Comparative analysis of RNA expression identifies effective targeted drug in myoepithelial carcinoma.

IF 6.8 1区 医学 Q1 ONCOLOGY
Yvonne A Vasquez, Lauren Sanders, Holly C Beale, A Geoffrey Lyle, Ellen T Kephart, Katrina Learned, Jennifer Peralez, Amy Li, Min Huang, Kimberly A Pyke-Grimm, Serena Y Tan, Sofie R Salama, David Haussler, Isabel Bjork, Olena M Vaske, Sheri L Spunt
{"title":"Comparative analysis of RNA expression identifies effective targeted drug in myoepithelial carcinoma.","authors":"Yvonne A Vasquez, Lauren Sanders, Holly C Beale, A Geoffrey Lyle, Ellen T Kephart, Katrina Learned, Jennifer Peralez, Amy Li, Min Huang, Kimberly A Pyke-Grimm, Serena Y Tan, Sofie R Salama, David Haussler, Isabel Bjork, Olena M Vaske, Sheri L Spunt","doi":"10.1038/s41698-025-00918-5","DOIUrl":null,"url":null,"abstract":"<p><p>Myoepithelial carcinoma is an ultra-rare pediatric solid tumor with no targeted treatments. Clinical implementation of tumor RNA sequencing (RNA-Seq) for identifying therapeutic targets is underexplored in pediatric cancer. We previously published the Comparative Analysis of RNA Expression (CARE), a framework for incorporating RNA-Seq-derived gene expression into the clinic for difficult-to-treat pediatric cancers. Here, we discuss a 4-year-old male diagnosed with myoepithelial carcinoma who was treated at Stanford Medicine Children's Health. A metastatic lung nodule from the patient underwent standard-of-care tumor DNA profiling and CARE analysis, wherein the patient's tumor RNA-Seq profile was compared to over 11,000 uniformly analyzed tumor profiles from public data repositories. DNA profiling yielded no actionable mutations. CARE identified overexpression biomarkers and nominated a treatment that produced a durable clinical response. These findings underscore the utility of data sharing and concurrent analysis of large genomic datasets for clinical benefit, particularly for rare cancers with unknown biological drivers.</p>","PeriodicalId":19433,"journal":{"name":"NPJ Precision Oncology","volume":"9 1","pages":"145"},"PeriodicalIF":6.8000,"publicationDate":"2025-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12084418/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NPJ Precision Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41698-025-00918-5","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Myoepithelial carcinoma is an ultra-rare pediatric solid tumor with no targeted treatments. Clinical implementation of tumor RNA sequencing (RNA-Seq) for identifying therapeutic targets is underexplored in pediatric cancer. We previously published the Comparative Analysis of RNA Expression (CARE), a framework for incorporating RNA-Seq-derived gene expression into the clinic for difficult-to-treat pediatric cancers. Here, we discuss a 4-year-old male diagnosed with myoepithelial carcinoma who was treated at Stanford Medicine Children's Health. A metastatic lung nodule from the patient underwent standard-of-care tumor DNA profiling and CARE analysis, wherein the patient's tumor RNA-Seq profile was compared to over 11,000 uniformly analyzed tumor profiles from public data repositories. DNA profiling yielded no actionable mutations. CARE identified overexpression biomarkers and nominated a treatment that produced a durable clinical response. These findings underscore the utility of data sharing and concurrent analysis of large genomic datasets for clinical benefit, particularly for rare cancers with unknown biological drivers.

RNA表达对比分析确定肌上皮癌有效靶向药物。
肌上皮癌是一种非常罕见的儿童实体肿瘤,没有靶向治疗。临床实施肿瘤RNA测序(RNA- seq)确定治疗靶点在儿科癌症尚未充分探索。我们之前发表了RNA表达的比较分析(CARE),这是一个将RNA- seq衍生的基因表达纳入临床治疗难以治疗的儿科癌症的框架。在这里,我们讨论一个4岁的男性诊断为肌上皮癌谁是在斯坦福医学儿童健康治疗。来自患者的转移性肺结节接受了标准治疗的肿瘤DNA分析和CARE分析,其中患者的肿瘤RNA-Seq谱与来自公共数据库的11,000多个统一分析的肿瘤谱进行了比较。DNA分析没有发现可操作的突变。CARE确定了过表达的生物标志物,并提名了一种产生持久临床反应的治疗方法。这些发现强调了数据共享和大型基因组数据集并发分析对临床益处的效用,特别是对具有未知生物学驱动因素的罕见癌症。
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
9.90
自引率
1.30%
发文量
87
审稿时长
18 weeks
期刊介绍: Online-only and open access, npj Precision Oncology is an international, peer-reviewed journal dedicated to showcasing cutting-edge scientific research in all facets of precision oncology, spanning from fundamental science to translational applications and clinical medicine.
×
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