Institute of Polymers, Composites and Biomaterials , National Research Council (IPCB-CNR) , Mostra d'Oltremare pad.20-Viale J.F. Kennedy 54 , 80125 Naples , Italy.
Institute of Chemistry of Organometallic Compounds , National Research Council (ICCOM-CNR) , via Madonna del Piano 10 , 50019 Sesto Fiorentino , Italy.
ACS Appl Mater Interfaces. 2019 Mar 6;11(9):9333-9342. doi: 10.1021/acsami.8b21592. Epub 2019 Feb 22.
Nowadays chemotherapy is the main treatment for osteosarcoma disease, even if limited by the lack of selectivity between healthy and cancer cells during the inhibition of cell division. Herein, we propose the use of few-layer two-dimensional black phosphorous (2D bP) as an alternative tool for osteosarcoma treatment and report how 2D bP can stimulate newly forming bone tissue generation after osteosarcoma resection. In our study, we have developed an in vitro model to evaluate the efficacy of 2D bP material with and without near-infrared light irradiation treatment, and we have demonstrated that the presence of 2D bP without treatment inhibits the metabolic activity of osteosarcoma cells (SAOS-2) while inducing both the proliferation and the osteogenic differentiation of human preosteoblast cells (HOb) and mesenchymal stem cells. Furthermore, we also propose an in vitro coculture model (SAOS-2 and HOb cell lines) in order to study the effect of 2D bP on inflammatory response related to cancer. On this coculture model, 2D bP may increase anti-inflammatory cytokine generation (i.e., interleukin-10) and inhibit proinflammatory mediators synthesis (i.e., interleukin-6), thus suggesting the opportunity to prevent cancer-related inflammation. Finally, we have demonstrated that 2D bP represents a promising candidate for future regenerative medicine and anticancer applications.
如今,化疗是骨肉瘤疾病的主要治疗方法,即使在抑制细胞分裂过程中,健康细胞和癌细胞之间的选择性受到限制。在此,我们提出使用少层二维黑磷(2D bP)作为骨肉瘤治疗的替代工具,并报告 2D bP 如何在骨肉瘤切除后刺激新形成的骨组织生成。在我们的研究中,我们开发了一种体外模型来评估具有和不具有近红外光照射治疗的 2D bP 材料的功效,我们已经证明,在没有治疗的情况下存在 2D bP 会抑制骨肉瘤细胞(SAOS-2)的代谢活性,同时诱导人成骨前体细胞(HOb)和间充质干细胞的增殖和成骨分化。此外,我们还提出了一种体外共培养模型(SAOS-2 和 HOb 细胞系),以研究 2D bP 对与癌症相关的炎症反应的影响。在这个共培养模型中,2D bP 可以增加抗炎细胞因子的产生(即白细胞介素-10)并抑制促炎介质的合成(即白细胞介素-6),从而为预防癌症相关炎症提供了机会。最后,我们已经证明 2D bP 是未来再生医学和抗癌应用的有前途的候选者。