WDR35 Is Associated with Chemosensitivity and Prognosis in Lung Adenocarcinoma.

IF 2.4 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Liang Tang, Yinhui Xu, Xinmiao Zhang, Tianjun Song, Yirui Wei, Haijun Zhang, Yunfei Zhou, Youshan Li
{"title":"<i>WDR35</i> Is Associated with Chemosensitivity and Prognosis in Lung Adenocarcinoma.","authors":"Liang Tang, Yinhui Xu, Xinmiao Zhang, Tianjun Song, Yirui Wei, Haijun Zhang, Yunfei Zhou, Youshan Li","doi":"10.1089/cbr.2025.0124","DOIUrl":null,"url":null,"abstract":"<p><p><b><i>Background:</i></b> This study investigates the expression characteristics of WD repeat domain 35 (<i>WDR35</i>) in lung adenocarcinoma (LUAD) and its association with chemotherapy sensitivity and prognosis. <b><i>Methods:</i></b> Differentially expressed genes were analyzed in combination with Random Forest and Support Vector Machine algorithms to identify key genes associated with chemotherapy sensitivity. The expression differences of the core gene at both transcriptomic and proteomic levels were then experimentally validated using real-world LUAD samples. Drug sensitivity analysis was conducted using the Genomics of Drug Sensitivity in Cancer database to evaluate the correlation between the core gene and the IC<sub>50</sub> values of various chemotherapeutic agents. Gene Set Enrichment Analysis (GSEA) was used to explore the potential mechanisms involved. Finally, Kaplan-Meier survival analysis and stratified analysis by tumor stage and lymph node status were performed to assess the prognostic value of the core gene. <b><i>Results:</i></b> <i>WDR35</i> as a core gene associated with chemotherapy sensitivity and highly expressed in normal lung tissue compared with tumor tissue, which was further validated at both the qPCR and proteomic levels. Clinical correlation analysis indicated that <i>WDR35</i> expression is significantly associated with tumor size, lymph node metastasis, and tumor stage. Further analysis revealed that patients with high <i>WDR35</i> expression were more likely to achieve partial or complete response to initial chemotherapy. Drug sensitivity prediction analysis demonstrated that high <i>WDR35</i> expression was significantly correlated with increased sensitivity to various anticancer drugs. GSEA pathway enrichment analysis suggested that <i>WDR35</i> may enhance chemotherapy sensitivity by regulating stress response and metabolic pathways. Survival analysis indicated that high <i>WDR35</i> expression was associated with better overall survival and disease-specific survival. <b><i>Conclusions:</i></b> Our study reveals that <i>WDR35</i> is closely associated with chemotherapy sensitivity and prognosis in lung adenocarcinoma.</p>","PeriodicalId":55277,"journal":{"name":"Cancer Biotherapy and Radiopharmaceuticals","volume":" ","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer Biotherapy and Radiopharmaceuticals","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1089/cbr.2025.0124","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

Background: This study investigates the expression characteristics of WD repeat domain 35 (WDR35) in lung adenocarcinoma (LUAD) and its association with chemotherapy sensitivity and prognosis. Methods: Differentially expressed genes were analyzed in combination with Random Forest and Support Vector Machine algorithms to identify key genes associated with chemotherapy sensitivity. The expression differences of the core gene at both transcriptomic and proteomic levels were then experimentally validated using real-world LUAD samples. Drug sensitivity analysis was conducted using the Genomics of Drug Sensitivity in Cancer database to evaluate the correlation between the core gene and the IC50 values of various chemotherapeutic agents. Gene Set Enrichment Analysis (GSEA) was used to explore the potential mechanisms involved. Finally, Kaplan-Meier survival analysis and stratified analysis by tumor stage and lymph node status were performed to assess the prognostic value of the core gene. Results: WDR35 as a core gene associated with chemotherapy sensitivity and highly expressed in normal lung tissue compared with tumor tissue, which was further validated at both the qPCR and proteomic levels. Clinical correlation analysis indicated that WDR35 expression is significantly associated with tumor size, lymph node metastasis, and tumor stage. Further analysis revealed that patients with high WDR35 expression were more likely to achieve partial or complete response to initial chemotherapy. Drug sensitivity prediction analysis demonstrated that high WDR35 expression was significantly correlated with increased sensitivity to various anticancer drugs. GSEA pathway enrichment analysis suggested that WDR35 may enhance chemotherapy sensitivity by regulating stress response and metabolic pathways. Survival analysis indicated that high WDR35 expression was associated with better overall survival and disease-specific survival. Conclusions: Our study reveals that WDR35 is closely associated with chemotherapy sensitivity and prognosis in lung adenocarcinoma.

WDR35与肺腺癌化疗敏感性和预后相关
背景:本研究旨在探讨WD重复结构域35 (WDR35)在肺腺癌(LUAD)中的表达特征及其与化疗敏感性和预后的关系。方法:结合随机森林和支持向量机算法对差异表达基因进行分析,识别与化疗敏感性相关的关键基因。核心基因在转录组学和蛋白质组学水平上的表达差异,然后使用真实世界的LUAD样品进行实验验证。使用Genomics of Drug sensitivity in Cancer数据库进行药物敏感性分析,评估核心基因与各种化疗药物IC50值的相关性。基因集富集分析(GSEA)用于探讨可能的机制。最后,通过Kaplan-Meier生存分析和肿瘤分期及淋巴结状态分层分析来评估核心基因的预后价值。结果:与肿瘤组织相比,WDR35是与化疗敏感性相关的核心基因,在正常肺组织中高表达,进一步在qPCR和蛋白组学水平上得到验证。临床相关分析显示,WDR35表达与肿瘤大小、淋巴结转移及肿瘤分期有显著相关性。进一步分析显示,WDR35高表达的患者更有可能对初始化疗实现部分或完全缓解。药物敏感性预测分析表明,WDR35高表达与对多种抗癌药物的敏感性增加显著相关。GSEA通路富集分析提示WDR35可能通过调节应激反应和代谢途径增强化疗敏感性。生存分析表明,WDR35高表达与更好的总生存和疾病特异性生存相关。结论:我们的研究表明,WDR35与肺腺癌的化疗敏感性和预后密切相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
7.80
自引率
2.90%
发文量
87
审稿时长
3 months
期刊介绍: Cancer Biotherapy and Radiopharmaceuticals is the established peer-reviewed journal, with over 25 years of cutting-edge content on innovative therapeutic investigations to ultimately improve cancer management. It is the only journal with the specific focus of cancer biotherapy and is inclusive of monoclonal antibodies, cytokine therapy, cancer gene therapy, cell-based therapies, and other forms of immunotherapies. The Journal includes extensive reporting on advancements in radioimmunotherapy, and the use of radiopharmaceuticals and radiolabeled peptides for the development of new cancer treatments.
×
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