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首页> 外文期刊>Nanoscale >One-stop radiotherapeutic targeting of primary and distant osteosarcoma to inhibit cancer progression and metastasis using 2DG-grafted graphene quantum dots
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One-stop radiotherapeutic targeting of primary and distant osteosarcoma to inhibit cancer progression and metastasis using 2DG-grafted graphene quantum dots

机译:一站式小学和放射疗法的目标遥远的骨肉瘤抑制癌症使用2 dg-grafted进展和转移石墨烯量子点

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The application of radiotherapy (RT) to treat osteosarcoma (OS) has been limited, but this is starting to change as the ability to target radiation energy to niches improves. Furthermore, lung cancer from highly metastatic OS is a major cause of death, so it is critical to explore new strategies to tackle metastasis. In this study, we designed a nanoscale radiosensitizer by grafting 2-deoxy-d-glucose (2DG) onto graphene quantum dots (GQD) to achieve OS targeting and boost RT efficacy. Combining the use of 2DG-grafted GQDs (2DG-g-GQD) with RT produced a significant increase in oxidative stress response and DNA damage in the 143B OS cell line compared with RT alone. Moreover, 2DG-g-GQDs selectively associated with 143B cells, and demonstrated the inhibition of migration in a scratch assay. We also demonstrated remarkable improvement in their ability to inhibit tumour progression and lung metastasis in an OS xenograft mouse model. Our results show that the use of 2DG-g-GQDs as OS-targeting radiosensitizers improves their therapeutic outcome and exhibits potential for use in low-dose precision RT for OS.
机译:放疗(RT)治疗中的应用骨肉瘤(OS)是有限的,但这是开始改变的能力目标辐射能量领域改善。从高转移性肺癌的操作系统是一个主要的死因,因此探索新的至关重要解决转移策略。我们设计了一个纳米级辐射敏化剂石墨烯上嫁接2-deoxy-d-glucose (2 dg)量子点(GQD)实现系统目标提高RT功效。2 dg-grafted GQDs (2 dg-g-gqd)和RT产生了显著增加氧化应激反应143 b和DNA损伤OS细胞系相比单独使用RT。与143 b细胞,证明了迁移的抑制试验。还演示了他们的显著改善能够抑制肿瘤进展和肺一个操作系统异种移植小鼠模型中转移。结果表明,2 dg-g-gqds的使用OS-targeting辐射敏化剂提高了他们治疗结果和展品的潜力操作系统中使用低剂量精度RT。

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