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Puerarin induces cell apoptosis in human chondrosarcoma cell line SW1353 via inhibition of the PI3K/Akt signaling pathway

机译:葛根素通过抑制PI3K / Akt信号通路诱导人软骨肉瘤细胞SW1353细胞凋亡

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摘要

Chondrosarcoma is a malignant soft tissue sarcoma with poor prognosis. Puerarin has been demonstrated to possess anticancer properties; however, the effects of puerarin in human chondrosarcoma cells remain unknown. The present study aimed to investigate the anticancer effects of puerarin in SW1353 human chondrosarcoma cells. SW1353 cells were treated with increasing concentrations of puerarin for different durations. Cell viability was evaluated using MTT assays. Cell apoptosis rates were determined by flow cytometry. The activities of caspase-3 and caspase-9 were measured by enzymatic assay. The expression of RAC-alpha serine/threonine-protein kinase (Akt), phosphorylated-Akt, caspase-3 and apoptosis-associated proteins, including B-cell lymphoma 2 (Bcl-2) and Bcl-2-associated X protein (Bax) were detected by western blotting. Puerarin significantly decreased cell viability and significantly induced apoptosis of SW1353 cells. In addition, puerarin significantly increased the enzymatic activities of caspase-3 and caspase-9. Puerarin treatment suppressed the expression of p-Akt and Bcl-2 but promoted the expression of Bax and cleaved caspase-3 in SW1353 cells. Notably, the phosphatidylinositol 3-kinase (PI3K) inhibitor abrogated the decreased phosphorylation of Akt, suggesting that the PI3K/Akt signaling pathway is involved in mediating the anticancer effects of puerarin. The data from the present study indicated that puerarin exhibits anticancer effects in SW1353 cells and may be a potential therapeutic drug for patients with chondrosarcoma.
机译:软骨肉瘤是一种恶性软组织肉瘤,预后较差。葛根素已被证明具有抗癌特性。然而,葛根素在人软骨肉瘤细胞中的作用仍然未知。本研究旨在研究葛根素对SW1353人软骨肉瘤细胞的抗癌作用。用不同浓度的葛根素处理SW1353细胞不同的持续时间。使用MTT测定法评估细胞活力。细胞凋亡率通过流式细胞术确定。通过酶法测定caspase-3和caspase-9的活性。 RAC-α丝氨酸/苏氨酸蛋白激酶(Akt),磷酸化Akt,caspase-3和凋亡相关蛋白的表达,包括B细胞淋巴瘤2(Bcl-2)和Bcl-2相关X蛋白(Bax )通过蛋白质印迹检测。葛根素显着降低细胞生存力并显着诱导SW1353细胞凋亡。此外,葛根素显着提高了caspase-3和caspase-9的酶活性。葛根素处理抑制了SW1353细胞中p-Akt和Bcl-2的表达,但促进了Bax的表达和caspase-3的裂解。值得注意的是,磷脂酰肌醇3激酶(PI3K)抑制剂消除了Akt磷酸化的降低,这表明PI3K / Akt信号传导途径参与了葛根素的抗癌作用。来自本研究的数据表明,葛根素在SW1353细胞中具有抗癌作用,并且可能是软骨肉瘤患者的潜在治疗药物。

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