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Triterpenoid saponin flaccidoside II from Anemone flaccida triggers apoptosis of NF1-associated malignant peripheral nerve sheath tumors via the MAPK-HO-1 pathway

机译:海葵黄酮中的三萜皂苷类黄酮糖苷II通过MAPK-HO-1途径触发与NF1相关的恶性周围神经鞘瘤的凋亡

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Malignant peripheral nerve sheath tumors (MPNSTs) are highly aggressive soft tissue neoplasms that are extremely rare and are frequently associated with neurofibromatosis type 1 patients. MPNSTs are typically fatal, and there is no effective treatment so far. In our previous study, we showed that flaccidoside II, one of the triterpenoid saponins isolated from Anemone flaccida Fr. Schmidt, has antitumor potential by inducing apoptosis. In the present study, we found that flaccidoside II inhibits proliferation and facilitates apoptosis in MPNST cell lines ST88-14 and S462. Furthermore, this study provides a mechanism by which the downregulation of heme oxygenase-1 via extracellular signal-regulated kinase-1/2 and p38 mitogen-activated protein kinase pathways is involved in the apoptotic role of flaccidoside II. This study suggested the potential of flaccidoside II as a novel pharmacotherapeutic approach for MPNSTs.
机译:恶性周围神经鞘瘤(MPNSTs)是高度侵袭性的软组织肿瘤,极为罕见,经常与1型神经纤维瘤病患者相关。 MPNST通常是致命的,到目前为止还没有有效的治疗方法。在我们之前的研究中,我们显示了黄柏苷II,一种从银莲花Fr分离出的三萜皂苷之一。施密特通过诱导细胞凋亡具有抗肿瘤潜力。在本研究中,我们发现黄藻糖苷II抑制MPNST细胞系ST88-14和S462的增殖并促进其凋亡。此外,这项研究提供了一种机制,通过这种机制,血红素加氧酶-1通过细胞外信号调节激酶-1/2和p38丝裂原活化的蛋白激酶途径的下调参与了黄藻糖苷II的凋亡作用。这项研究表明,弗拉西多甙II作为MPNST的新型药物治疗方法具有潜力。

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