Study of NALT1 and CTBP1-AS1 lncRNAs expression levels in triple-negative breast cancer patients in the Iranian population

IF 1 Q4 GENETICS & HEREDITY Gene Reports Pub Date : 2024-09-01 DOI:10.1016/j.genrep.2024.102021
Elham Aminirad , Tala Haghnazari-Esfahlan , Ali Rajabi, Elaheh Hassannezhad-Daneshmand, Reza Safaralizadeh
{"title":"Study of NALT1 and CTBP1-AS1 lncRNAs expression levels in triple-negative breast cancer patients in the Iranian population","authors":"Elham Aminirad ,&nbsp;Tala Haghnazari-Esfahlan ,&nbsp;Ali Rajabi,&nbsp;Elaheh Hassannezhad-Daneshmand,&nbsp;Reza Safaralizadeh","doi":"10.1016/j.genrep.2024.102021","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Triple-negative breast cancer (TNBC), an aggressive subtype with a poor prognosis, is notably difficult to treat. Emerging research highlights the significant roles of long non-coding RNAs (lncRNAs) in cancer biology. LncRNAs, such as <em>NALT1</em> and <em>CTBP1-AS1</em> are implicated in oncogenic processes; this study hypothesizes that <em>NALT1</em> and <em>CTBP1-AS1</em> are overexpressed in TNBC tissues compared to adjacent non-tumor tissues and may serve as biomarkers. Methods: One hundred pairs of tumor and adjacent non-tumor tissues were obtained from female patients with triple-negative breast cancer. After extracting RNA, cDNA synthesis was carried out for all samples. Quantitative real-time PCR (qRT-PCR) was employed to assess differential gene expression. Results: The expression of <em>NALT1</em> (<em>p</em>-value &lt;0.0001) and <em>CTBP1-AS1</em> (p-value &lt;0.0002) lncRNAs increased in TNBC tumor tissues in comparison to adjacent non-tumor tissues. A statistically positive correlation (ρ = 0.5844, <em>p</em> &lt; 0.0001) was observed between the expression levels of <em>NALT1</em> and <em>CTBP1-AS1</em> in breast cancer patients. The ROC analysis indicated that <em>NALT1</em> (AUC = 0.718, specificity = 61 %, sensitivity = 70 %) shows moderate potential and <em>CTBP1-AS1</em> (AUC = 0.648, specificity = 65 %, sensitivity = 55 %) exhibits poor potential as a diagnostic biomarker for breast cancer. Conclusion: This study shows that <em>NALT1</em> and <em>CTBP1-AS1</em> lncRNAs are upregulated in TNBC tissues. Additionally, a positive correlation exists between their expression levels in breast cancer. Further research is needed to understand their mechanisms as molecular biomarkers.</p></div>","PeriodicalId":12673,"journal":{"name":"Gene Reports","volume":"37 ","pages":"Article 102021"},"PeriodicalIF":1.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gene Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2452014424001444","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Triple-negative breast cancer (TNBC), an aggressive subtype with a poor prognosis, is notably difficult to treat. Emerging research highlights the significant roles of long non-coding RNAs (lncRNAs) in cancer biology. LncRNAs, such as NALT1 and CTBP1-AS1 are implicated in oncogenic processes; this study hypothesizes that NALT1 and CTBP1-AS1 are overexpressed in TNBC tissues compared to adjacent non-tumor tissues and may serve as biomarkers. Methods: One hundred pairs of tumor and adjacent non-tumor tissues were obtained from female patients with triple-negative breast cancer. After extracting RNA, cDNA synthesis was carried out for all samples. Quantitative real-time PCR (qRT-PCR) was employed to assess differential gene expression. Results: The expression of NALT1 (p-value <0.0001) and CTBP1-AS1 (p-value <0.0002) lncRNAs increased in TNBC tumor tissues in comparison to adjacent non-tumor tissues. A statistically positive correlation (ρ = 0.5844, p < 0.0001) was observed between the expression levels of NALT1 and CTBP1-AS1 in breast cancer patients. The ROC analysis indicated that NALT1 (AUC = 0.718, specificity = 61 %, sensitivity = 70 %) shows moderate potential and CTBP1-AS1 (AUC = 0.648, specificity = 65 %, sensitivity = 55 %) exhibits poor potential as a diagnostic biomarker for breast cancer. Conclusion: This study shows that NALT1 and CTBP1-AS1 lncRNAs are upregulated in TNBC tissues. Additionally, a positive correlation exists between their expression levels in breast cancer. Further research is needed to understand their mechanisms as molecular biomarkers.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
伊朗三阴性乳腺癌患者中 NALT1 和 CTBP1-AS1 lncRNAs 表达水平的研究
背景三阴性乳腺癌(TNBC)是一种侵袭性亚型癌症,预后较差,尤其难以治疗。新近的研究强调了长非编码 RNA(lncRNA)在癌症生物学中的重要作用。NALT1和CTBP1-AS1等LncRNA与致癌过程有关;本研究推测,与邻近的非肿瘤组织相比,NALT1和CTBP1-AS1在TNBC组织中过表达,可作为生物标志物。研究方法从女性三阴性乳腺癌患者中获取 100 对肿瘤组织和邻近非肿瘤组织。提取 RNA 后,对所有样本进行 cDNA 合成。采用定量实时 PCR(qRT-PCR)技术评估不同基因的表达。结果显示与邻近的非肿瘤组织相比,NALT1(p-value <0.0001)和CTBP1-AS1(p-value <0.0002)lncRNA在TNBC肿瘤组织中的表达量增加。NALT1和CTBP1-AS1在乳腺癌患者中的表达水平呈统计学正相关(ρ = 0.5844, p <0.0001)。ROC分析表明,NALT1(AUC = 0.718,特异性 = 61 %,灵敏度 = 70 %)显示出中等潜力,而 CTBP1-AS1(AUC = 0.648,特异性 = 65 %,灵敏度 = 55 %)作为乳腺癌诊断生物标记物的潜力较差。结论本研究表明,NALT1 和 CTBP1-AS1 lncRNA 在 TNBC 组织中上调。此外,它们在乳腺癌中的表达水平呈正相关。要了解它们作为分子生物标志物的机制,还需要进一步的研究。
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 去求助
来源期刊
Gene Reports
Gene Reports Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍: Gene Reports 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. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.
期刊最新文献
Role of 1,25-dihydroxy vitamin D3 pathway in chronic urticaria: Findings from a hospital-based case-control study Exploitation of novel drought responsive EST-SSR markers in tetraploid cotton (Gossypium hirsutum L.) Investigating the Rrelationship between polymorphisms pd1.9 and rs7421861 of PD1 gene with breast cancer In-silico analysis of XRCC5 non-synonymous single nucleotide polymorphisms (nsSNPs) in acute myeloid leukemia prognosis Exome sequencing and molecular dynamics simulation characterizes a compound heterozygous GCDH missense variant leading to glutaric aciduria type 1 in a paediatric patient from Jammu and Kashmir, India
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1