NOP58通过ddx18介导的DNA损伤修复调节非小细胞肺癌的放射敏感性。

IF 2.1 4区 医学 Q2 BIOLOGY
Yiqian Jiang, Weijun Zhang, Yanhong Bao, Fang Su, Bo Wang
{"title":"NOP58通过ddx18介导的DNA损伤修复调节非小细胞肺癌的放射敏感性。","authors":"Yiqian Jiang, Weijun Zhang, Yanhong Bao, Fang Su, Bo Wang","doi":"10.1093/jrr/rrag009","DOIUrl":null,"url":null,"abstract":"<p><p>Non-small cell lung cancer (NSCLC) constitutes 80-85% of lung cancers, with advanced cases showing a 20-30% 5-year survival rate. Radiation resistance limits radiotherapy efficacy, and the function of NOP58 in this process is unknown. This study investigated the mechanisms of NOP58 in NSCLC radioresistance. A radiation-resistant NSCLC cell line (H1299R) was established. Bioinformatic analysis of the Cancer Genome Atlas Program data revealed that high NOP58 expression correlates with poor patient prognosis. The expression levels of NOP58 and DDX18 expression were quantified via quantitative real-time polymerase chain reaction and Western blot. Radiosensitivity of H1299R cells and parental H1299 cells was assessed under irradiation (0, 2, 4, 6 and 8 Gy). Cell viability was assessed using cell counting kit-8 and colony formation assays. Apoptosis was detected by flow cytometry with Annexin V/PI staining. DNA damage was analyzed via γ-H2AX immunofluorescence and comet assays. NOP58 knockdown and DDX18 overexpression were performed for rescue experiments, and protein interaction was validated by pull-down assays. NOP58 and DDX18 were significantly upregulated in H1299R cells. H1299R cells exhibited higher cell viability, stronger colony-forming capacity, reduced apoptosis and less DNA damage under irradiation treatment. The depletion of NOP58 in H1299 and H1299R cells exacerbated radiation-induced DNA damage, reduced cell viability and promoted apoptosis, reversing radioresistance. Direct interaction between NOP58 and DDX18 was confirmed by pull-down assay. DDX18 overexpression reversed the radiosensitizing effects of NOP58 knockdown, including attenuated DNA damage and restored cell survival. Overexpression NOP58 converted radiosensitive cells to a resistant phenotype. NOP58 promotes NSCLC radioresistance by interacting with DDX18, regulating its expression and thereby suppressing radiation-induced DNA damage. The NOP58-DDX18 axis could be a promising therapeutic target for improving radiotherapy efficacy in NSCLC.</p>","PeriodicalId":16922,"journal":{"name":"Journal of Radiation Research","volume":" ","pages":"276-292"},"PeriodicalIF":2.1000,"publicationDate":"2026-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13019138/pdf/","citationCount":"0","resultStr":"{\"title\":\"NOP58 modulates radiosensitivity in non-small cell lung cancer via DDX18-mediated DNA damage repair.\",\"authors\":\"Yiqian Jiang, Weijun Zhang, Yanhong Bao, Fang Su, Bo Wang\",\"doi\":\"10.1093/jrr/rrag009\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Non-small cell lung cancer (NSCLC) constitutes 80-85% of lung cancers, with advanced cases showing a 20-30% 5-year survival rate. Radiation resistance limits radiotherapy efficacy, and the function of NOP58 in this process is unknown. This study investigated the mechanisms of NOP58 in NSCLC radioresistance. A radiation-resistant NSCLC cell line (H1299R) was established. Bioinformatic analysis of the Cancer Genome Atlas Program data revealed that high NOP58 expression correlates with poor patient prognosis. The expression levels of NOP58 and DDX18 expression were quantified via quantitative real-time polymerase chain reaction and Western blot. Radiosensitivity of H1299R cells and parental H1299 cells was assessed under irradiation (0, 2, 4, 6 and 8 Gy). Cell viability was assessed using cell counting kit-8 and colony formation assays. Apoptosis was detected by flow cytometry with Annexin V/PI staining. DNA damage was analyzed via γ-H2AX immunofluorescence and comet assays. NOP58 knockdown and DDX18 overexpression were performed for rescue experiments, and protein interaction was validated by pull-down assays. NOP58 and DDX18 were significantly upregulated in H1299R cells. H1299R cells exhibited higher cell viability, stronger colony-forming capacity, reduced apoptosis and less DNA damage under irradiation treatment. The depletion of NOP58 in H1299 and H1299R cells exacerbated radiation-induced DNA damage, reduced cell viability and promoted apoptosis, reversing radioresistance. Direct interaction between NOP58 and DDX18 was confirmed by pull-down assay. DDX18 overexpression reversed the radiosensitizing effects of NOP58 knockdown, including attenuated DNA damage and restored cell survival. Overexpression NOP58 converted radiosensitive cells to a resistant phenotype. NOP58 promotes NSCLC radioresistance by interacting with DDX18, regulating its expression and thereby suppressing radiation-induced DNA damage. The NOP58-DDX18 axis could be a promising therapeutic target for improving radiotherapy efficacy in NSCLC.</p>\",\"PeriodicalId\":16922,\"journal\":{\"name\":\"Journal of Radiation Research\",\"volume\":\" \",\"pages\":\"276-292\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2026-03-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13019138/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Radiation Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/jrr/rrag009\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Radiation Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/jrr/rrag009","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

