• 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

基因表达特征可预测细胞遗传学正常的成人急性髓系白血病患者的复发。

Gene expression signature predicts relapse in adult patients with cytogenetically normal acute myeloid leukemia.

机构信息

The Ohio State University Comprehensive Cancer Center, Columbus OH.

Alliance Statistics and Data Center, The Ohio State University Comprehensive Cancer Center, Columbus, OH.

出版信息

Blood Adv. 2021 Mar 9;5(5):1474-1482. doi: 10.1182/bloodadvances.2020003727.

DOI:10.1182/bloodadvances.2020003727
PMID:33683341
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7948288/
Abstract

Although ∼80% of adult patients with cytogenetically normal acute myeloid leukemia (CN-AML) achieve a complete remission (CR), more than half of them relapse. Better identification of patients who are likely to relapse can help to inform clinical decisions. We performed RNA sequencing on pretreatment samples from 268 adults with de novo CN-AML who were younger than 60 years of age and achieved a CR after induction treatment with standard "7+3" chemotherapy. After filtering for genes whose expressions were associated with gene mutations known to impact outcome (ie, CEBPA, NPM1, and FLT3-internal tandem duplication [FLT3-ITD]), we identified a 10-gene signature that was strongly predictive of patient relapse (area under the receiver operating characteristics curve [AUC], 0.81). The signature consisted of 7 coding genes (GAS6, PSD3, PLCB4, DEXI, JMY, NRP1, C10orf55) and 3 long noncoding RNAs. In multivariable analysis, the 10-gene signature was strongly associated with relapse (P < .001), after adjustment for the FLT3-ITD, CEBPA, and NPM1 mutational status. Validation of the expression signature in an independent patient set from The Cancer Genome Atlas showed the signature's strong predictive value, with AUC = 0.78. Implementation of the 10-gene signature into clinical prognostic stratification could be useful for identifying patients who are likely to relapse.

摘要

尽管有 ∼80% 的细胞遗传学正常的急性髓系白血病(CN-AML)成年患者达到完全缓解(CR),但其中超过一半的患者会复发。更好地识别可能复发的患者有助于指导临床决策。我们对 268 名年龄小于 60 岁且在诱导治疗后用标准的“7+3”化疗达到 CR 的初治 CN-AML 成年患者的预处理样本进行了 RNA 测序。在筛选与已知影响预后的基因突变(即 CEBPA、NPM1 和 FLT3 内部串联重复 [FLT3-ITD])相关的基因表达后,我们确定了一个强烈预测患者复发的 10 基因特征(接受者操作特征曲线下面积 [AUC],0.81)。该特征由 7 个编码基因(GAS6、PSD3、PLCB4、DEXI、JMY、NRP1、C10orf55)和 3 个长非编码 RNA 组成。在多变量分析中,10 基因特征与复发强烈相关(P<0.001),在调整了 FLT3-ITD、CEBPA 和 NPM1 突变状态后。在癌症基因组图谱中的另一个独立患者组中验证该表达特征显示出该特征具有很强的预测价值,AUC=0.78。将 10 基因特征纳入临床预后分层可能有助于识别可能复发的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f851/7948288/e1b7a15f8903/advancesADV2020003727absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f851/7948288/e1b7a15f8903/advancesADV2020003727absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f851/7948288/e1b7a15f8903/advancesADV2020003727absf1.jpg

