• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

长链非编码RNA HEIH在急性髓系白血病患者中的表达及临床意义

[Expression and Clinical Significance of LncRNA HEIH in Patients with Acute Myeloid Leukemia].

作者信息

Ma Yue, Li Jia-Jia

机构信息

Department of Hematology, The First Affiliated Hospital of Bengbu Medical College, Bengbu 233000, Anhui Province, China.

Department of Hematology, The First Affiliated Hospital of Bengbu Medical College, Bengbu 233000, Anhui Province, China. E-mail:

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2024 Aug;32(4):1011-1017. doi: 10.19746/j.cnki.issn.1009-2137.2024.04.006.

DOI:10.19746/j.cnki.issn.1009-2137.2024.04.006
PMID:39192391
Abstract

OBJECTIVE

To investigate the expression and clinical significance of long noncoding RNA(lncRNA) HEIH in patients with acute myeloid leukemia (AML).

METHODS

50 newly diagnosed AML patients (except M3) admitted to the First Affiliated Hospital of Bengbu Medical College from January 2019 to December 2020 were included in the study, with 30 patients with non-hematological malignancies as controls. The relative expression level of lncRNA HEIH in all patients were detected, the correlation of clinical characteristics, gene mutations, FAB classification, efficacy, prognosis and overall survival (OS) of AML patients with the expression level of lncRNA HEIH were analyzed.

RESULTS

The expression level of lncRNA HEIH in AML patients was significantly higher than that in patients with non-hematological malignancies ( <0.01). Moreover, AML patients with high white blood cell count (WBC), and mutations, poor efficacy, and poor prognosis often showed higher expression of lncRNA HEIH, and patients with high lncRNA HEIH expression showed a shorter overall survival (OS).

CONCLUSION

lncRNA HEIH shows an unique molecular biological significance in AML patients, which may provide a new approach for diagnosis, monitoring and targeted therapy of AML.

摘要

目的

探讨长链非编码RNA(lncRNA)HEIH在急性髓系白血病(AML)患者中的表达及临床意义。

方法

纳入2019年1月至2020年12月蚌埠医学院第一附属医院收治的50例新诊断AML患者(M3除外),以30例非血液系统恶性肿瘤患者作为对照。检测所有患者lncRNA HEIH的相对表达水平,分析AML患者lncRNA HEIH表达水平与临床特征、基因突变、FAB分型、疗效、预后及总生存期(OS)的相关性。

结果

AML患者lncRNA HEIH表达水平显著高于非血液系统恶性肿瘤患者(<0.01)。此外,白细胞计数(WBC)高、有 突变、疗效差及预后差的AML患者lncRNA HEIH表达往往较高,lncRNA HEIH高表达患者的总生存期(OS)较短。

结论

lncRNA HEIH在AML患者中具有独特的分子生物学意义,可能为AML的诊断、监测及靶向治疗提供新途径。

相似文献

1
[Expression and Clinical Significance of LncRNA HEIH in Patients with Acute Myeloid Leukemia].长链非编码RNA HEIH在急性髓系白血病患者中的表达及临床意义
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2024 Aug;32(4):1011-1017. doi: 10.19746/j.cnki.issn.1009-2137.2024.04.006.
2
[Clinical features and prognostic factors in adult acute myeloid leukemia patients with FLT3-ITD and CEBPA gene co-mutation].[伴有FLT3-ITD和CEBPA基因共突变的成人急性髓系白血病患者的临床特征及预后因素]
Zhonghua Xue Ye Xue Za Zhi. 2020 Apr 14;41(4):297-301. doi: 10.3760/cma.j.issn.0253-2727.2020.04.007.
3
Clinical significance of FLT3-ITD/CEBPA mutations and minimal residual disease in cytogenetically normal acute myeloid leukemia after hematopoietic stem cell transplantation.FLT3-ITD/CEBPA 基因突变和细胞遗传学正常的急性髓细胞白血病造血干细胞移植后微小残留病的临床意义。
J Cancer Res Clin Oncol. 2021 Sep;147(9):2659-2670. doi: 10.1007/s00432-021-03530-9. Epub 2021 Feb 7.
4
Double CEBPA mutations are prognostically favorable in non-M3 acute myeloid leukemia patients with wild-type NPM1 and FLT3-ITD.在具有野生型NPM1和FLT3-ITD的非M3急性髓系白血病患者中,双CEBPA突变预后良好。
Int J Clin Exp Pathol. 2014 Sep 15;7(10):6832-40. eCollection 2014.
5
[Expression of lncRNA UCA1 in Acute Myeloid Leukemia Patients and Its Clinical Significance].[长链非编码RNA UCA1在急性髓系白血病患者中的表达及其临床意义]
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2024 Aug;32(4):999-1004. doi: 10.19746/j.cnki.issn.1009-2137.2024.04.004.
6
Prognostic significance of, and gene and microRNA expression signatures associated with, CEBPA mutations in cytogenetically normal acute myeloid leukemia with high-risk molecular features: a Cancer and Leukemia Group B Study.具有高危分子特征的细胞遗传学正常的急性髓系白血病中CEBPA突变的预后意义以及与之相关的基因和微小RNA表达特征:癌症与白血病B组研究
J Clin Oncol. 2008 Nov 1;26(31):5078-87. doi: 10.1200/JCO.2008.17.5554. Epub 2008 Sep 22.
7
The effect of the detection of minimal residual disease for the prognosis and the choice of post-remission therapy of intermediate-risk acute myeloid leukemia without FLT3-ITD, NPM1 and biallelic CEBPA mutations.无 FLT3-ITD、NPM1 和双等位 CEBPA 突变的中危急性髓系白血病微小残留病检测对预后和缓解后治疗选择的影响。
Hematology. 2021 Dec;26(1):179-185. doi: 10.1080/16078454.2021.1880753.
8
[Gene Profile and Clinical Significance of Concomitant Mutations in CN-AML Patients with Mutation].[伴有突变的CN-AML患者中伴随突变的基因谱及临床意义]
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2024 Apr;32(2):335-341. doi: 10.19746/j.cnki.issn.1009-2137.2024.02.002.
9
Prognostic significance of FLT3 internal tandem duplication, nucleophosmin 1, and CEBPA gene mutations for acute myeloid leukemia patients with normal karyotype and younger than 60 years: a systematic review and meta-analysis.核磷酸蛋白 1、CEBPA 基因突变和 FLT3 内部串联重复对核型正常且年龄小于 60 岁的急性髓系白血病患者的预后意义:系统评价和荟萃分析。
Ann Hematol. 2014 Aug;93(8):1279-86. doi: 10.1007/s00277-014-2072-6. Epub 2014 May 7.
10
[NPM1 and CEBPA mutations in pediatric cytogenetically normal acute myeloid leukemia].儿童细胞遗传学正常的急性髓系白血病中的NPM1和CEBPA突变
Zhonghua Er Ke Za Zhi. 2014 Apr;52(4):303-7.

引用本文的文献

1
Systematic review and meta-analysis of the impact of abnormal expression of long non coding RNA on the prognosis of acute myeloid leukemia.长链非编码RNA异常表达对急性髓系白血病预后影响的系统评价和Meta分析
Front Genet. 2025 Feb 4;16:1524449. doi: 10.3389/fgene.2025.1524449. eCollection 2025.