• 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

Cytogenetic characterization of putative human myeloblastic leukemia cell lines (ML-1, -2, and -3): origin of the cells.

作者信息

Ohyashiki K, Ohyashiki J H, Sandberg A A

出版信息

Cancer Res. 1986 Jul;46(7):3642-7.

PMID:3458526
Abstract

Cytogenetic studies were performed on ML cell lines (ML-1, -2, and -3), as well as on the leukemic cells of a patient from whom the ML cells were derived. The ML-1 cell line showed numerical and structural cytogenetic changes, i.e., -Y, 1p-, 6q-, 11q-, +12, +13q+, 14q-, and 17q-. The ML-2 cell line had two copies of the 13q+, whereas the ML-3 cells contained three clones, i.e., 47,X,-Y,1p-,6q-,11q-,+12,+13q+, 48,X,-Y,1p-,6q-,+6q-,11q-,+12,+13q+, and 49,X,-Y,1p-,6q-,+6q-, 11q-,+12,+13q+,+13q+. The neoplastic cells, when the patient was diagnosed as having T-cell malignant lymphoma (Stage IV), had the 11q- and 13q+. The leukemic cells in a subsequent acute myeloid leukemia phase of this patient contained structural (1p- and 6q-) and numerical (+12, -Y and +2D-group chromosomes: two 13q+) changes in addition to the 11q-. These findings suggest that the acute myeloid leukemic cells of this patient probably originated from the neoplastic cells of the preceding T-cell lymphoma, and that the chromosome changes originally seen in the lymphoma cells were preserved in the established ML cell lines, though the cells of these lines had myeloid characteristics.

摘要

相似文献

1
Cytogenetic characterization of putative human myeloblastic leukemia cell lines (ML-1, -2, and -3): origin of the cells.
Cancer Res. 1986 Jul;46(7):3642-7.
2
Chromosome abnormalities in leukemia and lymphoma.白血病和淋巴瘤中的染色体异常。
Ann Clin Lab Sci. 1983 Mar-Apr;13(2):87-94.
3
Chromosome abnormalities in adult T-cell leukemia/lymphoma: a karyotype review committee report.
Cancer Res. 1992 Mar 15;52(6):1481-93.
4
Characterization of a novel malignant B cell line with t(14;18) and t(4;11) established from a patient with acute monoblastic leukemia.从一名急性单核细胞白血病患者建立的具有t(14;18)和t(4;11)的新型恶性B细胞系的特征分析
Exp Hematol. 1997 Sep;25(10):1062-8.
5
A case of acute myeloblastic leukemia with chromosomes showing 46, XY = 11/46, XY, 21q- = 39.一例急性髓细胞白血病患者,其染色体显示为46,XY = 11/46,XY,21q- = 39。
Tokai J Exp Clin Med. 1980 Jan;5(1):45-50.
6
Comprehensive molecular cytogenetic characterization of cervical cancer cell lines.宫颈癌细胞系的全面分子细胞遗传学特征分析
Genes Chromosomes Cancer. 2003 Mar;36(3):233-41. doi: 10.1002/gcc.10158.
7
Jumping translocations in hematological malignancies: a cytogenetic study of five cases.血液系统恶性肿瘤中的跳跃式易位:5例细胞遗传学研究
Cancer Genet Cytogenet. 2008 Dec;187(2):85-94. doi: 10.1016/j.cancergencyto.2008.07.010.
8
Correlation between cytogenetic abnormalities and disease characteristics in multiple myeloma: monosomy of chromosome 13 and structural abnormalities of 11q are associated with a high percentage of S-phase plasma cells.多发性骨髓瘤细胞遗传学异常与疾病特征之间的相关性:13号染色体单体和11q结构异常与高比例的S期浆细胞相关。
Haematologica. 2000 Nov;85(11):1146-52.
9
Combined spectral karyotyping, comparative genomic hybridization, and in vitro apoptyping of a panel of Burkitt's lymphoma-derived B cell lines reveals an unexpected complexity of chromosomal aberrations and a recurrence of specific abnormalities in chemoresistant cell lines.对一组伯基特淋巴瘤来源的B细胞系进行联合光谱核型分析、比较基因组杂交和体外凋亡分析,揭示了染色体畸变的意外复杂性以及化疗耐药细胞系中特定异常的复发情况。
Int J Oncol. 2006 Mar;28(3):605-17.
10
Molecular cytogenetic characterization of the KG-1 and KG-1a acute myeloid leukemia cell lines by use of spectral karyotyping and fluorescence in situ hybridization.利用光谱核型分析和荧光原位杂交技术对KG-1和KG-1a急性髓性白血病细胞系进行分子细胞遗传学特征分析。
Genes Chromosomes Cancer. 2003 Nov;38(3):249-52. doi: 10.1002/gcc.10274.

