3rd Department of Internal Medicine, University Hospital and Faculty of Medicine, Hradec Kralove, Charles University, Hradec Kralove, Czech Republic.
Department of General and Inorganic Chemistry, Faculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.
Neoplasma. 2020 May;67(3):576-583. doi: 10.4149/neo_2020_190710N620. Epub 2020 Mar 18.
The standard therapy for malignant primary bone tumors such as osteosarcoma involves major surgeries. For tumors located in difficult regions such as the pelvis, surgical intervention could lead to serious side effects for example loss of a limb and/or function, loss of bowel, bladder and sexual function as well as problems with wound healing and surgical complications. Therefore, exploring other approaches that can improve or complement current surgical techniques is important. Hence, sensitizing primary bone tumors to radiation could offer an additional strategy that could complement surgery and significantly improve survival and quality of life. Gold nanoparticles (AuNPs) have been shown to enhance radiosensitivity by increasing the local dose of radiation inside tumors. Therefore, the referred procedure of preparation and functionalization of gold nanoparticles may be used for investigation whether DNA repair inhibition in the presence of AuNPs leads to an effective radiosensitizing strategy for primary bone tumor cells and explore the mechanism of how this may be happening. In our work, we prepared gold nanoparticles and verified the relation between the size of the AuNPs and their uptake in tumor 143B cells and also investigated whether the optimal size of the AuNPs should not be smaller than the size of nuclear envelope pores (20-50 nm). Hence, two different AuNPs systems were prepared: the first one with AuNPs core size of about 5 nm (BS) and the second one with AuNPs core size of about 50 nm (ZA). For cellular AuNPs uptake enhancement, we functionalized the AuNPs with signaling peptides. For this purpose we prepared PEG-coated AuNPs functionalized with signal peptides for targeted transport into the cytoplasm (CPP) and into the cell nucleus (CPP + NLS). The toxicity of the AuNPs systems was assessed by MTS assay. We prepared stable functionalized AuNPs systems of both sizes. With the functionalizing of the AuNPs using signal peptides (CPP, NLS), the AuNPs penetrated into the cell nucleus. The referred procedure of preparation and functionalization of gold nanoparticles may be used for investigating inhibition of DNA repair in the presence of AuNPs and it could lead to new understanding in overcoming radioresistance in primary bone tumor cells.
对于骨肉瘤等恶性原发性骨肿瘤,标准治疗包括大手术。对于位于骨盆等困难区域的肿瘤,手术干预可能会导致严重的副作用,例如失去肢体和/或功能、肠、膀胱和性功能丧失以及伤口愈合和手术并发症问题。因此,探索可以改善或补充当前手术技术的其他方法很重要。因此,使原发性骨肿瘤对辐射敏感可能提供一种额外的策略,可以补充手术,并显著提高生存率和生活质量。金纳米粒子(AuNPs)已被证明可以通过增加肿瘤内的局部辐射剂量来提高放射敏感性。因此,所提到的金纳米粒子的制备和功能化过程可用于研究在 AuNPs 存在的情况下抑制 DNA 修复是否会导致原发性骨肿瘤细胞的有效放射增敏策略,并探讨这种情况发生的机制。在我们的工作中,我们制备了金纳米粒子,并验证了 AuNPs 的大小与其在肿瘤 143B 细胞中的摄取之间的关系,还研究了 AuNPs 的最佳大小是否不应小于核包膜孔的大小(20-50nm)。因此,我们制备了两种不同的 AuNPs 体系:第一种 AuNPs 核大小约为 5nm(BS),第二种 AuNPs 核大小约为 50nm(ZA)。为了增强细胞内 AuNPs 的摄取,我们用信号肽对 AuNPs 进行了功能化。为此,我们制备了用聚乙二醇(PEG)包裹的信号肽功能化的 AuNPs,用于靶向运输到细胞质(CPP)和细胞核(CPP+NLS)。通过 MTS 测定评估了 AuNPs 体系的毒性。我们制备了两种尺寸的稳定功能化 AuNPs 体系。通过使用信号肽(CPP、NLS)对 AuNPs 进行功能化,AuNPs 穿透到细胞核中。所提到的金纳米粒子的制备和功能化过程可用于研究在 AuNPs 存在的情况下抑制 DNA 修复,这可能会导致对原发性骨肿瘤细胞放射抵抗的新认识。