• 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

Successful treatment of acute promyelocytic leukemia with a t(X;17)(p11.4;q21) and BCOR-RARA fusion gene.

作者信息

Ichikawa Satoshi, Ichikawa Sonoko, Ishikawa Izumi, Takahashi Taro, Fujiwara Tohru, Harigae Hideo

机构信息

Department of Hematology, Osaki Citizen Hospital, Osaki, Japan; Department of Hematology and Rheumatology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Department of Hematology, Osaki Citizen Hospital, Osaki, Japan; Department of Medical Oncology, Osaki Citizen Hospital, Osaki, Japan.

出版信息

Cancer Genet. 2015 Apr;208(4):162-3. doi: 10.1016/j.cancergen.2015.01.008. Epub 2015 Feb 2.

DOI:10.1016/j.cancergen.2015.01.008
PMID:25790901
Abstract
摘要

相似文献

1
Successful treatment of acute promyelocytic leukemia with a t(X;17)(p11.4;q21) and BCOR-RARA fusion gene.采用t(X;17)(p11.4;q21)和BCOR-RARA融合基因成功治疗急性早幼粒细胞白血病。
Cancer Genet. 2015 Apr;208(4):162-3. doi: 10.1016/j.cancergen.2015.01.008. Epub 2015 Feb 2.
2
BCOR as a novel fusion partner of retinoic acid receptor alpha in a t(X;17)(p11;q12) variant of acute promyelocytic leukemia.BCOR 作为急性早幼粒细胞白血病 t(X;17)(p11;q12)变异型中 retinoic acid receptor alpha 的新型融合伙伴。
Blood. 2010 Nov 18;116(20):4274-83. doi: 10.1182/blood-2010-01-264432. Epub 2010 Aug 31.
3
Atypical response to all-trans retinoic acid in a der(5)t(5;17) acute promyelocytic leukemia.5号衍生染色体t(5;17)急性早幼粒细胞白血病对全反式维甲酸的非典型反应
Leukemia. 1999 Jun;13(6):862-8. doi: 10.1038/sj.leu.2401412.
4
GTF2I-RARA is a novel fusion transcript in a t(7;17) variant of acute promyelocytic leukaemia with clinical resistance to retinoic acid.GTF2I-RARA是急性早幼粒细胞白血病t(7;17)变异型中的一种新型融合转录本,对维甲酸具有临床耐药性。
Br J Haematol. 2015 Mar;168(6):904-8. doi: 10.1111/bjh.13157. Epub 2014 Oct 4.
5
[M3, promyelocytic leukemia].[M3,早幼粒细胞白血病]
Ryoikibetsu Shokogun Shirizu. 1998(22 Pt 3):65-7.
6
Isochromosome for derivative 17q in acute promyelocytic leukemia: evidence for two copies of PML-RARA and favorable response to all-trans-retinoic acid therapy.急性早幼粒细胞白血病中衍生17q等臂染色体:存在两个PML-RARA拷贝的证据及对全反式维甲酸治疗的良好反应。
Genes Chromosomes Cancer. 1997 Feb;18(2):151-3.
7
IRF2BP2-RARA t(1;17)(q42.3;q21.2) APL blasts differentiate in response to all-trans retinoic acid.IRF2BP2-RARA t(1;17)(q42.3;q21.2)急性早幼粒细胞白血病原始细胞对全反式维甲酸有反应并分化。
Leuk Lymphoma. 2018 Sep;59(9):2246-2249. doi: 10.1080/10428194.2017.1421761. Epub 2018 Jan 19.
8
Acute promyelocytic leukemia with PML-RARA fusion on i(17q) and therapy-related acute myeloid leukemia.伴有i(17q)上PML-RARA融合的急性早幼粒细胞白血病及治疗相关的急性髓系白血病。
Cancer Genet Cytogenet. 2005 Jun;159(2):129-36. doi: 10.1016/j.cancergencyto.2004.09.019.
9
A novel t(3;17)(p25;q21) variant translocation of acute promyelocytic leukemia with rearrangement of the RARA locus.一种伴有RARA基因座重排的急性早幼粒细胞白血病的新型t(3;17)(p25;q21)变异易位。
Leukemia. 2006 Feb;20(2):376-9. doi: 10.1038/sj.leu.2404062.
10
Retinoic acid regulatory pathways, chromosomal translocations, and acute promyelocytic leukemia.维甲酸调节通路、染色体易位与急性早幼粒细胞白血病
Genes Chromosomes Cancer. 1996 Mar;15(3):147-56. doi: 10.1002/(SICI)1098-2264(199603)15:3<147::AID-GCC1>3.0.CO;2-2.

