[Application of Targeted mRNA Sequencing in Fusion Genes Diagnosis of Hematologic Diseases].

Q4 Medicine
Man Wang, Ling Zhang, Yan Chen, Jun-Dan Xie, Hong Yao, Li Yao, Jian-Nong Cen, Zi-Xing Chen, Su-Ning Chen, Hong-Jie Shen
{"title":"[Application of Targeted mRNA Sequencing in Fusion Genes Diagnosis of Hematologic Diseases].","authors":"Man Wang, Ling Zhang, Yan Chen, Jun-Dan Xie, Hong Yao, Li Yao, Jian-Nong Cen, Zi-Xing Chen, Su-Ning Chen, Hong-Jie Shen","doi":"10.19746/j.cnki.issn.1009-2137.2025.04.042","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To explore the application of targeted mRNA sequencing in fusion gene diagnosis of hematologic diseases.</p><p><strong>Methods: </strong>Bone marrow or peripheral blood samples of 105 patients with abnormally elevated eosinophil proportions and 291 acute leukemia patients from January 2015 to June 2023 in the First Affiliated Hospital of Soochow University were analyzed and gene structural variants were detected by targeted mRNA sequencing.</p><p><strong>Results: </strong>Among 105 patients with abnormally elevated eosinophil proportions, 6 cases were detected with gene structural variants, among which fusion gene testing results in 5 cases could serve as diagnostic indicators for myeloid neoplasms with eosinophilia. In addition, a <i>IL3</i>∷<i>ETV6</i> fusion gene was detected in one patient with chronic eosinophilic leukemia, not otherwise specified. Among 119 patients with acute myeloid leukemia (AML), 38 cases were detected structural variants by targeted mRNA sequencing, accounting for 31.9%, which was significantly higher than 20.2% (24/119) detected by multiple quantitative PCR (<i>P</i> < 0.05). We also found one patient with AML had both <i>NUP98</i>∷<i>PRRX2</i> and <i>KCTD5</i>∷<i>JAK2</i> fusion genes. A total of 104 patients were detected structural variants by targeted mRNA sequencing in 172 cases with acute B-lymphoblastic leukemia who were tested negative by multiple quantitative PCR, with a detection rate of 60.5% (102/172).</p><p><strong>Conclusion: </strong>Targeted mRNA sequencing can effectively detect fusion gene and has potential clinical application value in diagnosis and classificatation in hematologic diseases.</p>","PeriodicalId":35777,"journal":{"name":"中国实验血液学杂志","volume":"33 4","pages":"1209-1216"},"PeriodicalIF":0.0000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"中国实验血液学杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.19746/j.cnki.issn.1009-2137.2025.04.042","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: To explore the application of targeted mRNA sequencing in fusion gene diagnosis of hematologic diseases.

Methods: Bone marrow or peripheral blood samples of 105 patients with abnormally elevated eosinophil proportions and 291 acute leukemia patients from January 2015 to June 2023 in the First Affiliated Hospital of Soochow University were analyzed and gene structural variants were detected by targeted mRNA sequencing.

Results: Among 105 patients with abnormally elevated eosinophil proportions, 6 cases were detected with gene structural variants, among which fusion gene testing results in 5 cases could serve as diagnostic indicators for myeloid neoplasms with eosinophilia. In addition, a IL3ETV6 fusion gene was detected in one patient with chronic eosinophilic leukemia, not otherwise specified. Among 119 patients with acute myeloid leukemia (AML), 38 cases were detected structural variants by targeted mRNA sequencing, accounting for 31.9%, which was significantly higher than 20.2% (24/119) detected by multiple quantitative PCR (P < 0.05). We also found one patient with AML had both NUP98PRRX2 and KCTD5JAK2 fusion genes. A total of 104 patients were detected structural variants by targeted mRNA sequencing in 172 cases with acute B-lymphoblastic leukemia who were tested negative by multiple quantitative PCR, with a detection rate of 60.5% (102/172).

Conclusion: Targeted mRNA sequencing can effectively detect fusion gene and has potential clinical application value in diagnosis and classificatation in hematologic diseases.

[靶向mRNA测序在血液疾病融合基因诊断中的应用]。
目的:探讨靶向mRNA测序在血液病融合基因诊断中的应用。方法:分析2015年1月至2023年6月苏州大学第一附属医院嗜酸性粒细胞比例异常升高的105例患者和291例急性白血病患者的骨髓或外周血样本,通过靶向mRNA测序检测基因结构变异。结果:105例嗜酸性粒细胞比例异常升高的患者中,6例检测到基因结构变异,其中5例融合基因检测结果可作为嗜酸性粒细胞髓系肿瘤的诊断指标。此外,在一名慢性嗜酸性白血病患者中检测到IL3∷ETV6融合基因,没有其他说明。119例急性髓性白血病(AML)患者中,靶向mRNA测序检测到结构变异38例,占31.9%,显著高于多次定量PCR检测到的20.2% (24/119)(P < 0.05)。我们还发现一名AML患者同时具有NUP98∷PRRX2和KCTD5∷JAK2融合基因。172例急性b淋巴细胞白血病患者经多重定量PCR检测为阴性,通过靶向mRNA测序共检测出104例结构变异,检出率为60.5%(102/172)。结论:靶向mRNA测序可有效检测融合基因,在血液病的诊断和分型中具有潜在的临床应用价值。
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
中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
7331
期刊介绍:
×
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