靶向 Nrf2/PHKG2 轴,提高 NSCLC 的放射敏感性。

IF 6.8 1区 医学 Q1 ONCOLOGY NPJ Precision Oncology Pub Date : 2024-08-21 DOI:10.1038/s41698-024-00629-3
Fushi Han, Shuzhen Chen, Kangwei Zhang, Kunming Zhang, Meng Wang, Peijun Wang
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引用次数: 0

摘要

尽管铁突变有望成为抗癌策略,但人们对这一过程背后的分子机制仍然知之甚少。我们的研究旨在强调通过NRF2/PHKG2轴介导的机制调控放疗诱导的非小细胞肺癌(NSCLC)铁突变。为了鉴定与NSCLC放射耐药性相关的铁突变相关基因,本研究采用了高通量转录组测序和Lasso风险回归分析。对临床样本进行了分析,以确认放疗前后 PHKG2 表达的变化。研究进一步检测了接受放射照射的NSCLC细胞中嗜铁蛋白相关因子、细胞内铁水平、线粒体功能和铁突变,以探讨PHKG2对放射敏感性或放射抗性的影响。研究还证明了NRF2对PHKG2的转录抑制作用,并建立了NSCLC原位移植肿瘤模型,以研究NRF2/PHKG2轴在体内NSCLC放射敏感性和耐药性中的作用。纳入铁突变相关基因的Lasso风险回归模型能有效预测NSCLC患者的预后。放疗敏感组织的PHKG2表达量增加。PHKG2的过表达通过促进噬铁蛋白和增加放疗诱导的线粒体应激依赖性铁突变,导致细胞内铁水平升高。PHKG2 的转录抑制是通过 NRF2 实现的。FAGs-Lasso风险回归模型可准确预测NSCLC患者的预后。靶向Nrf2可上调PHKG2的表达,并通过促进铁自噬和诱导线粒体功能障碍逆转NSCLC的放疗耐药,从而提高放疗敏感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Targeting Nrf2/PHKG2 axis to enhance radiosensitivity in NSCLC
While ferroptosis shows promise in anti-cancer strategy, the molecular mechanisms behind this process remain poorly understood. Our research aims to highlight the regulation of radiotherapy-induced ferroptosis in non-small cell lung cancer (NSCLC) via the NRF2/PHKG2 axis-mediated mechanism. To identify ferroptosis-associated genes associated with radioresistance in NSCLC, this study employed high-throughput transcriptome sequencing and Lasso risk regression analysis. Clinical samples were analyzed to confirm PHKG2 expression changes before and after radiotherapy. The study further examined ferritinophagy-related factors, intracellular iron levels, mitochondrial function, and ferroptosis in NSCLC cells undergoing radiation exposure to explore the effect of PHKG2 on radiosensitivity or radioresistance. The research also demonstrated the transcriptional inhibition of PHKG2 by NRF2 and created in situ transplantation tumor models of NSCLC to examine the role of NRF2/PHKG2 axis in NSCLC radiosensitivity and resistance in vivo. The Lasso risk regression model that incorporated ferroptosis-associated genes effectively predicted the prognosis of patients with NSCLC. Radiotherapy-sensitive tissues exhibited an increased expression of PHKG2. Overexpression of PHKG2 led to elevated intracellular iron levels by promoting ferritinophagy and increased mitochondrial stress-dependent ferroptosis induced by radiotherapy. PHKG2 transcription repression was achieved through NRF2. The FAGs-Lasso risk regression model can accurately predict the prognosis of NSCLC patients. Targeting Nrf2 upregulates the expression of PHKG2 and reverses radiotherapy resistance in NSCLC by promoting iron autophagy and inducing mitochondrial dysfunction, thereby increasing radiotherapy sensitivity.
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来源期刊
CiteScore
9.90
自引率
1.30%
发文量
87
审稿时长
18 weeks
期刊介绍: Online-only and open access, npj Precision Oncology is an international, peer-reviewed journal dedicated to showcasing cutting-edge scientific research in all facets of precision oncology, spanning from fundamental science to translational applications and clinical medicine.
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