{"title":"Cold plasma with zirconia nanoparticles for lung cancer via TGF-\\b{eta} signaling pathway","authors":"Yueye Huang, Rui Zhang, Xiao Chen, Fei Cao, Qiujie Fang, Qingnan Xu, Shicong Huang, Yufan Wang, Guojun Chen, Zhitong Chen","doi":"arxiv-2408.11838","DOIUrl":null,"url":null,"abstract":"Despite advancements in lung cancer therapy, the prognosis for advanced or\nmetastatic patients remains poor, yet many patients eventually develop\nresistance to standard treatments leading to disease progression and poor\nsurvival. Here, we described a combination of CAP and nanoparticles (ZrO2 NPs\n(zirconium oxide nanoparticle) and 3Y-TZP NPs (3% mol Yttria Tetragonal\nZirconia Polycrystal Nanoparticle)) for lung cancer therapy. We found that ZrO2\nNPs caused obvious damage to the inside of the lung cancer cells. CAP and ZrO2\nNPs mainly affected the mitochondria function, leading to a decrease in\nmitochondrial membrane potential and ATP levels, and causing endoplasmic\nreticulum stress and cell nucleus internal DNA damage, etc. CAP combined with\nZrO2 NPs (CAP@ZrO2) induced lung cancer cell apoptosis by activating the\nTGF-\\b{eta} pathway. CAP@ZrO2 offers a new therapy for the clinical treatment\nof lung cancer.","PeriodicalId":501378,"journal":{"name":"arXiv - PHYS - Medical Physics","volume":"60 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - PHYS - Medical Physics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2408.11838","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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.