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1
Gene expression profiling and candidate gene resequencing identifies pathways and mutations important for malignant transformation caused by leukemogenic fusion genes.基因表达谱分析和候选基因重测序确定了导致白血病融合基因恶性转化的重要途径和突变。
Exp Hematol. 2012 Dec;40(12):1016-27. doi: 10.1016/j.exphem.2012.08.001. Epub 2012 Aug 8.
2
NUP98 gene fusions and hematopoietic malignancies: common themes and new biologic insights.NUP98 基因融合与血液系统恶性肿瘤:共同主题与新的生物学见解。
Blood. 2011 Dec 8;118(24):6247-57. doi: 10.1182/blood-2011-07-328880. Epub 2011 Sep 26.
3
Cell of origin in AML: susceptibility to MN1-induced transformation is regulated by the MEIS1/AbdB-like HOX protein complex.急性髓系白血病的起源细胞:MN1 诱导的转化易感性受 MEIS1/AbdB 样 HOX 蛋白复合物的调节。
Cancer Cell. 2011 Jul 12;20(1):39-52. doi: 10.1016/j.ccr.2011.06.020.
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Expression of miR-196b is not exclusively MLL-driven but is especially linked to activation of HOXA genes in pediatric acute lymphoblastic leukemia.miR-196b 的表达并非完全由 MLL 驱动,而是与小儿急性淋巴细胞白血病中 HOXA 基因的激活特别相关。
Haematologica. 2010 Oct;95(10):1675-82. doi: 10.3324/haematol.2010.023481. Epub 2010 May 21.
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The OP9-DL1 system: generation of T-lymphocytes from embryonic or hematopoietic stem cells in vitro.OP9-DL1系统:体外从胚胎干细胞或造血干细胞生成T淋巴细胞。
Cold Spring Harb Protoc. 2009 Feb;2009(2):pdb.prot5156. doi: 10.1101/pdb.prot5156.
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A NUP98-HOXD13 fusion gene impairs differentiation of B and T lymphocytes and leads to expansion of thymocytes with partial TCRB gene rearrangement.NUP98-HOXD13融合基因损害B淋巴细胞和T淋巴细胞的分化,并导致部分TCRB基因重排的胸腺细胞扩增。
J Immunol. 2009 Nov 15;183(10):6227-35. doi: 10.4049/jimmunol.0901121. Epub 2009 Oct 19.
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Haematopoietic malignancies caused by dysregulation of a chromatin-binding PHD finger.由染色质结合的PHD指结构域失调引起的造血系统恶性肿瘤。
Nature. 2009 Jun 11;459(7248):847-51. doi: 10.1038/nature08036.
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Regulation of mir-196b by MLL and its overexpression by MLL fusions contributes to immortalization.MLL对mir-196b的调控及其通过MLL融合导致的过表达有助于细胞永生化。
Blood. 2009 Apr 2;113(14):3314-22. doi: 10.1182/blood-2008-04-154310. Epub 2009 Feb 2.
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Chromosomal rearrangements leading to MLL gene fusions: clinical and biological aspects.导致MLL基因融合的染色体重排:临床与生物学方面
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10
HOXA9 is required for survival in human MLL-rearranged acute leukemias.HOXA9对于人类MLL重排急性白血病的存活是必需的。
Blood. 2009 Mar 12;113(11):2375-85. doi: 10.1182/blood-2007-09-113597. Epub 2008 Dec 3.

单独过表达 Hoxa9 易导致淋巴性而非髓性白血病的发生。

Isolated Hoxa9 overexpression predisposes to the development of lymphoid but not myeloid leukemia.

机构信息

Genetics Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Exp Hematol. 2013 Jun;41(6):518-529.e5. doi: 10.1016/j.exphem.2013.02.006. Epub 2013 Feb 19.

DOI:10.1016/j.exphem.2013.02.006
PMID:23435313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3718276/
Abstract

Hoxa9 is expressed in hematopoietic stem and progenitor cells, although this expression is usually diminished as these cells undergo differentiation. In addition, aberrant expression of Hoxa9 is strongly associated with both T cell and myeloid leukemia in mice and humans. Despite this strong association, enforced expression of Hoxa9 in murine bone marrow or thymus has only shown a modest ability to transform cells. To investigate this question, we used Vav regulatory elements to generate a transgenic mouse that targets Hoxa9 overexpression to all hematopoietic tissues. High-level expression of the Hoxa9 transgene in the hematopoietic compartment was associated with embryonic lethality, as no pups from founders that expressed high levels of the transgene were born live. However, offspring of an additional founder line, which expressed lower levels of Hoxa9, developed a precursor T cell lymphoblastic leukemia/lymphoma, accompanied by spontaneous Notch1 mutations. In contrast to most murine models of leukemia associated with Hoxa9 overexpression, the Vav-Hoxa9 mice did not overexpress other Hoxa cluster genes, mir196b (a microRNA that is embedded in the Hoxa locus), Meis1, or Pbx3. The Hoxa9 transgenic mouse reported in this study provides a suitable system for the study of Hoxa9 collaborators that drive myeloid and lymphoid malignant transformation.

摘要

Hoxa9 在造血干细胞和祖细胞中表达,尽管这种表达通常会随着这些细胞分化而减少。此外,Hoxa9 的异常表达与小鼠和人类的 T 细胞和髓性白血病密切相关。尽管存在这种强烈的关联,但强制表达 Hoxa9 在小鼠骨髓或胸腺中仅显示出适度的转化细胞能力。为了研究这个问题,我们使用 Vav 调节元件生成了一种转基因小鼠,该小鼠将 Hoxa9 的过表达靶向所有造血组织。造血系中 Hoxa9 转基因的高水平表达与胚胎致死性相关,因为没有从表达高水平转基因的创始人中出生的活产幼仔。然而,来自表达较低水平 Hoxa9 的另一个创始人系的后代发展为前体 T 细胞淋巴母细胞白血病/淋巴瘤,伴有自发的 Notch1 突变。与大多数与 Hoxa9 过表达相关的小鼠白血病模型不同,Vav-Hoxa9 小鼠没有过度表达其他 Hoxa 簇基因、mir196b(一种嵌入 Hoxa 基因座的 microRNA)、Meis1 或 Pbx3。本研究中报道的 Hoxa9 转基因小鼠为研究驱动髓性和淋巴性恶性转化的 Hoxa9 合作者提供了一个合适的系统。