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Apoptosis prediction via inhibition of AKT signaling pathway by neogrifolin

机译:通过抑制新葛根素抑制AKT信号通路来预测细胞凋亡

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摘要

Neogrifolin, a natural biologically active substance isolated from the edible bodies of the mushroom Albatrellus confluens, has been shown to possess several pharmacological properties. No studies were investigated against osteosarcoma cancer. Hence, in this study, we investigated the apoptosis-inducing effects and the mechanisms of neogrifolin on human osteosarcoma cells. Our results demonstrated that neogrifolin induced concentration- and time-dependent suppression of proliferation. Further, induction of apoptosis in U2OS and MG63 osteosarcoma cell lines were also observed. Neogrifolin induced the release of cytochrome c accompanied by activation of caspase-9, caspase-3 and cleavage of poly (ADP-ribose) polymerase (PARP). In addition, z-VAD-fmk, a universal inhibitor of caspases, prevented caspase-3 activation and PARP cleavage and inhibited neogrifolin-induced cell growth inhibition. Furthermore, neogrifolin treatment resulted in a reduction of phosphorylated AKT level, FOXO transcription factor, and glycogen synthase kinase 3 (GSK3). Knockdown of GSK3 with siRNA inhibited the apoptotic effects of neogrifolin. On the other hand, neogrifolin treatment also down-regulated the expression of the inhibitor of apoptosis protein (IAP) in both osteosarcoma cells. Collectively, our results suggested that neogrifolin is a potential candidate for osteosarcoma.
机译:Neogrifolin是一种天然的生物活性物质,它是从蘑菇菇中的食用菌中分离出来的,具有多种药理特性。没有研究针对骨肉瘤癌症的研究。因此,在这项研究中,我们研究了凋亡的诱导作用和新草蔻素对人骨肉瘤细胞的作用机制。我们的研究结果表明,新骨灰素诱导浓度和时间依赖性抑制增殖。此外,还观察到了U2OS和MG63骨肉瘤细胞系中凋亡的诱导。 Neogrifolin诱导细胞色素c的释放,同时激活caspase-9,caspase-3并切割聚(ADP-核糖)聚合酶(PARP)。此外,半胱天冬酶的通用抑制剂z-VAD-fmk可以阻止caspase-3激活和PARP裂解,并抑制新农杆菌素诱导的细胞生长抑制。此外,新grifolin治疗导致磷酸化的AKT水平,FOXO转录因子和糖原合酶激酶3(GSK3)降低。用siRNA敲低GSK3抑制了新农夫林的凋亡作用。另一方面,新骨灰素治疗还下调了两个骨肉瘤细胞中凋亡蛋白抑制剂(IAP)的表达。总的来说,我们的结果表明,新骨灰素是骨肉瘤的潜在候选者。

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