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Gemcitabine, vinorelbine and cyclooxygenase inhibitors in the treatment of glioblastoma. Ultrastructural analyses in C6 glioma in vitro

机译:吉西他滨,血红素和环加氧酶抑制剂治疗胶质母细胞瘤。 C6胶质瘤的超微结构分析体外

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Objectives: To define ultrastructural features accompanying to antitumor effects of gemcitabine, vinorelbine and cyclooxygenase inhibitors in C6 glioma cells in vitro. Vinorelbine is a semisynthetic vinca alkaloid and recent studies showed its antitumor activity in pediatric optic and pontine gliomas. Vinorelbine infusion induces a severe tumor site-pain in systemic cancers, but it is unknown whether algesia and inflammation contribute to its antitumor effects. Gemcitabine is a nucleoside-chemotherapeutic which was recently shown to act as a radiosensitizer in high-grade glioma. Some studies showed synergism of anti-inflammatory cyclooxygenase-inhibitors with microtubule inhibitors and gemcitabine. DMSO is a solvent and blocks both cylooxygenase and ribonucleotide reductase, another target of gemcitabine. Rofecoxib is withdrawn from the market, yet we used it for investigational purposes, since it blocks cylooxygenase-2 1000-times more potently than cylooxygenase-1 and is also a selective inhibitor of crinophagy.
机译:目的:以伴随着吉西他滨,血列林和环氧树脂酶抑制剂在体外C6胶质瘤细胞中的抗肿瘤作用的超微结构特征。 Vinorelbine是一个半合成的vinca生物碱,最近的研究表明其在小儿视神经和猪胶质瘤中的抗肿瘤活性。血肠输注诱导全身癌症严重的肿瘤疼痛,但艾尔腓和炎症是未知的抗肿瘤效应。吉西他滨是一种核苷 - 化学治疗性,最近显示在高级胶质瘤中作为辐射敏化剂。一些研究表明,具有微管抑制剂和吉西他滨的抗炎环氧化酶抑制剂的协同作用。 DMSO是一种溶剂,并阻止硅氧烷酶和核糖核苷酸还原酶,吉西他滨的另一种靶标。 ROFecoxib从市场中撤回,但我们使用它用于调查目的,因为它会使圆柱氧酶-2比圆柱氧酶-1更易于效果,并且也是溃噬细胞的选择性抑制剂。

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