Plasma‐Activated Saline Resensitizes Cisplatin‐Resistant T24 Bladder Cancer Cells

IF 3.2 3区 物理与天体物理 Q2 PHYSICS, APPLIED
Zewei Wang, Zimu Yu, He Zhu, Xixi Jing, Dingxin Liu, Hao Zhang, Xin Yang, Renwu Zhou, Mingzhe Rong
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引用次数: 0

Abstract

ABSTRACT Plasma‐activated saline (PAS) loads reactive oxygen and nitrogen species, triggering oxidative stress and tumor death. However, PAS exhibits poor anticancer efficacy due to rapid dilution and reactive species decay. Herein, we developed a plasma bubble reactor to activate saline and investigate its synergy with cisplatin (DDP) against DDP‐resistant T24 bladder cancer cells (T24/DDP) in vitro. The results showed that PAS‐DDP significantly reduced the cell viability of T24/DDP to 32.4%, surpassing PAS (52.9%) or DDP alone (96.9%). PAS‐DDP significantly inhibited T24/DDP cells by intracellular reactive oxygen species accumulation, mitochondrial depolarization, and cell apoptosis induction. Moreover, PAS‐DDP suppressed the p62/Keap1/Nrf2 signaling pathway, restoring oxidative sensitivity and boosting DDP efficacy. These findings suggest that PAS could enhance chemotherapy efficacy and overcome drug resistance.
血浆活化盐水使顺铂耐药T24膀胱癌细胞重致敏
血浆活化盐水(PAS)负荷活性氧和活性氮,引发氧化应激和肿瘤死亡。然而,由于稀释迅速和反应性物质衰变,PAS表现出较差的抗癌功效。在此,我们开发了一个血浆泡反应器来激活生理盐水,并研究其与顺铂(DDP)在体外对耐药的T24膀胱癌细胞(T24/DDP)的协同作用。结果表明,PAS‐DDP显著降低了T24/DDP的细胞活力,达到32.4%,超过了PAS(52.9%)或DDP单独(96.9%)。PAS‐DDP通过细胞内活性氧积累、线粒体去极化和细胞凋亡诱导显著抑制T24/DDP细胞。此外,PAS‐DDP抑制p62/Keap1/Nrf2信号通路,恢复氧化敏感性并提高DDP的疗效。这些发现提示PAS可提高化疗疗效,克服耐药。
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来源期刊
Plasma Processes and Polymers
Plasma Processes and Polymers 物理-高分子科学
CiteScore
6.60
自引率
11.40%
发文量
150
审稿时长
3 months
期刊介绍: Plasma Processes & Polymers focuses on the interdisciplinary field of low temperature plasma science, covering both experimental and theoretical aspects of fundamental and applied research in materials science, physics, chemistry and engineering in the area of plasma sources and plasma-based treatments.
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