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A double safety lock tumor-specific device for suicide gene therapy in breast cancer

机译:一种双安全锁定肿瘤特异性装置,用于乳腺癌的自杀基因治疗

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The complexity and continuous evolution of cancer make the design of novel strategies of treatment a constant challenge in biomedicine. Moreover, most of cancer treatments are still not tumor-specific and provoke high systemic toxicity. Herein we have developed a novel selective nanodevice to eliminate tumor cells while leaving healthy ones intact. To achieve this objective, a polyplex carrier, comprising an elastin like-recombinamer covalently conjugated to an aptamer and complexed with therapeutic DNA, was tested. This carrier forms a double-lock multifunctional device due to specific binding to a tumor cell marker and the selective expression of therapeutic DNA inside human breast-cancer cells. Due to the stability provided by ELRs, the homogeneous population of polyplexes obtained showed selective toxicity against cancer cells in in vitro and in vivo assay. Inhibition of tumor progression was detected early being very significant at the end point, with a dose-dependent reduction in tumor mass. Histological studies revealed a specific reduction in tumor parenchyma and in specific tumor cell markers. These results represent an important step toward the rational development of an efficient, safe and more specialized gene-delivery device for tumor therapy.
机译:癌症的复杂性和持续演化使得生物医学持续挑战的新策略设计。此外,大多数癌症治疗仍然不是肿瘤特异性的,并引起高系统毒性。在此,我们开发了一种新颖的选择性纳米型,以消除肿瘤细胞,同时保持健康的细胞。为了达到该目标,测试包含与适体缀合并与治疗DNA络合的弹性蛋白相似的重组体的多分布载体。由于与肿瘤细胞标记物的特异性结合和人乳腺癌细胞内的治疗性DNA的选择性表达,该载体形成双锁多功能装置。由于ELRS提供的稳定性,所获得的均相群体群体在体外和体内测定中对癌细胞进行了选择性毒性。在终点处早点检测到肿瘤进展的抑制,肿瘤质量的剂量依赖性降低。组织学研究表明肿瘤实质和特异性肿瘤细胞标志物的特异性降低。这些结果代表了朝向肿瘤疗法的有效,安全和更专业的基因输送装置的合理发育的重要一步。

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