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冷等离体子体与氧化铁基磁性纳米颗粒协同治疗肺癌。

Cold atmospheric plasma and iron oxide-based magnetic nanoparticles for synergetic lung cancer therapy.

机构信息

Department of Pathology, Weifang Medical University, Weifang, Shandong 261053, China.

Department of pharmaceutics, Weifang Medical University, Weifang, Shandong 261053, China.

出版信息

Free Radic Biol Med. 2019 Jan;130:71-81. doi: 10.1016/j.freeradbiomed.2018.10.429. Epub 2018 Oct 17.

Abstract

Cold atmospheric plasma (CAP) is an emerging biomedical technique that shows great potential for cancer treatment. On the other hand, magnetic nanoparticles open up a wide field of possible applications in medicine. Here we seek to develop a novel dual cancer therapeutic method by integrating promising CAP and iron oxide-based magnetic nanoparticles (MNPs), and evaluate its underlying mechanism for targeted lung cancer treatment. For this purpose, the synergistic effects of CAP and iron oxide-based MNPs on cellular bioactivity, epidermal growth factor receptor (EGFR) expression, and EGFR downstream signaling pathways were investigated. Results showed that the effectiveness of CAP and iron oxide-based MNPs for synergistic strongly killed activity against lung cancer cells, and significantly inhibited cell proliferation via reduction of viability and induction of apoptosis. Importantly, CAP combining with iron oxide-based MNPs induced EGFR downregulation while CAP inhibited lung cancer cells via depressing pERK and pAKT. Translation of these findings to an in vivo setting demonstrates that CAP combining iron oxide-based MNPs is effective at preventing xenograft tumors. Thus, the integration of CAP and iron oxide-based MNPs provides a promising tool for the development of a new cancer treatment strategy.

摘要

低温常压等离子体(CAP)是一种新兴的生物医学技术,在癌症治疗方面显示出巨大的潜力。另一方面,磁性纳米颗粒为医学的应用开辟了广阔的领域。在这里,我们试图通过整合有前途的 CAP 和基于氧化铁的磁性纳米颗粒(MNP)来开发一种新的双重癌症治疗方法,并评估其靶向肺癌治疗的潜在机制。为此,研究了 CAP 和基于氧化铁的 MNP 对细胞生物活性、表皮生长因子受体(EGFR)表达和 EGFR 下游信号通路的协同作用。结果表明,CAP 和基于氧化铁的 MNP 的协同作用对肺癌细胞具有强烈的杀伤活性,通过降低细胞活力和诱导细胞凋亡,显著抑制细胞增殖。重要的是,CAP 联合基于氧化铁的 MNP 诱导 EGFR 下调,而 CAP 通过抑制 pERK 和 pAKT 抑制肺癌细胞。将这些发现转化为体内环境表明,CAP 联合基于氧化铁的 MNP 可有效预防异种移植肿瘤。因此,CAP 和基于氧化铁的 MNP 的整合为开发新的癌症治疗策略提供了有前途的工具。

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