引用本文的文献

1
The MLL/SET family and haematopoiesis.MLL/SET 家族与造血。
Biochim Biophys Acta Gene Regul Mech. 2020 Aug;1863(8):194579. doi: 10.1016/j.bbagrm.2020.194579. Epub 2020 May 7.
2
H3K79me2/3 controls enhancer-promoter interactions and activation of the pan-cancer stem cell marker PROM1/CD133 in MLL-AF4 leukemia cells.H3K79me2/3 控制增强子-启动子相互作用,并激活 MLL-AF4 白血病细胞中的泛癌干细胞标记物 PROM1/CD133。
Leukemia. 2021 Jan;35(1):90-106. doi: 10.1038/s41375-020-0808-y. Epub 2020 Apr 2.
3
A Menin-MLL Inhibitor Induces Specific Chromatin Changes and Eradicates Disease in Models of MLL-Rearranged Leukemia.
一种 Menin-MLL 抑制剂可诱导特定的染色质变化,并消除 MLL 重排白血病模型中的疾病。
Cancer Cell. 2019 Dec 9;36(6):660-673.e11. doi: 10.1016/j.ccell.2019.11.001.
4
DOT1L inhibition reveals a distinct subset of enhancers dependent on H3K79 methylation.DOT1L 抑制揭示了依赖于 H3K79 甲基化的独特增强子亚群。
Nat Commun. 2019 Jun 26;10(1):2803. doi: 10.1038/s41467-019-10844-3.
5
MLL2, Not MLL1, Plays a Major Role in Sustaining MLL-Rearranged Acute Myeloid Leukemia.MLL2而非MLL1在维持MLL重排的急性髓系白血病中起主要作用。
Cancer Cell. 2017 Jun 12;31(6):755-770.e6. doi: 10.1016/j.ccell.2017.05.002.
6
Reovirus-mediated cytotoxicity and enhancement of innate immune responses against acute myeloid leukemia.呼肠孤病毒介导的细胞毒性作用及对急性髓系白血病先天性免疫反应的增强作用。
Biores Open Access. 2012 Jan;1(1):3-15. doi: 10.1089/biores.2012.0205.
7
RUNX1 is a key target in t(4;11) leukemias that contributes to gene activation through an AF4-MLL complex interaction.RUNX1 是 t(4;11) 白血病的关键靶点,通过 AF4-MLL 复合物相互作用促进基因激活。
Cell Rep. 2013 Jan 31;3(1):116-27. doi: 10.1016/j.celrep.2012.12.016. Epub 2013 Jan 24.
8
Targeting AML through DR4 with a novel variant of rhTRAIL.通过新型 rhTRAIL 靶向 DR4 治疗 AML。
J Cell Mol Med. 2011 Oct;15(10):2216-31. doi: 10.1111/j.1582-4934.2010.01211.x.
9
Protein Tyrosine Phosphatase Gamma (PTPgamma) is a Novel Leukocyte Marker Highly Expressed by CD34 Precursors.蛋白酪氨酸磷酸酶γ(PTPγ)是一种由CD34前体细胞高度表达的新型白细胞标志物。
Biomark Insights. 2007 May 31;2:218-25.
10
Use of HL-60 cell line to measure opsonic capacity of pneumococcal antibodies.使用HL-60细胞系测量肺炎球菌抗体的调理吞噬能力。
Clin Diagn Lab Immunol. 2005 Jan;12(1):19-27. doi: 10.1128/CDLI.12.1.19-27.2005.