首页> 外文期刊>Acta Biochimica Polonica >Combination of IL-12 gene therapy and CTX chemotherapy inhibits growth of primary B16(F10) melanoma tumors in mice
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Combination of IL-12 gene therapy and CTX chemotherapy inhibits growth of primary B16(F10) melanoma tumors in mice

机译:IL-12基因治疗和CTX化疗联合抑制小鼠原发性B16(F10)黑色素瘤的生长

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We investigated suppression of murine B16(F10) melanoma tumor growth following a therapy which involved concomitant administration of cyclophosphamide and plasmid DNA bearing interleukin-12 gene. Since both therapeutic factors display antiangiogenic capabilities, we assumed that their use in blocking the formation of new blood vessels would result in augmented inhibition of tumor growth. This combined therapy regimen indeed resulted in a considerable suppression of tumor growth. We observed a statistically significant extension of treated animals' lifespan. Interestingly, the therapeutic effect was also obtained using a plasmid without an interleukin gene insert. This observation suggests that plasmid DNA, which has been widely applied for treating neoplastic tumors, contains element(s) that elicit immune response in mice.
机译:我们调查了一种治疗后对鼠B16(F10)黑色素瘤肿瘤生长的抑制,该治疗涉及同时给予环磷酰胺和携带白介素12基因的质粒DNA。由于这两种治疗因子均显示出抗血管生成的能力,因此我们假设它们在阻断新血管形成中的用途将导致对肿瘤生长的抑制作用增强。这种联合治疗方案确实导致了肿瘤生长的显着抑制。我们观察到治疗动物的寿命在统计学上显着延长。有趣的是,使用没有白介素基因插入物的质粒也获得了治疗效果。该观察结果表明,已被广泛用于治疗赘生性肿瘤的质粒DNA含有引起小鼠免疫应答的元素。

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