相似文献

1
Gene expression signature predicts relapse in adult patients with cytogenetically normal acute myeloid leukemia.基因表达特征可预测细胞遗传学正常的成人急性髓系白血病患者的复发。
Blood Adv. 2021 Mar 9;5(5):1474-1482. doi: 10.1182/bloodadvances.2020003727.
2
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.
3
The prognostic impact of FLT3-ITD, NPM1 and CEBPa in cytogenetically intermediate-risk AML after first relapse.首次复发后,FLT3-ITD、NPM1 和 CEBPa 在细胞遗传学中危 AML 中的预后影响。
Int J Hematol. 2020 Aug;112(2):200-209. doi: 10.1007/s12185-020-02894-x. Epub 2020 Jun 3.
4
Prognostic implications of NPM1 mutations and FLT3 internal tandem duplications in Egyptian patients with cytogenetically normal acute myeloid leukemia.NPM1突变和FLT3内部串联重复在埃及细胞遗传学正常的急性髓系白血病患者中的预后意义
Hematology. 2014 Jan;19(1):22-30. doi: 10.1179/1607845413Y.0000000085. Epub 2013 Nov 25.
5
Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia.细胞遗传学正常的急性髓系白血病中的突变与治疗结果
N Engl J Med. 2008 May 1;358(18):1909-18. doi: 10.1056/NEJMoa074306.
6
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.
7
Expression of CD4 is correlated with an unfavorable prognosis in wild-type NPM1, FLT3-ITD-negative cytogenetically normal adult acute myeloid leukemia.在野生型核仁磷酸蛋白1(NPM1)、FMS样酪氨酸激酶3内部串联重复序列(FLT3-ITD)阴性、细胞遗传学正常的成年急性髓系白血病中,CD4的表达与不良预后相关。
Int J Lab Hematol. 2017 Aug;39(4):429-437. doi: 10.1111/ijlh.12649. Epub 2017 Mar 20.
8
Long non-coding RNA expression profile in cytogenetically normal acute myeloid leukemia identifies a distinct signature and a new biomarker in NPM1-mutated patients.在细胞遗传学正常的急性髓系白血病中长非编码 RNA 的表达谱鉴定了 NPM1 突变患者中的一个独特特征和一个新的生物标志物。
Haematologica. 2017 Oct;102(10):1718-1726. doi: 10.3324/haematol.2017.171645. Epub 2017 Jul 4.
9
Single nucleotide polymorphism in the mutational hotspot of WT1 predicts a favorable outcome in patients with cytogenetically normal acute myeloid leukemia.WT1 突变热点的单核苷酸多态性可预测细胞遗传学正常的急性髓系白血病患者的良好预后。
J Clin Oncol. 2010 Feb 1;28(4):578-85. doi: 10.1200/JCO.2009.23.0342. Epub 2009 Dec 28.
10
Identification of emerging FLT3 ITD-positive clones during clinical remission and kinetics of disease relapse in acute myeloid leukaemia with mutated nucleophosmin.核磷蛋白突变的急性髓系白血病临床缓解期出现的 FLT3 ITD 阳性克隆的鉴定及疾病复发的动力学研究
Br J Haematol. 2013 May;161(4):533-40. doi: 10.1111/bjh.12288. Epub 2013 Mar 11.

引用本文的文献

1
CCAAT-enhancer binding protein delta functions as a tumor suppressor gene in acute myeloid leukemia.CCAAT增强子结合蛋白δ在急性髓系白血病中作为一种肿瘤抑制基因发挥作用。
bioRxiv. 2025 Aug 27:2025.08.25.670309. doi: 10.1101/2025.08.25.670309.
2
Identification of a distinctive immunogenomic gene signature in stage-matched colorectal cancer.在分期匹配的结直肠癌中鉴定独特的免疫基因组基因特征
J Cancer Res Clin Oncol. 2024 Dec 14;151(1):9. doi: 10.1007/s00432-024-06034-4.
3
The co-receptor Neuropilin-1 enhances proliferation in inv(16) acute myeloid leukemia via VEGF signaling.