引用本文的文献

1
Venetoclax combined with ATRA shows promising therapeutic potential for TFG:: RARA variant APL: a case report.维奈托克联合全反式维甲酸对TFG::RARA变异型急性早幼粒细胞白血病显示出有前景的治疗潜力:一例病例报告
Front Oncol. 2025 May 2;15:1529640. doi: 10.3389/fonc.2025.1529640. eCollection 2025.
2
Acute Promyelocytic Leukemia-like AML: Genetic Perspective and Clinical Implications.急性早幼粒细胞白血病样急性髓系白血病:遗传学视角与临床意义
Cancers (Basel). 2024 Dec 16;16(24):4192. doi: 10.3390/cancers16244192.
3
Case Report: Successful therapy with all- retinoic acid combined with chemotherapy followed by hematopoietic stem cell transplantation for acute promyelocytic leukemia carrying the fusion gene.
病例报告:全反式维甲酸联合化疗继以造血干细胞移植成功治疗携带融合基因的急性早幼粒细胞白血病。
Front Oncol. 2022 Sep 23;12:1013046. doi: 10.3389/fonc.2022.1013046. eCollection 2022.
4
Atypical Rearrangements in APL-Like Acute Myeloid Leukemias: Molecular Characterization and Prognosis.APL样急性髓系白血病中的非典型重排:分子特征与预后
Front Oncol. 2022 Apr 12;12:871590. doi: 10.3389/fonc.2022.871590. eCollection 2022.
5
Current views on the genetic landscape and management of variant acute promyelocytic leukemia.关于变异型急性早幼粒细胞白血病的遗传格局与管理的当前观点。
Biomark Res. 2021 May 6;9(1):33. doi: 10.1186/s40364-021-00284-x.
6
BCOR gene alterations in hematologic diseases.BCOR 基因改变与血液系统疾病。
Blood. 2021 Dec 16;138(24):2455-2468. doi: 10.1182/blood.2021010958.
7
PLZF-RAR, NPM1-RAR, and Other Acute Promyelocytic Leukemia Variants: The PETHEMA Registry Experience and Systematic Literature Review.PLZF-RAR、NPM1-RAR及其他急性早幼粒细胞白血病变异型:PETHEMA注册研究经验及系统文献综述
Cancers (Basel). 2020 May 21;12(5):1313. doi: 10.3390/cancers12051313.
8
Classic and Variants APLs, as Viewed from a Therapy Response.从治疗反应角度看经典型和变异型急性早幼粒细胞白血病
Cancers (Basel). 2020 Apr 14;12(4):967. doi: 10.3390/cancers12040967.
9
Acute Promyelocytic Leukemia: A Constellation of Molecular Events around a Single Fusion Gene.急性早幼粒细胞白血病:围绕单个融合基因的一系列分子事件
Cancers (Basel). 2020 Mar 8;12(3):624. doi: 10.3390/cancers12030624.
10
[Cytogenetic test and clinical study on cryptic acute promyelocytic leukemia with ins (15; 17)].隐匿性急性早幼粒细胞白血病伴插入(15;17)的细胞遗传学检测及临床研究
Zhonghua Xue Ye Xue Za Zhi. 2019 Oct 14;40(10):843-847. doi: 10.3760/cma.j.issn.0253-2727.2019.10.009.