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首页> 外文期刊>Journal of cellular and molecular medicine. >A biflavonoid‐rich extract from Selaginella moellendorffii Hieron. induces apoptosis via STAT3 and Akt/NF‐κB signalling pathways in laryngeal carcinoma
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A biflavonoid‐rich extract from Selaginella moellendorffii Hieron. induces apoptosis via STAT3 and Akt/NF‐κB signalling pathways in laryngeal carcinoma

机译:来自SelAginella Moellendorffii Hieron的双链脂肪醛提取物。喉部癌中的STAT3和AKT / NF-κB信号传导途径诱导细胞凋亡

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摘要

Selaginella moellendorffii Hieron. (SM), a perennial evergreen plant, has been used in the treatment of acute infectious hepatitis, thoracic and hypochondriac lumbar contusions, systemic oedema and thrombocytopaenia. However, the role of a biflavonoid-rich extract from SM (SM-BFRE) in anti-larynx cancer has rarely been reported. In this study, the in vitro and in vivo anti-laryngeal cancer activity and potential mechanisms of SM-BFRE were investigated. An off-line semipreparative liquid chromatography-nuclear magnetic resonance protocol was carried out to determine six biflavonoids from SM-BFRE. In vitro, MTT assay revealed that SM-BFRE inhibited the proliferation of laryngeal carcinoma cells. A wound healing assay indicated that SM-BFRE suppressed the migration of laryngeal cancer cells. Hoechst 33?258 and Annexin V-FITC/PI double staining assays were performed and verified that SM-BFRE induced apoptosis in laryngeal carcinoma cells. The Hep-2 bearing nude mouse model confirmed that SM-BFRE also exhibited anticancer effect in vivo. In addition, Western blot analysis demonstrated that SM-BFRE exerted its anti-laryngeal cancer effect by activating the mitochondrial apoptotic pathway and inhibiting STAT3 and Akt/NF-κB signalling pathways. All results suggested that SM-BFRE could be considered as a potential chemotherapeutic drug for laryngeal cancer.? 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.
机译:Selaginella Moellendorffii Hieron。 (SM)是一只多年生常绿植物,已用于治疗急性传染性肝炎,胸椎和次闭腰椎血清缺血,全身水肿和血小板减少症。然而,富含双歧脂素的提取物来自SM(SM-BFRE)在抗喉癌​​中的作用很少已经报道。在本研究中,研究了体外和体内抗喉癌癌症活性以及SM-BFRE的潜在机制。进行了离线半分法液相色谱 - 核磁共振方案以确定来自SM-BFRE的六个双链糖。体外,MTT测定显示SM-BFRE抑制喉癌细胞的增殖。伤口愈合测定表明,SM-BFRE抑制了喉癌细胞的迁移。 HOECHST 33?258和膜蛋白V-FITC / PI双染色测定进行,并验证了SM-BFRE诱导喉癌细胞的细胞凋亡。 HEP-2轴承裸鼠模型证实SM-BFRE在体内也表现出抗癌效果。此外,Western印迹分析证明SM-BFRE通过激活线粒体凋亡途径和抑制STAT3和AKT / NF-κB信号传导途径来施加其抗喉癌癌症。所有结果表明,SM-BFRE可以被认为是喉癌的潜在化学治疗药物。? 2020作者。细胞和分子医学基础和约翰瓦里&SONS&LTD的蜂窝和分子医学杂志。

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