• 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

源自人类急性髓系白血病细胞系的诱导多能干细胞系(HL-60-iPSC)保留白血病异常特征并表现出髓系分化缺陷。

An iPSC line derived from a human acute myeloid leukemia cell line (HL-60-iPSC) retains leukemic abnormalities and displays myeloid differentiation defects.

作者信息

Yamasaki Amanda E, Warshaw Jane N, Kyalwazi Beverly L, Matsui Hiroko, Jepsen Kristen, Panopoulos Athanasia D

机构信息

Department of Biological Sciences, University of Notre Dame, IN 46556, USA; Center for Stem Cells and Regenerative Medicine, University of Notre Dame, IN 46556, USA.

Department of Biological Sciences, University of Notre Dame, IN 46556, USA.

出版信息

Stem Cell Res. 2020 Dec;49:102096. doi: 10.1016/j.scr.2020.102096. Epub 2020 Nov 23.

DOI:10.1016/j.scr.2020.102096
PMID:33370871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8031422/
Abstract

Cancer-derived iPSCs have provided valuable insight into oncogenesis, but human cancer cells can often be difficult to reprogram, especially in cases of complex genetic abnormalities. Here we report, to our knowledge, the first successful generation of an iPSC line from a human immortalized acute myeloid leukemia (AML) cell line, the cell line HL-60. This iPSC line retains a majority of the leukemic genotype and displays defects in myeloid differentiation, thus providing a tool for modeling and studying AML.

摘要

癌症衍生的诱导多能干细胞为肿瘤发生提供了有价值的见解,但人类癌细胞往往难以重编程,尤其是在复杂基因异常的情况下。据我们所知,在此我们报告首次成功从人类永生化急性髓系白血病(AML)细胞系HL-60生成了诱导多能干细胞系。该诱导多能干细胞系保留了大部分白血病基因型,并在髓系分化方面存在缺陷,从而为AML的建模和研究提供了一个工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8499/8031422/8b96a388ec86/nihms-1658120-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8499/8031422/8b96a388ec86/nihms-1658120-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8499/8031422/8b96a388ec86/nihms-1658120-f0001.jpg

相似文献

1
An iPSC line derived from a human acute myeloid leukemia cell line (HL-60-iPSC) retains leukemic abnormalities and displays myeloid differentiation defects.源自人类急性髓系白血病细胞系的诱导多能干细胞系(HL-60-iPSC)保留白血病异常特征并表现出髓系分化缺陷。
Stem Cell Res. 2020 Dec;49:102096. doi: 10.1016/j.scr.2020.102096. Epub 2020 Nov 23.
2
Modeling Leukemia Stem Cells with Patient-Derived Induced Pluripotent Stem Cells.利用患者来源的诱导多能干细胞建立白血病干细胞模型。
Methods Mol Biol. 2021;2185:411-422. doi: 10.1007/978-1-0716-0810-4_26.
3
Human AML-iPSCs Reacquire Leukemic Properties after Differentiation and Model Clonal Variation of Disease.人类急性髓系白血病诱导多能干细胞在分化后重新获得白血病特性并模拟疾病的克隆变异。
Cell Stem Cell. 2017 Mar 2;20(3):329-344.e7. doi: 10.1016/j.stem.2016.11.018. Epub 2017 Jan 12.
4
Reprogramming of Acute Myeloid Leukemia Patients Cells: Harboring Cancer Mutations Requires Targeting of AML Hierarchy.急性髓系白血病患者细胞的重编程:携带癌症突变需要靶向 AML 层级。
Stem Cells Transl Med. 2023 Jun 15;12(6):334-354. doi: 10.1093/stcltm/szad022.
5
Two iPSC lines generated from the bone marrow of a relapsed/refractory AML patient display normal karyotypes and myeloid differentiation potential.从一名复发/难治性急性髓系白血病(AML)患者的骨髓中产生的两条诱导多能干细胞(iPSC)系显示出正常的核型和髓系分化潜能。
Stem Cell Res. 2019 Dec;41:101587. doi: 10.1016/j.scr.2019.101587. Epub 2019 Oct 17.
6
An induced pluripotent stem cell t(7;12)(q36;p13) acute myeloid leukemia model shows high expression of MNX1 and a block in differentiation of the erythroid and megakaryocytic lineages.诱导多能干细胞 t(7;12)(q36;p13) 急性髓系白血病模型显示 MNX1 高表达,并阻断红系和巨核细胞谱系的分化。
Int J Cancer. 2022 Sep 1;151(5):770-782. doi: 10.1002/ijc.34122. Epub 2022 Jun 3.
7
Modeling leukemia with pediatric acute leukemia patient-derived iPSCs.利用儿科急性白血病患者来源的诱导多能干细胞建立白血病模型。
Stem Cell Res. 2021 Jul;54:102404. doi: 10.1016/j.scr.2021.102404. Epub 2021 May 25.
8
Patient-Derived iPSCs Faithfully Represent the Genetic Diversity and Cellular Architecture of Human Acute Myeloid Leukemia.患者来源的 iPSCs 忠实地代表了人类急性髓细胞白血病的遗传多样性和细胞结构。
Blood Cancer Discov. 2023 Jul 5;4(4):318-335. doi: 10.1158/2643-3230.BCD-22-0167.
9
Brief Report: Human Acute Myeloid Leukemia Reprogramming to Pluripotency Is a Rare Event and Selects for Patient Hematopoietic Cells Devoid of Leukemic Mutations.简要报告:人类急性髓系白血病重编程为多能性是一个罕见事件,并选择了缺乏白血病突变的患者造血细胞。
Stem Cells. 2017 Sep;35(9):2095-2102. doi: 10.1002/stem.2655. Epub 2017 Jul 31.
10
iPSC Models of Leukemia Come of Age.iPSC 模型在白血病研究中的应用日趋成熟。
Blood Cancer Discov. 2023 Jul 5;4(4):252-253. doi: 10.1158/2643-3230.BCD-23-0041.