非小细胞肺癌(NSCLC)占肺癌的80-85%,晚期病例的5年生存率为20-30%。放射抵抗限制了放疗效果,而NOP58在这一过程中的作用尚不清楚。本研究探讨了NOP58在NSCLC放射耐药中的作用机制。建立了耐辐射NSCLC细胞株H1299R。癌症基因组图谱项目数据的生物信息学分析显示,NOP58高表达与患者预后差相关。通过实时荧光定量聚合酶链反应和Western blot检测NOP58和DDX18的表达水平。在0、2、4、6和8 Gy的辐照下,评估H1299R细胞和亲本H1299细胞的放射敏感性。采用细胞计数试剂盒-8和菌落形成试验评估细胞活力。Annexin V/PI染色流式细胞术检测细胞凋亡。通过γ-H2AX免疫荧光和彗星分析DNA损伤。进行NOP58敲低和DDX18过表达的救援实验,并通过下拉实验验证蛋白相互作用。NOP58和DDX18在H1299R细胞中显著上调。H1299R细胞在辐照下表现出更高的细胞活力、更强的集落形成能力、更少的凋亡和更小的DNA损伤。H1299和H1299R细胞中NOP58的缺失加重了辐射诱导的DNA损伤,降低了细胞活力,促进了细胞凋亡,逆转了辐射耐药。下拉实验证实了NOP58与DDX18的直接相互作用。DDX18过表达逆转了NOP58敲低的放射增敏作用,包括减轻DNA损伤和恢复细胞存活。过表达NOP58将辐射敏感细胞转化为抗性表型。NOP58通过与DDX18相互作用,调节其表达,从而抑制辐射诱导的DNA损伤,从而促进NSCLC的放射耐药。NOP58-DDX18轴有望成为提高NSCLC放疗疗效的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

NOP58 modulates radiosensitivity in non-small cell lung cancer via DDX18-mediated DNA damage repair.

NOP58 modulates radiosensitivity in non-small cell lung cancer via DDX18-mediated DNA damage repair.

NOP58 modulates radiosensitivity in non-small cell lung cancer via DDX18-mediated DNA damage repair.

NOP58 modulates radiosensitivity in non-small cell lung cancer via DDX18-mediated DNA damage repair.

Non-small cell lung cancer (NSCLC) constitutes 80-85% of lung cancers, with advanced cases showing a 20-30% 5-year survival rate. Radiation resistance limits radiotherapy efficacy, and the function of NOP58 in this process is unknown. This study investigated the mechanisms of NOP58 in NSCLC radioresistance. A radiation-resistant NSCLC cell line (H1299R) was established. Bioinformatic analysis of the Cancer Genome Atlas Program data revealed that high NOP58 expression correlates with poor patient prognosis. The expression levels of NOP58 and DDX18 expression were quantified via quantitative real-time polymerase chain reaction and Western blot. Radiosensitivity of H1299R cells and parental H1299 cells was assessed under irradiation (0, 2, 4, 6 and 8 Gy). Cell viability was assessed using cell counting kit-8 and colony formation assays. Apoptosis was detected by flow cytometry with Annexin V/PI staining. DNA damage was analyzed via γ-H2AX immunofluorescence and comet assays. NOP58 knockdown and DDX18 overexpression were performed for rescue experiments, and protein interaction was validated by pull-down assays. NOP58 and DDX18 were significantly upregulated in H1299R cells. H1299R cells exhibited higher cell viability, stronger colony-forming capacity, reduced apoptosis and less DNA damage under irradiation treatment. The depletion of NOP58 in H1299 and H1299R cells exacerbated radiation-induced DNA damage, reduced cell viability and promoted apoptosis, reversing radioresistance. Direct interaction between NOP58 and DDX18 was confirmed by pull-down assay. DDX18 overexpression reversed the radiosensitizing effects of NOP58 knockdown, including attenuated DNA damage and restored cell survival. Overexpression NOP58 converted radiosensitive cells to a resistant phenotype. NOP58 promotes NSCLC radioresistance by interacting with DDX18, regulating its expression and thereby suppressing radiation-induced DNA damage. The NOP58-DDX18 axis could be a promising therapeutic target for improving radiotherapy efficacy in NSCLC.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
3.60
自引率
5.00%
发文量
86
审稿时长
4-8 weeks
期刊介绍: The Journal of Radiation Research (JRR) is an official journal of The Japanese Radiation Research Society (JRRS), and the Japanese Society for Radiation Oncology (JASTRO). Since its launch in 1960 as the official journal of the JRRS, the journal has published scientific articles in radiation science in biology, chemistry, physics, epidemiology, and environmental sciences. JRR broadened its scope to include oncology in 2009, when JASTRO partnered with the JRRS to publish the journal. Articles considered fall into two broad categories: Oncology & Medicine - including all aspects of research with patients that impacts on the treatment of cancer using radiation. Papers which cover related radiation therapies, radiation dosimetry, and those describing the basis for treatment methods including techniques, are also welcomed. Clinical case reports are not acceptable. Radiation Research - basic science studies of radiation effects on livings in the area of physics, chemistry, biology, epidemiology and environmental sciences. Please be advised that JRR does not accept any papers of pure physics or chemistry. The journal is bimonthly, and is edited and published by the JRR Editorial Committee.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书