组,即阴性对照组(KN),阳性对照组(KP,用10μg/ mL阿霉素处理)和ORPE(P)组。根据治疗剂量,ORPE组分为5个亚组,即50(P1),100(P2),200(P3),400(P4)和600μg/ mL(P5)。通过MTT测定法测量Huh7it细胞增殖。同时使用Annexin V FITC-PI抗体测试和流式细胞仪进行Huh7it细胞凋亡,坏死和细胞周期分析的测量。结果:ORPE显着抑制Huh7it细胞增殖并诱导凋亡。用600μg/ mL提取物进行ORPE处理可导致5.82%的晚期细胞凋亡和5.62%的早期凋亡。细胞周期停滞发生在G0 / G1期。结论:ORPE通过在G0 / G1期促进细胞周期阻滞而诱导huh7it细胞凋亡,具有潜在的抗人肝癌细胞的作用。

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