引用本文的文献

1
The Immune Resistance Signature of Acute Myeloid Leukemia and Current Immunotherapy Strategies.急性髓系白血病的免疫抵抗特征及当前免疫治疗策略
Cancers (Basel). 2024 Jul 23;16(15):2615. doi: 10.3390/cancers16152615.
2
Development of 3D-iNET ORION: a novel, pre-clinical, three-dimensional in vitro cell model for modeling human metastatic neuroendocrine tumor of the pancreas.3D-iNET ORION 的研发:一种新型的、临床前的、用于模拟人胰腺转移性神经内分泌肿瘤的三维体外细胞模型。
Hum Cell. 2024 Sep;37(5):1593-1601. doi: 10.1007/s13577-024-01113-7. Epub 2024 Aug 5.
3
Reprogramming of Acute Myeloid Leukemia Patients Cells: Harboring Cancer Mutations Requires Targeting of AML Hierarchy.

本文引用的文献

1
High-Throughput and Cost-Effective Characterization of Induced Pluripotent Stem Cells.高通量且经济高效的诱导多能干细胞表征。
Stem Cell Reports. 2017 Apr 11;8(4):1101-1111. doi: 10.1016/j.stemcr.2017.03.011.
2
iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types.iPSCORE:一个包含 222 个人诱导多能干细胞系的资源库,能够对多种细胞类型中的遗传变异进行功能特征分析。
Stem Cell Reports. 2017 Apr 11;8(4):1086-1100. doi: 10.1016/j.stemcr.2017.03.012.
3
Hematopoietic differentiation and production of mature myeloid cells from human pluripotent stem cells.
急性髓系白血病患者细胞的重编程:携带癌症突变需要靶向 AML 层级。
Stem Cells Transl Med. 2023 Jun 15;12(6):334-354. doi: 10.1093/stcltm/szad022.
4
Shikonin as a WT1 Inhibitor Promotes Promyeloid Leukemia Cell Differentiation.紫草素作为 WT1 抑制剂促进早幼粒细胞白血病细胞分化。
Molecules. 2022 Nov 26;27(23):8264. doi: 10.3390/molecules27238264.
5
Are Induced Pluripotent Stem Cells a Step towards Modeling Pediatric Leukemias?诱导多能干细胞是否是模拟儿科白血病的一个步骤?
Cells. 2022 Jan 29;11(3):476. doi: 10.3390/cells11030476.
人多能干细胞向造血细胞分化及向成熟髓系细胞生成。
Nat Protoc. 2011 Mar;6(3):296-313. doi: 10.1038/nprot.2010.184. Epub 2011 Feb 17.
4
HL-60 cell line was derived from a patient with FAB-M2 and not FAB-M3.HL-60细胞系源自一名患有FAB-M2而非FAB-M3的患者。
Blood. 1988 Jan;71(1):242-7.
5
Characterization of the continuous, differentiating myeloid cell line (HL-60) from a patient with acute promyelocytic leukemia.对一名急性早幼粒细胞白血病患者的连续分化髓系细胞系(HL-60)的特征描述。
Blood. 1979 Sep;54(3):713-33.