Cold plasma-treated medium preferentially eliminates doxorubicin-resistant osteosarcoma cells

被引:1
|
作者
Tornin, Juan [1 ,2 ]
Gallego, Borja [1 ,2 ]
Rey, Veronica [1 ,2 ,3 ]
Murillo, Dzohara [1 ,2 ]
Huergo, Carmen [1 ,2 ]
Rodriguez, Aida [1 ,2 ]
Canal, Cristina [4 ,5 ,6 ]
Rodriguez, Rene [1 ,2 ,3 ]
机构
[1] Hosp Univ Cent Asturias, Sarcomas & Expt Therapeut Lab, Inst Invest Sanitaria Principado Asturias ISPA, Ave Roma,s-n, Oviedo 33011, Spain
[2] Inst Univ Oncol Principado Asturias, Oviedo 33011, Spain
[3] CIBER oncol CIBERONC, Madrid 28029, Spain
[4] Univ Polite cn Catalunya BarcelonaTECH UPC, Res Ctr Biomed Engn, Mat Sci & Engn Dept, Biomat Biomech & Tissue Engn Grp, C-Eduard Maristany 14, Barcelona 08019, Spain
[5] Inst Recerca Sant Joan Deu, Barcelona 08034, Spain
[6] UPC, Barcelona Res Ctr Multiscale Sci & Engn, Barcelona 08019, Spain
关键词
Osteosarcoma; Cold atmospheric plasma; Oxidative stress; Doxorubicin; Drug-resistance; CANCER; DEATH;
D O I
10.1016/j.freeradbiomed.2023.10.394
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Osteosarcoma (OS) is an aggressive bone cancer with poor prognosis, largely due to the limited effectiveness of current treatments such as doxorubicin (DX). Developing ways to overcome DX resistance is a significant clinical challenge. Here, we used two DX-resistant models to study the potential of Cold Plasma Treated Medium (PTM) to prevent DX resistance in OS. During the acquisition of the resistant phenotype upon long-term DX exposure, OS resistant cells became less proliferative, overexpressed the drug resistance-related efflux pump MDR1 and displayed a concomitant loss of SOD2 or GPX1. According to the reduced expression of these antioxidant enzymes, PTM treatment produced higher levels of oxidative express and was more effective in eradicating DXresistant cells. Moreover, PTM reduced the expression of MDR1, thus sensitizing resistant cells to DX. These findings uncover new vulnerabilities of DX-resistant cells related with their inability to cope with excessive oxidative stress and their dependence on MDR1 that can be exploited using PTM-based treatments to provide new therapeutic approaches for the management of drug resistance in OS.
引用
收藏
页码:127 / 134
页数:8
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