Morais Mariana, Machado Vera, Figueiredo Patrícia, Dias Francisca, Craveiro Rogéria, Lencart Joana, Palmeira Carlos, Mikkonen Kirsi S, Teixeira Ana Luísa, Medeiros Rui
Molecular Oncology and Viral Pathology Group, Research Center of IPO Porto (CI-IPOP)/RISE@CI-IPOP (Health Research Network), Portuguese Oncology Institute of Porto (IPO-Porto)/Porto Comprehensive Cancer Center (Porto.CCC), Research Center-LAB2, E Bdg 1st Floor, Rua Dr António Bernardino de Almeida, 4200-072 Porto, Portugal.
ICBAS, Abel Salazar Institute for the Biomedical Sciences, University of Porto, Rua Jorge Viterbo Ferreira 228, 4050-513 Porto, Portugal.
Antioxidants (Basel). 2023 Nov 28;12(12):2051. doi: 10.3390/antiox12122051.
Nanomedicine's advent has promised to revolutionize different biomedical fields, including oncology. Silver Nanoparticles (AgNPs) showed promising results in different tumor models. Clear cell Renal Cell Carcinoma (ccRCC) is especially challenging due to its late diagnosis, poor prognosis and treatment resistance. Therefore, defining new therapeutic targets and regimens could improve patient management. This study intends to evaluate AgNPs' effect in ccRCC cells and explore their potential combinatory effect with Everolimus and Radiotherapy. AgNPs were synthesized, and their effect was evaluated regarding their entering pathway, cellular proliferation capacity, ROS production, mitochondrial membrane depolarization, cell cycle analysis and apoptosis assessment. AgNPs were combined with Everolimus or used to sensitize cells to radiotherapy. AgNPs are cytotoxic to 786-O cells, a ccRCC cell line, entering through endocytosis, increasing ROS, depolarizing mitochondrial membrane, and blocking the cell cycle, leading to a reduction of proliferation capacity and apoptosis. Combined with Everolimus, AgNPs reduce cell viability and inhibit proliferation capacity. Moreover, 786-O is intrinsically resistant to radiation, but after AgNPs' administration, radiation induces cytotoxicity through mitochondrial membrane depolarization and S phase blockage. These results demonstrate AgNPs' cytotoxic potential against ccRCC and seem promising regarding the combination with Everolimus and sensitization to radiotherapy, which can, in the future, benefit ccRCC patients' management.
纳米医学的出现有望给包括肿瘤学在内的不同生物医学领域带来变革。银纳米颗粒(AgNPs)在不同的肿瘤模型中显示出了有前景的结果。肾透明细胞癌(ccRCC)因其诊断较晚、预后较差和治疗抵抗性而尤其具有挑战性。因此,确定新的治疗靶点和方案可以改善患者管理。本研究旨在评估AgNPs对ccRCC细胞的作用,并探索它们与依维莫司和放疗的潜在联合作用。合成了AgNPs,并从其进入途径、细胞增殖能力、活性氧产生、线粒体膜去极化、细胞周期分析和凋亡评估等方面对其作用进行了评估。将AgNPs与依维莫司联合使用或用于使细胞对放疗敏感。AgNPs对ccRCC细胞系786 - O具有细胞毒性,通过内吞作用进入细胞,增加活性氧,使线粒体膜去极化,并阻断细胞周期,导致增殖能力降低和细胞凋亡。与依维莫司联合使用时,AgNPs降低细胞活力并抑制增殖能力。此外,786 - O对辐射具有内在抗性,但在给予AgNPs后,辐射通过线粒体膜去极化和S期阻滞诱导细胞毒性。这些结果证明了AgNPs对ccRCC的细胞毒性潜力,并且在与依维莫司联合使用以及对放疗敏感化方面似乎很有前景,这在未来可能会有益于ccRCC患者的管理。