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Morphological transformation induced by silver nanoparticles in a Balb/c 3T3 A31-1-1 mouse cell model to evaluate in vitro carcinogenic potential

机译:银纳米颗粒在Balb / c 3T3 A31-1-1小鼠细胞模型中诱导的形态转化以评估体外致癌潜力

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摘要

Carcinogenesis is a complex process involved in genotoxic and non-genotoxic pathways. The carcinogenic potential of silver nanoparticles (AgNPs) has been predicted by examining their genotoxic effects using several in vitro and in vivo models. However, there is no little information regarding the non-genotoxic effects of AgNPs related to carcinogenesis. The in vitro cell transformation assay (CTA) provides specific and sensitive evidence for predicting the tumorigenic potential of a chemical, which cannot be obtained by genotoxicity testing. Therefore, we carried out CTA in Balb/c 3T3 A31-1-1 cells to evaluate the carcinogenic potential of AgNPs. Colony-forming efficiency and crystal violet assays were carried out to determine the cytotoxicity of AgNPs. A cytokinesis-block micronucleus (CBMN) assay and CTA were performed using Balb/c 3T3 A31-1-1 cells to predict the in vitro carcinogenic potential of AgNPs. In the CBMN assay, AgNPs (10.6 μg/mL) induced a significant increase in micronucleus formation indicating a genotoxic effect. Thus, AgNPs could be an initiator of carcinogenesis. In the CTA, used to assess the carcinogenic potential of AgNPs, cells exposed to AgNPs for 72 hours showed significantly induced morphological neoplastic transformation at all tested doses (0.17, 0.66, 2.65, 5.30, and 10.60 μg/mL), and the transformation frequency was significantly increased in a dose-dependent manner. These results indicate that short-term exposure (72 hours) to AgNPs had in vitro carcinogenetic potency in Balb/c 3T3 A31-1-1 cells.
机译:致癌作用是涉及遗传毒性和非遗传毒性途径的复杂过程。通过使用几种体外和体内模型研究银纳米颗粒的遗传毒性效应,可以预测其潜在的致癌性。但是,关于与致癌作用有关的AgNP的非遗传毒性作用的信息很少。体外细胞转化试验(CTA)为预测化学物质的致癌潜力提供了特异性和敏感的证据,而遗传毒性测试无法获得这种证据。因此,我们在Balb / c 3T3 A31-1-1细胞中进行了CTA,以评估AgNP的致癌潜力。进行菌落形成效率和结晶紫测定以确定AgNP的细胞毒性。使用Balb / c 3T3 A31-1-1细胞进行胞质分裂阻滞微核(CBMN)分析和CTA,以预测AgNP的体外致癌潜力。在CBMN分析中,AgNP(10.6μg/ mL)诱导了微核形成的显着增加,表明具有遗传毒性作用。因此,AgNPs可能是致癌的引发剂。在用于评估AgNPs致癌潜力的CTA中,暴露于AgNPs 72小时的细胞在所有测试剂量(0.17、0.66、2.65、5.30和10.60μg/ mL)下均表现出显着诱导的形态学肿瘤转化,并且转化频率以剂量依赖性方式显着增加。这些结果表明,短期(72小时)暴露于AgNPs在Balb / c 3T3 A31-1-1细胞中具有体外致癌作用。

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