Destabilization of hsa_circ_0015508 by YTHDF2 Enhances miR-496-Mediated FOXN3 Suppression to Drive Nasopharyngeal Carcinoma Progression.

IF 4.6 4区 医学 Q3 ONCOLOGY
Oncology Research Pub Date : 2026-09-14 eCollection Date: 2026-01-01 DOI:10.32604/or.2026.084662
Aiyu Ma, Xu Wang, Lu Lu, Shuaijie Wang, Qiuyu Zhao, Xuemei Zhang, Yiping Sun, Xuan Meng, Yan Zhang, Yuzhong Yang, Jinhua Zheng, Xiang Zheng
{"title":"Destabilization of hsa_circ_0015508 by YTHDF2 Enhances miR-496-Mediated FOXN3 Suppression to Drive Nasopharyngeal Carcinoma Progression.","authors":"Aiyu Ma, Xu Wang, Lu Lu, Shuaijie Wang, Qiuyu Zhao, Xuemei Zhang, Yiping Sun, Xuan Meng, Yan Zhang, Yuzhong Yang, Jinhua Zheng, Xiang Zheng","doi":"10.32604/or.2026.084662","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objectives:</b> YTH N6-Methyladenosine RNA Binding Protein F2 (YTHDF2) had been implicated in nasopharyngeal carcinoma (NPC) progression. Increasing evidence indicated that numerous circular RNAs (circRNAs) were involved in regulating tumor progression. However, how the regulation of circRNAs by YTHDF2 contributes to NPC progression remains to be uncovered. In this study, we aimed to elucidate the role and mechanism of YTHDF2-mediated circRNA regulation in NPC migration and invasion. <b>Methods:</b> YTHDF2 expression in NPC was assessed using GEO datasets and immunohistochemistry. Functional experiments were performed in HNE1 and 5-8F cells, with migration/invasion evaluated by wound healing and transwell assays, and epithelial-mesenchymal transition (EMT) markers by Western blotting. CircRNA candidates were screened through circRNA sequencing. CircRNA m6A modification was assessed by methylated RNA immunoprecipitation-quantitative PCR (MeRIP-qPCR). The SELECT method (single-base elongation- and ligation-based qPCR amplification) was used to identify the specific m6A modification site. RNA stability was measured by actinomycin D assay. circRNA-miRNA and miRNA-target interactions were validated by luciferase reporter assays. <b>Results:</b> YTHDF2 expression was upregulated in NPC tissues and was found to promote <i>in vitro</i> migration and invasion phenotypes. Mechanistically, m6A-modified <i>circ_0015508</i> was recognized and degraded by YTHDF2. YTHDF2-mediated pro-migration and pro-invasion effects were reversed by <i>circ_0015508</i>. <i>FOXN3</i> was identified as a target of <i>miR-496</i>. <i>Circ_0015508</i> was found to sequester <i>miR-496</i>, thereby de-repressing <i>FOXN3</i> expression. <b>Conclusion:</b> In this study, a potential oncogenic pathway was delineated in which NPC migration and invasion were facilitated by YTHDF2 via degradation of <i>circ_0015508</i>, thereby the sponging effect of <i>miR-496</i> was abolished and <i>FOXN3</i> expression was suppressed.