• 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

遗传学和表观遗传学在急性髓系白血病中的诊断及临床影响

The diagnostic and clinical impact of genetics and epigenetics in acute myeloid leukemia.

作者信息

Ohgami R S, Arber D A

机构信息

Stanford University, Stanford, CA, USA.

出版信息

Int J Lab Hematol. 2015 May;37 Suppl 1:122-32. doi: 10.1111/ijlh.12367.

DOI:10.1111/ijlh.12367
PMID:25976970
Abstract

Acute myeloid leukemia (AML) is a complex disease, for which our understanding of the role of genetic and epigenetic changes has undergone significant advancements. Newer diagnostic and prognostic classifications have increasingly incorporated such information, and novel therapies have been developed to target specific genes, processes, and pathways based on this growing understanding. Given the rapid evolution of this field, it is critical for physicians and translational researchers to have a more in-depth understanding of this evolving landscape. Here, we review both genetics and epigenetics in acute myeloid leukemia from a practical standpoint.

摘要

急性髓系白血病(AML)是一种复杂的疾病,我们对其遗传和表观遗传变化所起作用的理解已经取得了重大进展。更新的诊断和预后分类越来越多地纳入了此类信息,并且基于这种不断加深的理解,已经开发出了针对特定基因、过程和通路的新型疗法。鉴于该领域的快速发展,医生和转化研究人员更深入地了解这一不断演变的情况至关重要。在此,我们从实际应用的角度综述急性髓系白血病中的遗传学和表观遗传学。

相似文献

1
The diagnostic and clinical impact of genetics and epigenetics in acute myeloid leukemia.遗传学和表观遗传学在急性髓系白血病中的诊断及临床影响
Int J Lab Hematol. 2015 May;37 Suppl 1:122-32. doi: 10.1111/ijlh.12367.
2
The increasing genomic complexity of acute myeloid leukemia.急性髓系白血病日益增加的基因组复杂性。
Best Pract Res Clin Haematol. 2014 Sep-Dec;27(3-4):209-13. doi: 10.1016/j.beha.2014.10.001. Epub 2014 Oct 15.
3
Acute myeloid leukemia: advances in diagnosis and classification.急性髓细胞白血病:诊断和分类的进展。
Int J Lab Hematol. 2013 Jun;35(3):358-66. doi: 10.1111/ijlh.12081.
4
Acute myeloid leukemia with mutated NPM1: diagnosis, prognosis and therapeutic perspectives.伴 NPM1 基因突变的急性髓系白血病:诊断、预后和治疗前景。
Curr Opin Oncol. 2009 Nov;21(6):573-81. doi: 10.1097/CCO.0b013e3283313dfa.
5
Acute myeloid leukemia with t(8;21)/AML1/ETO: a distinct biological and clinical entity.伴有t(8;21)/AML1/ETO的急性髓系白血病:一种独特的生物学和临床实体。
Haematologica. 2002 Mar;87(3):306-19.
6
Identification of truncated RUNX1 and RUNX1-PRDM16 fusion transcripts in a case of t(1;21)(p36;q22)-positive therapy-related AML.在一例t(1;21)(p36;q22)阳性的治疗相关急性髓系白血病病例中截短型RUNX1和RUNX1-PRDM16融合转录本的鉴定
Leukemia. 2006 Jun;20(6):1187-9. doi: 10.1038/sj.leu.2404210.
7
Detection of MOZ-CBP fusion in acute myeloid leukemia with 8;16 translocation.
Leukemia. 2005 Dec;19(12):2344-5. doi: 10.1038/sj.leu.2403971.
8
Fusion gene transcripts and Ig/TCR gene rearrangements are complementary but infrequent targets for PCR-based detection of minimal residual disease in acute myeloid leukemia.融合基因转录本和Ig/TCR基因重排是基于PCR检测急性髓系白血病微小残留病的互补但不常见的靶点。
Leukemia. 2002 Mar;16(3):368-75. doi: 10.1038/sj.leu.2402387.
9
Prognostic impact of t(9;11) in childhood acute myeloid leukemia (AML).
Leukemia. 2003 Mar;17(3):636. doi: 10.1038/sj.leu.2402846.
10
Acute Myeloid Leukemia Genetics: Risk Stratification and Implications for Therapy.急性髓系白血病遗传学:风险分层及其对治疗的意义。
Arch Pathol Lab Med. 2015 Oct;139(10):1215-23. doi: 10.5858/arpa.2015-0203-RA.

引用本文的文献

1
Traditional Chinese medicine for acute myelocytic leukemia therapy: exploiting epigenetic targets.用于急性髓细胞白血病治疗的中药:靶向表观遗传靶点
Front Pharmacol. 2024 Jun 4;15:1388903. doi: 10.3389/fphar.2024.1388903. eCollection 2024.
2
Lower Levels of TET2 Gene Expression, with a Higher Level of TET2 Promoter Methylation in Patients with AML; Evidence for the Role of Aberrant Methylation in AML Pathogenesis.急性髓系白血病患者中TET2基因表达水平较低,TET2启动子甲基化水平较高;异常甲基化在急性髓系白血病发病机制中的作用证据。
Indian J Hematol Blood Transfus. 2024 Jan;40(1):52-60. doi: 10.1007/s12288-023-01673-y. Epub 2023 Jun 5.
3
Reduced expression of lncRNA DLEU7-AS1 is a novel favorable prognostic factor in acute myeloid leukemia.
lncRNA DLEU7-AS1 低表达是急性髓系白血病的一个新的有利预后因素。
Biosci Rep. 2022 May 27;42(5). doi: 10.1042/BSR20212078.
4
ENL: structure, function, and roles in hematopoiesis and acute myeloid leukemia.ENL:在造血和急性髓系白血病中的结构、功能和作用。
Cell Mol Life Sci. 2018 Nov;75(21):3931-3941. doi: 10.1007/s00018-018-2895-8. Epub 2018 Jul 31.
5
Clinical implications of genome-wide DNA methylation studies in acute myeloid leukemia.全基因组DNA甲基化研究在急性髓系白血病中的临床意义
J Hematol Oncol. 2017 Feb 2;10(1):41. doi: 10.1186/s13045-017-0409-z.
6
Transcriptional Auto-Regulation of RUNX1 P1 Promoter.RUNX1 P1启动子的转录自调控
PLoS One. 2016 Feb 22;11(2):e0149119. doi: 10.1371/journal.pone.0149119. eCollection 2016.
7
Clinical evaluation of panel testing by next-generation sequencing (NGS) for gene mutations in myeloid neoplasms.采用新一代测序(NGS)进行髓系肿瘤基因突变的panel检测的临床评估。
Diagn Pathol. 2016 Jan 22;11:11. doi: 10.1186/s13000-016-0456-8.