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ETV6-NCOA2 fusion induces T/myeloid mixed-phenotype leukemia through transformation of nonthymic hematopoietic progenitor cells.ETV6-NCOA2 融合通过转化非胸腺造血祖细胞诱导 T/髓系混合表型白血病。
Blood. 2022 Jan 20;139(3):399-412. doi: 10.1182/blood.2020010405.
2
How transcription factors drive choice of the T cell fate.转录因子如何驱动 T 细胞命运的选择。
Nat Rev Immunol. 2021 Mar;21(3):162-176. doi: 10.1038/s41577-020-00426-6. Epub 2020 Sep 11.
3
Optimal therapeutic strategies for mixed phenotype acute leukemia.混合表型急性白血病的最佳治疗策略。
Curr Opin Hematol. 2020 Mar;27(2):95-102. doi: 10.1097/MOH.0000000000000570.
4
The genetic basis and cell of origin of mixed phenotype acute leukaemia.混合表型急性白血病的遗传基础和细胞起源。
Nature. 2018 Oct;562(7727):373-379. doi: 10.1038/s41586-018-0436-0. Epub 2018 Sep 12.
5
Integrative genomic analysis of adult mixed phenotype acute leukemia delineates lineage associated molecular subtypes.成人混合表型急性白血病的综合基因组分析描绘了与谱系相关的分子亚型。
Nat Commun. 2018 Jul 10;9(1):2670. doi: 10.1038/s41467-018-04924-z.
6
ETV6 mutations in early immature human T cell leukemias.早期未成熟人类 T 细胞白血病中的 ETV6 突变。
J Exp Med. 2011 Dec 19;208(13):2571-9. doi: 10.1084/jem.20112239. Epub 2011 Dec 12.
7
Integrated transcript and genome analyses reveal NKX2-1 and MEF2C as potential oncogenes in T cell acute lymphoblastic leukemia.综合转录组和基因组分析揭示 NKX2-1 和 MEF2C 是 T 细胞急性淋巴细胞白血病潜在的癌基因。
Cancer Cell. 2011 Apr 12;19(4):484-97. doi: 10.1016/j.ccr.2011.02.008.
8
Mixed-phenotype acute leukemia: clinical and laboratory features and outcome in 100 patients defined according to the WHO 2008 classification.混合表型急性白血病:根据 WHO 2008 分类定义的 100 例患者的临床和实验室特征及预后。
Blood. 2011 Mar 17;117(11):3163-71. doi: 10.1182/blood-2010-10-314682. Epub 2011 Jan 12.
9
Early T-cell precursor leukaemia: a subtype of very high-risk acute lymphoblastic leukaemia.早期T细胞前体白血病:一种极高危急性淋巴细胞白血病亚型。
Lancet Oncol. 2009 Feb;10(2):147-56. doi: 10.1016/S1470-2045(08)70314-0. Epub 2009 Jan 13.
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ETV6-NCOA2: a novel fusion gene in acute leukemia associated with coexpression of T-lymphoid and myeloid markers and frequent NOTCH1 mutations.ETV6-NCOA2:急性白血病中的一种新型融合基因,与T淋巴细胞和髓系标志物共表达及频繁的NOTCH1突变相关。
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T/myeloid MPAL: origin and pathogenesis.

作者信息

McCormack Matthew P

机构信息

Monash University.

出版信息

Blood. 2022 Jan 20;139(3):313-315. doi: 10.1182/blood.2021014129.

DOI:10.1182/blood.2021014129
PMID:35050331
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8777204/
Abstract
摘要