</p>","PeriodicalId":19537,"journal":{"name":"Oncology Research","volume":"34 10","pages":"26"},"PeriodicalIF":4.6000,"publicationDate":"2026-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13591364/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oncology Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.32604/or.2026.084662","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: YTH N6-Methyladenosine RNA Binding Protein F2 (YTHDF2) had been implicated in nasopharyngeal carcinoma (NPC) progression. Increasing evidence indicated that numerous circular RNAs (circRNAs) were involved in regulating tumor progression. However, how the regulation of circRNAs by YTHDF2 contributes to NPC progression remains to be uncovered. In this study, we aimed to elucidate the role and mechanism of YTHDF2-mediated circRNA regulation in NPC migration and invasion. Methods: YTHDF2 expression in NPC was assessed using GEO datasets and immunohistochemistry. Functional experiments were performed in HNE1 and 5-8F cells, with migration/invasion evaluated by wound healing and transwell assays, and epithelial-mesenchymal transition (EMT) markers by Western blotting. CircRNA candidates were screened through circRNA sequencing. CircRNA m6A modification was assessed by methylated RNA immunoprecipitation-quantitative PCR (MeRIP-qPCR). The SELECT method (single-base elongation- and ligation-based qPCR amplification) was used to identify the specific m6A modification site. RNA stability was measured by actinomycin D assay. circRNA-miRNA and miRNA-target interactions were validated by luciferase reporter assays. Results: YTHDF2 expression was upregulated in NPC tissues and was found to promote in vitro migration and invasion phenotypes. Mechanistically, m6A-modified circ_0015508 was recognized and degraded by YTHDF2. YTHDF2-mediated pro-migration and pro-invasion effects were reversed by circ_0015508. FOXN3 was identified as a target of miR-496. Circ_0015508 was found to sequester miR-496, thereby de-repressing FOXN3 expression. Conclusion: In this study, a potential oncogenic pathway was delineated in which NPC migration and invasion were facilitated by YTHDF2 via degradation of circ_0015508, thereby the sponging effect of miR-496 was abolished and FOXN3 expression was suppressed.

YTHDF2破坏hsa_circ_0015508的稳定性,增强mir -496介导的FOXN3抑制,驱动鼻咽癌进展
目的:ythn6 -甲基腺苷RNA结合蛋白F2 (YTHDF2)与鼻咽癌(NPC)进展有关。越来越多的证据表明,许多环状rna (circRNAs)参与调节肿瘤进展。然而,YTHDF2对circrna的调控如何促进NPC进展仍有待发现。在本研究中,我们旨在阐明ythdf2介导的circRNA调控在NPC迁移和侵袭中的作用和机制。方法:采用GEO数据集和免疫组织化学方法检测鼻咽癌组织中YTHDF2的表达。在HNE1和5-8F细胞中进行功能实验,通过伤口愈合和transwell实验评估迁移/侵袭,并通过Western blotting评估上皮-间充质转化(EMT)标记。通过CircRNA测序筛选候选CircRNA。通过甲基化RNA免疫沉淀定量PCR (MeRIP-qPCR)评估CircRNA m6A修饰。采用SELECT方法(单碱基延伸和基于连接的qPCR扩增)鉴定特异性m6A修饰位点。采用放线菌素D法测定RNA稳定性。荧光素酶报告基因检测证实了circRNA-miRNA和mirna -靶标相互作用。结果:YTHDF2在鼻咽癌组织中表达上调,并促进体外迁移和侵袭表型。在机制上,m6a修饰的circ_0015508被YTHDF2识别并降解。ythdf2介导的促迁移和促侵袭作用被circ_0015508逆转。FOXN3被确定为miR-496的靶标。Circ_0015508被发现隔离miR-496,从而去抑制FOXN3的表达。结论:本研究描绘了一条潜在的致癌途径,YTHDF2通过降解circ_0015508促进鼻咽癌的迁移和侵袭,从而消除miR-496的海绵作用,抑制FOXN3的表达。
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
Oncology Research
Oncology Research 医学-肿瘤学
CiteScore
4.40
自引率
0.00%
发文量
56
审稿时长
3 months
期刊介绍: Oncology Research Featuring Preclinical and Clincal Cancer Therapeutics publishes research of the highest quality that contributes to an understanding of cancer in areas of molecular biology, cell biology, biochemistry, biophysics, genetics, biology, endocrinology, and immunology, as well as studies on the mechanism of action of carcinogens and therapeutic agents, reports dealing with cancer prevention and epidemiology, and clinical trials delineating effective new therapeutic regimens.
×
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