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A novel synthetic oleanane triterpenoid suppresses adhesion migration and invasion of highly metastatic melanoma cells by modulating gelatinase signaling axis

机译:新型合成齐墩果烷三萜通过调节明胶酶信号转导轴抑制高转移性黑色素瘤细胞的粘附迁移和侵袭

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摘要

BackgroundA methyl derivative natural triterpenoid amooranin (methyl-25-hydroxy-3-oxoolean-12-en-28-oate, AMR-Me) has been found to possess antiproliferative, proapoptotic and anti-inflammatory effects against established tumor cells. Large-scale synthesis of pure AMR-Me has eliminated the need of the natural phytochemical for further development of AMR-Me as an anticancer drug. Metastatic melanoma is a fatal form of cutaneous malignancy with poor prognosis and limited therapeutic options. It was hypothesized that antitumor pharmacological effect of AMR-Me could be linked to AMR-Me-mediated suppression of the metastatic potential of B16F10 murine melanoma.
机译:背景技术已发现甲基衍生物天然三萜类阿米拉宁(甲基25-羟基-3-氧代氧杂十二烷基-en-28-酸酯,AMR-Me)对已建立的肿瘤细胞具有抗增殖,促凋亡和抗炎作用。纯AMR-Me的大规模合成消除了天然植物化学物质对进一步开发AMR-Me作为抗癌药物的需求。转移性黑色素瘤是致命的皮肤恶性肿瘤,预后不良,治疗选择有限。据推测,AMR-Me的抗肿瘤药理作用可能与AMR-Me介导的B16F10鼠黑色素瘤转移潜能的抑制有关。

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