• 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

基因内扩增:B 细胞前体急性淋巴细胞白血病中的一个新亚组?

Intragenic amplification of : a novel subgroup in B-cell precursor acute lymphoblastic leukemia?

作者信息

Schwab Claire, Nebral Karin, Chilton Lucy, Leschi Cristina, Waanders Esmé, Boer Judith M, Žaliová Markéta, Sutton Rosemary, Öfverholm Ingegerd Ivanov, Ohki Kentaro, Yamashita Yuka, Groeneveld-Krentz Stefanie, Froňková Eva, Bakkus Marleen, Tchinda Joelle, Barbosa Thayana da Conceição, Fazio Grazia, Mlynarski Wojciech, Pastorczak Agata, Cazzaniga Giovanni, Pombo-de-Oliveira Maria S, Trka Jan, Kirschner-Schwabe Renate, Imamura Toshihiko, Barbany Gisela, Stanulla Martin, Attarbaschi Andishe, Panzer-Grümayer Renate, Kuiper Roland P, den Boer Monique L, Cavé Hélène, Moorman Anthony V, Harrison Christine J, Strehl Sabine

机构信息

Leukaemia Research Cytogenetics Group, Wolfson Childhood Cancer Research Centre, Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne, United Kingdom.

Children's Cancer Research Institute, St Anna Kinderkrebsforschung, Vienna, Austria.

出版信息

Blood Adv. 2017 Aug 14;1(19):1473-1477. doi: 10.1182/bloodadvances.2017006734. eCollection 2017 Aug 22.

DOI:10.1182/bloodadvances.2017006734
PMID:29296789
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5728462/
Abstract

Intragenic amplification defines a novel, relapse-prone subtype of B-cell precursor acute lymphoblastic leukemia with a poor outcome.

摘要

基因内扩增定义了一种新的、易复发的B细胞前体急性淋巴细胞白血病亚型,其预后较差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a96/5728462/b21774bd3b2f/advances006734absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a96/5728462/b21774bd3b2f/advances006734absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a96/5728462/b21774bd3b2f/advances006734absf1.jpg

相似文献

1
Intragenic amplification of : a novel subgroup in B-cell precursor acute lymphoblastic leukemia?基因内扩增:B 细胞前体急性淋巴细胞白血病中的一个新亚组?
Blood Adv. 2017 Aug 14;1(19):1473-1477. doi: 10.1182/bloodadvances.2017006734. eCollection 2017 Aug 22.
2
Tumor suppressors BTG1 and IKZF1 cooperate during mouse leukemia development and increase relapse risk in B-cell precursor acute lymphoblastic leukemia patients.肿瘤抑制因子BTG1和IKZF1在小鼠白血病发展过程中协同作用,并增加B细胞前体急性淋巴细胞白血病患者的复发风险。
Haematologica. 2017 Mar;102(3):541-551. doi: 10.3324/haematol.2016.153023. Epub 2016 Dec 15.
3
The correlation between Pax5 deletion and patients survival in Iranian children with precursor B-cell acute lymphocytic leukemia.伊朗前体B细胞急性淋巴细胞白血病患儿中Pax5缺失与患者生存之间的相关性。
Cell Mol Biol (Noisy-le-grand). 2017 Aug 30;63(8):19-22. doi: 10.14715/cmb/2017.63.8.4.
4
Evaluation of multiplex ligation-dependent probe amplification as a method for the detection of copy number abnormalities in B-cell precursor acute lymphoblastic leukemia.多重连接依赖探针扩增法检测 B 细胞前体急性淋巴细胞白血病拷贝数异常的评价。
Genes Chromosomes Cancer. 2010 Dec;49(12):1104-13. doi: 10.1002/gcc.20818.
5
Minimal residual disease values discriminate between low and high relapse risk in children with B-cell precursor acute lymphoblastic leukemia and an intrachromosomal amplification of chromosome 21: the Austrian and German acute lymphoblastic leukemia Berlin-Frankfurt-Munster (ALL-BFM) trials.微小残留病值可区分21号染色体存在染色体内扩增的B细胞前体急性淋巴细胞白血病患儿的低复发风险和高复发风险:奥地利及德国急性淋巴细胞白血病柏林-法兰克福-明斯特(ALL-BFM)试验
J Clin Oncol. 2008 Jun 20;26(18):3046-50. doi: 10.1200/JCO.2008.16.1117.
6
The Genomic Landscape of PAX5, IKZF1, and CDKN2A/B Alterations in B-Cell Precursor Acute Lymphoblastic Leukemia.B细胞前体急性淋巴细胞白血病中PAX5、IKZF1和CDKN2A/B基因改变的基因组格局
Cytogenet Genome Res. 2016;150(3-4):242-252. doi: 10.1159/000456572. Epub 2017 Feb 18.
7
Evaluation of PAX5 gene in the early stages of leukemic B cells in the childhood B cell acute lymphoblastic leukemia.评价 PAX5 基因在儿童 B 细胞急性淋巴细胞白血病白血病性 B 细胞早期阶段的作用。
Leuk Res. 2012 Jan;36(1):87-92. doi: 10.1016/j.leukres.2011.07.017. Epub 2011 Aug 2.
8
Incidence and diversity of PAX5 fusion genes in childhood acute lymphoblastic leukemia.儿童急性淋巴细胞白血病中PAX5融合基因的发生率及多样性
Leukemia. 2009 Jan;23(1):134-43. doi: 10.1038/leu.2008.306. Epub 2008 Nov 20.
9
Ph-like acute lymphoblastic leukemia with a novel PAX5-KIDINS220 fusion transcript.具有新型PAX5-KIDINS220融合转录本的Ph样急性淋巴细胞白血病
Genes Chromosomes Cancer. 2017 Apr;56(4):278-284. doi: 10.1002/gcc.22433. Epub 2016 Nov 21.
10
Copy number profiling of adult relapsed B-cell precursor acute lymphoblastic leukemia reveals potential leukemia progression mechanisms.成人复发性B细胞前体急性淋巴细胞白血病的拷贝数分析揭示了潜在的白血病进展机制。
Genes Chromosomes Cancer. 2017 Nov;56(11):810-820. doi: 10.1002/gcc.22486. Epub 2017 Aug 26.

