BIOFORGE (Group for Advanced Materials and Nanobiotechnology), CIBER-BBN, University of Valladolid, Valladolid, Spain.
BIOFORGE (Group for Advanced Materials and Nanobiotechnology), CIBER-BBN, University of Valladolid, Valladolid, Spain.
Cancer Lett. 2020 Feb 1;470:43-53. doi: 10.1016/j.canlet.2019.11.031. Epub 2019 Nov 29.
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.
癌症的复杂性和不断演变使得设计新的治疗策略成为生物医学领域的一项持续挑战。此外,大多数癌症治疗方法仍然不是针对肿瘤的,并且会引起高全身性毒性。在此,我们开发了一种新型的选择性纳米器件,以消除肿瘤细胞,同时保持健康细胞完整。为了实现这一目标,测试了一种由弹性蛋白样重组体共价连接到适体并与治疗性 DNA 复合的多聚物载体。由于该载体特异性结合肿瘤细胞标志物,并在人乳腺癌细胞中选择性表达治疗性 DNA,因此形成了具有双重锁定多功能的设备。由于 ELRs 提供的稳定性,获得的均匀多聚物群体在体外和体内试验中对癌细胞表现出选择性毒性。早期检测到肿瘤进展的抑制作用,在终点时非常显著,肿瘤质量呈剂量依赖性降低。组织学研究显示肿瘤实质和特定肿瘤细胞标志物的特异性减少。这些结果代表着朝着合理开发高效、安全和更专门的肿瘤治疗基因传递装置迈出了重要一步。