Enhancer RNA from STAT3 locus affects temozolomide chemoresistance of glioblastoma cells.

IF 2.6 3区 生物学 Q2 GENETICS & HEREDITY
Gene Pub Date : 2025-01-30 DOI:10.1016/j.gene.2025.149297
Ekaterina Mikhailovna Stasevich, Anastasiia Vladimirovna Simonova, Anastasiya Valeryevna Poteryakhina, Elvina Andreevna Bogomolova, Aksinya Nikolaevna Uvarova, Elina Alekseevna Zheremyan, Kirill Viktorovich Korneev, Anton Markovich Schwartz, Dmitry Vladimirovich Kuprash, Denis Eriksonovich Demin
{"title":"Enhancer RNA from STAT3 locus affects temozolomide chemoresistance of glioblastoma cells.","authors":"Ekaterina Mikhailovna Stasevich, Anastasiia Vladimirovna Simonova, Anastasiya Valeryevna Poteryakhina, Elvina Andreevna Bogomolova, Aksinya Nikolaevna Uvarova, Elina Alekseevna Zheremyan, Kirill Viktorovich Korneev, Anton Markovich Schwartz, Dmitry Vladimirovich Kuprash, Denis Eriksonovich Demin","doi":"10.1016/j.gene.2025.149297","DOIUrl":null,"url":null,"abstract":"<p><p>Less than ten percent of glioblastoma tumors are sensitive to temozolomide, the primary drug for treating this type of cancer. STAT3 is a well-known regulator of glioblastoma resistance to temozolomide, suppression of its activity sensitizes cells to the treatment. However, systemic suppression of STAT3 may lead to immune dysregulation, possibly interfering with the antitumor effect. Non-coding RNAs expressed from enhancers (enhancer RNA or eRNA) can guide the direction of various cellular processes by controlling the expression of key genes. In this work, we found eRNA from the STAT3 locus (TMZR1-eRNA) that controls the sensitivity of glioblastoma cells to temozolomide. Knockdown of TMZR1-eRNA decreased STAT3 mRNA and protein expression, resulting in a profound reduction in the abundance of temozolomide-treated cells. Using the reporter assay, we showed that eRNA suppression reduced the activity of STAT3 promoter. Patient glioblastoma cells with higher eRNA expression also showed enhanced sensitivity to temozolomide upon eRNA knockdown. Expression of the eRNA in healthy brain tissue and PBMC was observed at markedly lower levels. Taken together, our results suggest TMZR1-eRNA suppression as a more targeted approach to STAT3 inhibition, potentially with minimal side effects.</p>","PeriodicalId":12499,"journal":{"name":"Gene","volume":" ","pages":"149297"},"PeriodicalIF":2.6000,"publicationDate":"2025-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gene","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.gene.2025.149297","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

Less than ten percent of glioblastoma tumors are sensitive to temozolomide, the primary drug for treating this type of cancer. STAT3 is a well-known regulator of glioblastoma resistance to temozolomide, suppression of its activity sensitizes cells to the treatment. However, systemic suppression of STAT3 may lead to immune dysregulation, possibly interfering with the antitumor effect. Non-coding RNAs expressed from enhancers (enhancer RNA or eRNA) can guide the direction of various cellular processes by controlling the expression of key genes. In this work, we found eRNA from the STAT3 locus (TMZR1-eRNA) that controls the sensitivity of glioblastoma cells to temozolomide. Knockdown of TMZR1-eRNA decreased STAT3 mRNA and protein expression, resulting in a profound reduction in the abundance of temozolomide-treated cells. Using the reporter assay, we showed that eRNA suppression reduced the activity of STAT3 promoter. Patient glioblastoma cells with higher eRNA expression also showed enhanced sensitivity to temozolomide upon eRNA knockdown. Expression of the eRNA in healthy brain tissue and PBMC was observed at markedly lower levels. Taken together, our results suggest TMZR1-eRNA suppression as a more targeted approach to STAT3 inhibition, potentially with minimal side effects.

求助全文
约1分钟内获得全文 求助全文
来源期刊
Gene
Gene 生物-遗传学
CiteScore
6.10
自引率
2.90%
发文量
718
审稿时长
42 days
期刊介绍: Gene publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses.
×
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:481959085
Book学术官方微信