引用本文的文献

1
Application of Omics Analyses in Pediatric B-Cell Acute Lymphoblastic Leukemia.组学分析在儿童B细胞急性淋巴细胞白血病中的应用
Biomedicines. 2025 Feb 10;13(2):424. doi: 10.3390/biomedicines13020424.
2
PAX5::AUTS2 childhood B-ALL: a relapse-prone genetic subtype with frequent central nervous system involvement and a poor outcome.PAX5::AUTS2儿童B细胞急性淋巴细胞白血病:一种易复发的遗传亚型,常累及中枢神经系统且预后不良。
Leukemia. 2025 Feb;39(2):482-486. doi: 10.1038/s41375-024-02502-5. Epub 2024 Dec 19.
3
Unraveling the Genetic Heterogeneity of Acute Lymphoblastic Leukemia Based on NGS Applications.

本文引用的文献

1
gene rearrangement as a subclonal change in -positive B-cell acute lymphoblastic leukemia.基因重排作为阳性B淋巴细胞急性淋巴细胞白血病中的亚克隆变化。
Blood Adv. 2016 Nov 30;1(2):132-138. doi: 10.1182/bloodadvances.2016000463. eCollection 2016 Dec 13.
2
A novel integrated cytogenetic and genomic classification refines risk stratification in pediatric acute lymphoblastic leukemia.一种新型的综合细胞遗传学和基因组分类方法可细化儿童急性淋巴细胞白血病的风险分层。
Blood. 2014 Aug 28;124(9):1434-44. doi: 10.1182/blood-2014-03-562918. Epub 2014 Jun 23.
3
Functional heterogeneity of PAX5 chimeras reveals insight for leukemia development.
基于二代测序技术应用解析急性淋巴细胞白血病的遗传异质性
Cancers (Basel). 2024 Nov 26;16(23):3965. doi: 10.3390/cancers16233965.
4
Copy number alterations in pediatric B-cell precursor acute lymphoblastic leukemia patients and their association with patients' outcome.儿童B细胞前体急性淋巴细胞白血病患者的拷贝数改变及其与患者预后的关联。
Ann Hematol. 2025 Mar;104(3):1821-1832. doi: 10.1007/s00277-024-06102-2. Epub 2024 Nov 26.
5
is a frequent biomarker of adverse prognosis in Mexican pediatric patients with B-acute lymphoblastic leukemia.在患有B型急性淋巴细胞白血病的墨西哥儿科患者中,是不良预后的常见生物标志物。
Front Oncol. 2024 Apr 3;14:1337954. doi: 10.3389/fonc.2024.1337954. eCollection 2024.
6
Alterations in a Consecutive Childhood B-Cell Acute Lymphoblastic Leukemia Cohort Treated Using the ALL IC-BFM 2009 Protocol.采用ALL IC-BFM 2009方案治疗的连续性儿童B细胞急性淋巴细胞白血病队列中的改变
Cancers (Basel). 2024 Mar 15;16(6):1164. doi: 10.3390/cancers16061164.
7
Expanding the Clinical Utility of Targeted RNA Sequencing Panels beyond Gene Fusions to Complex, Intragenic Structural Rearrangements.将靶向RNA测序面板的临床应用从基因融合扩展到复杂的基因内结构重排。
Cancers (Basel). 2023 Sep 2;15(17):4394. doi: 10.3390/cancers15174394.
8
