冷等离子与氧化锆纳米颗粒通过 TGF-\b{eta} 信号通路治疗肺癌

Yueye Huang, Rui Zhang, Xiao Chen, Fei Cao, Qiujie Fang, Qingnan Xu, Shicong Huang, Yufan Wang, Guojun Chen, Zhitong Chen
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引用次数: 0

摘要

尽管肺癌治疗取得了进展,但晚期或转移性患者的预后仍然很差,许多患者最终会对标准治疗产生抗药性,导致疾病进展和生存率低下。在此,我们介绍了一种结合 CAP 和纳米粒子(ZrO2 NPs(氧化锆纳米粒子)和 3Y-TZP NPs(3% mol Yttria TetragonalZirconia Polycrystal Nanoparticle))的肺癌治疗方法。我们发现 ZrO2NPs 对肺癌细胞内部造成了明显的损伤。CAP 和 ZrO2NPs 主要影响线粒体功能,导致线粒体膜电位和 ATP 水平下降,引起内质网应激和细胞核内部 DNA 损伤等。CAP与ZrO2 NPs(CAP@ZrO2)通过激活TGF-\b{eta}途径诱导肺癌细胞凋亡。CAP@ZrO2为临床治疗肺癌提供了一种新疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cold plasma with zirconia nanoparticles for lung cancer via TGF-\b{eta} signaling pathway
Despite advancements in lung cancer therapy, the prognosis for advanced or metastatic patients remains poor, yet many patients eventually develop resistance to standard treatments leading to disease progression and poor survival. Here, we described a combination of CAP and nanoparticles (ZrO2 NPs (zirconium oxide nanoparticle) and 3Y-TZP NPs (3% mol Yttria Tetragonal Zirconia Polycrystal Nanoparticle)) for lung cancer therapy. We found that ZrO2 NPs caused obvious damage to the inside of the lung cancer cells. CAP and ZrO2 NPs mainly affected the mitochondria function, leading to a decrease in mitochondrial membrane potential and ATP levels, and causing endoplasmic reticulum stress and cell nucleus internal DNA damage, etc. CAP combined with ZrO2 NPs (CAP@ZrO2) induced lung cancer cell apoptosis by activating the TGF-\b{eta} pathway. CAP@ZrO2 offers a new therapy for the clinical treatment of lung cancer.
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