本文引用的文献

1
PLCB4 upregulation is associated with unfavorable prognosis in pediatric acute myeloid leukemia.磷脂酶Cβ4(PLCB4)上调与儿童急性髓系白血病的不良预后相关。
Oncol Lett. 2019 Dec;18(6):6057-6065. doi: 10.3892/ol.2019.10921. Epub 2019 Sep 25.
2
A six-gene leukemic stem cell score identifies high risk pediatric acute myeloid leukemia.六基因白血病干细胞评分可识别高风险儿科急性髓系白血病。
Leukemia. 2020 Mar;34(3):735-745. doi: 10.1038/s41375-019-0604-8. Epub 2019 Oct 23.
3
Mutations associated with a 17-gene leukemia stem cell score and the score's prognostic relevance in the context of the European LeukemiaNet classification of acute myeloid leukemia.
共受体神经纤毛蛋白-1通过血管内皮生长因子(VEGF)信号传导增强inv(16)急性髓系白血病中的增殖。
Leukemia. 2025 Feb;39(2):360-370. doi: 10.1038/s41375-024-02471-9. Epub 2024 Nov 21.
4
Chemotherapy resistance in acute myeloid leukemia is mediated by A20 suppression of spontaneous necroptosis.急性髓细胞白血病的化疗耐药性是由 A20 抑制自发坏死性凋亡介导的。
Nat Commun. 2024 Oct 24;15(1):9189. doi: 10.1038/s41467-024-53629-z.
5
Transcriptional Responses of Different Brain Cell Types to Oxygen Decline.不同脑细胞类型对氧含量下降的转录反应
Brain Sci. 2024 Mar 30;14(4):341. doi: 10.3390/brainsci14040341.
6
Prediction of immune infiltration and prognosis for patients with cholangiocarcinoma based on a cuproptosis-related lncRNA signature.基于铜死亡相关lncRNA特征预测胆管癌患者的免疫浸润和预后
Heliyon. 2023 Dec 20;10(1):e22774. doi: 10.1016/j.heliyon.2023.e22774. eCollection 2024 Jan 15.
7
Transcriptional Response to Standard AML Drugs Identifies Synergistic Combinations.转录反应对标准 AML 药物的鉴定表明存在协同组合。
Int J Mol Sci. 2023 Aug 18;24(16):12926. doi: 10.3390/ijms241612926.
8
Identifying a prognostic model and screening of potential natural compounds for acute myeloid leukemia.急性髓系白血病预后模型的识别及潜在天然化合物的筛选
Transl Cancer Res. 2023 Jun 30;12(6):1535-1551. doi: 10.21037/tcr-22-2500. Epub 2023 May 29.
9
Gene expression profiling unveils the temporal dynamics of CIGB-300-regulated transcriptome in AML cell lines.基因表达谱分析揭示了 CIGB-300 调节的 AML 细胞系转录组的时间动态。
BMC Genomics. 2023 Jul 4;24(1):373. doi: 10.1186/s12864-023-09472-5.
10
Role of Biomarkers in the Management of Acute Myeloid Leukemia.生物标志物在急性髓系白血病治疗中的作用。
Int J Mol Sci. 2022 Nov 22;23(23):14543. doi: 10.3390/ijms232314543.
与 17 基因白血病干细胞评分相关的突变及其在欧洲白血病网络急性髓细胞白血病分类中的预后相关性。
Haematologica. 2020 Mar;105(3):721-729. doi: 10.3324/haematol.2019.225003. Epub 2019 Aug 14.
4
Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype.基于图的基因组比对和基因分型与 HISAT2 和 HISAT-genotype。
Nat Biotechnol. 2019 Aug;37(8):907-915. doi: 10.1038/s41587-019-0201-4. Epub 2019 Aug 2.
5
Prognostic and Biologic Relevance of Clinically Applicable Long Noncoding RNA Profiling in Older Patients with Cytogenetically Normal Acute Myeloid Leukemia.临床适用的长链非编码 RNA 谱分析在细胞遗传学正常的老年急性髓系白血病患者中的预后和生物学相关性。
Mol Cancer Ther. 2019 Aug;18(8):1451-1459. doi: 10.1158/1535-7163.MCT-18-1125. Epub 2019 Jun 4.
6
ssExpression level of GAS6-mRNA influences the prognosis of acute myeloid leukemia patients with allogeneic hematopoietic stem cell transplantation.GAS6-mRNA 的表达水平影响异基因造血干细胞移植治疗急性髓系白血病患者的预后。
Biosci Rep. 2019 May 21;39(5). doi: 10.1042/BSR20190389. Print 2019 May 31.
7
Genome-wide association study identifies an acute myeloid leukemia susceptibility locus near BICRA.全基因组关联研究确定了BICRA附近的一个急性髓系白血病易感位点。
Leukemia. 2019 Mar;33(3):771-775. doi: 10.1038/s41375-018-0281-z. Epub 2018 Oct 5.
8
Gene Expression Detection Assay for Cancer Clinical Use.用于癌症临床应用的基因表达检测分析
J Cancer. 2018 Jun 5;9(13):2249-2265. doi: 10.7150/jca.24744. eCollection 2018.
9
Prognostic and biologic significance of long non-coding RNA profiling in younger adults with cytogenetically normal acute myeloid leukemia.年轻的细胞遗传学正常的急性髓系白血病患者长链非编码 RNA 谱分析的预后和生物学意义。
Haematologica. 2017 Aug;102(8):1391-1400. doi: 10.3324/haematol.2017.166215. Epub 2017 May 4.
10
The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.初发急性髓系白血病成年患者复发性细胞遗传学异常的突变肿瘤印记
Leukemia. 2017 Oct;31(10):2211-2218. doi: 10.1038/leu.2017.86. Epub 2017 Mar 24.