Transcription factor networks link B-lymphocyte development and malignant transformation in leukemia.转录因子网络将白血病中的 B 淋巴细胞发育和恶性转化联系起来。
Genes Dev. 2023 Aug 1;37(15-16):703-723. doi: 10.1101/gad.349879.122. Epub 2023 Sep 6.
9
alterations in B-cell acute lymphoblastic leukemia.B细胞急性淋巴细胞白血病的改变
Front Oncol. 2022 Oct 25;12:1023606. doi: 10.3389/fonc.2022.1023606. eCollection 2022.
10
Allelic complexity of KMT2A partial tandem duplications in acute myeloid leukemia and myelodysplastic syndromes.急性髓系白血病和骨髓增生异常综合征中KMT2A部分串联重复的等位基因复杂性
Blood Adv. 2022 Jul 26;6(14):4236-4240. doi: 10.1182/bloodadvances.2022007613.
PAX5嵌合体的功能异质性为白血病发展提供了见解。
Mol Cancer Res. 2014 Apr;12(4):595-606. doi: 10.1158/1541-7786.MCR-13-0337. Epub 2014 Jan 16.
4
Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A.由PAX5基因c.547G>A的种系传递导致的前体B细胞急性淋巴细胞白血病的遗传易感性。
Leukemia. 2014 May;28(5):1136-8. doi: 10.1038/leu.2013.363. Epub 2013 Nov 29.
5
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia.一种反复出现的 PAX5 种系突变可导致前 B 细胞急性淋巴细胞白血病易感性。
Nat Genet. 2013 Oct;45(10):1226-1231. doi: 10.1038/ng.2754. Epub 2013 Sep 8.
6
Independent prognostic value of BCR-ABL1-like signature and IKZF1 deletion, but not high CRLF2 expression, in children with B-cell precursor ALL.BCR-ABL1 样特征和 IKZF1 缺失而非高 CRLF2 表达对儿童 B 细胞前体 ALL 具有独立预后价值。
Blood. 2013 Oct 10;122(15):2622-9. doi: 10.1182/blood-2012-10-462358. Epub 2013 Aug 23.
7
Relapsed childhood acute lymphoblastic leukaemia.复发型儿童急性淋巴细胞白血病。
Lancet Oncol. 2013 May;14(6):e205-17. doi: 10.1016/S1470-2045(12)70580-6.
8
Impact of IKZF1 deletions and PAX5 amplifications in pediatric B-cell precursor ALL treated according to NOPHO protocols.根据北欧儿科血液学和肿瘤学会(NOPHO)方案治疗的儿童B细胞前体急性淋巴细胞白血病中IKZF1缺失和PAX5扩增的影响
Leukemia. 2013 Sep;27(9):1936-9. doi: 10.1038/leu.2013.92. Epub 2013 Mar 29.
9
Genes commonly deleted in childhood B-cell precursor acute lymphoblastic leukemia: association with cytogenetics and clinical features.儿童 B 细胞前体急性淋巴细胞白血病中常见缺失的基因:与细胞遗传学和临床特征的关联。
Haematologica. 2013 Jul;98(7):1081-8. doi: 10.3324/haematol.2013.085175. Epub 2013 Mar 18.
10
Small sizes and indolent evolutionary dynamics challenge the potential role of P2RY8-CRLF2-harboring clones as main relapse-driving force in childhood ALL.小尺寸和惰性进化动力学挑战了 P2RY8-CRLF2 携带克隆作为儿童 ALL 主要复发驱动因素的潜在作用。
Blood. 2012 Dec 20;120(26):5134-42. doi: 10.1182/blood-2012-07-443218. Epub 2012 Oct 22.