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The closely related rare and severe acute myeloid leukemias carrying EVI1 or PRDM16 rearrangements share singular biological features.

作者信息

Eveillard Marion, Delaunay Jacques, Richebourg Steven, Lodé Laurence, Garand Richard, Wuillème Soraya, Duhoux François, Antoine-Poirel Hélène, Godon Catherine, Béné Marie C

机构信息

Hematology Laboratory, University Hospital, Nantes, France

Hematology Clinic, University Hospital, Nantes, France.

出版信息

Haematologica. 2015 Mar;100(3):e114-5. doi: 10.3324/haematol.2014.121079.

DOI:10.3324/haematol.2014.121079
PMID:25740106
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4349292/
Abstract
摘要

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The closely related rare and severe acute myeloid leukemias carrying EVI1 or PRDM16 rearrangements share singular biological features.携带EVI1或PRDM16重排的密切相关的罕见且严重的急性髓系白血病具有独特的生物学特征。
Haematologica. 2015 Mar;100(3):e114-5. doi: 10.3324/haematol.2014.121079.
2
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3
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Marked thrombocytosis and dysmegakaryopoiesis in acute myeloid leukemia with t(2;3)(p22;q26.2) and EVI1 rearrangement.伴有t(2;3)(p22;q26.2)和EVI1重排的急性髓系白血病中的显著血小板增多和巨核细胞生成异常。
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本文引用的文献

1
EVI1-rearranged acute myeloid leukemias are characterized by distinct molecular alterations.EVI1 重排急性髓系白血病的特征是明显的分子改变。
Blood. 2015 Jan 1;125(1):140-3. doi: 10.1182/blood-2014-07-591529. Epub 2014 Oct 20.
2
EVI1 overexpression is a poor prognostic factor in pediatric patients with mixed lineage leukemia-AF9 rearranged acute myeloid leukemia.EVI1过表达是混合谱系白血病-AF9重排急性髓系白血病患儿的不良预后因素。
Haematologica. 2014 Nov;99(11):e225-7. doi: 10.3324/haematol.2014.107128. Epub 2014 Jul 11.
3
A remote GATA2 hematopoietic enhancer drives leukemogenesis in inv(3)(q21;q26) by activating EVI1 expression.远程 GATA2 造血增强子通过激活 EVI1 表达驱动 inv(3)(q21;q26) 白血病的发生。
Cancer Cell. 2014 Apr 14;25(4):415-27. doi: 10.1016/j.ccr.2014.02.008. Epub 2014 Apr 3.
4
Complex or monosomal karyotype and not blast percentage is associated with poor survival in acute myeloid leukemia and myelodysplastic syndrome patients with inv(3)(q21q26.2)/t(3;3)(q21;q26.2): a Bone Marrow Pathology Group study.复杂或单体核型而非原始细胞百分比与急性髓系白血病和伴有inv(3)(q21q26.2)/t(3;3)(q21;q26.2)的骨髓增生异常综合征患者的不良生存相关：一项骨髓病理学组研究。
Haematologica. 2014 May;99(5):821-9. doi: 10.3324/haematol.2013.096420. Epub 2014 Jan 24.
5
Clinical, molecular, and prognostic significance of WHO type inv(3)(q21q26.2)/t(3;3)(q21;q26.2) and various other 3q abnormalities in acute myeloid leukemia.急性髓系白血病中 WHO 类型 inv(3)(q21q26.2)/t(3;3)(q21;q26.2) 和其他各种 3q 异常的临床、分子和预后意义。
J Clin Oncol. 2010 Aug 20;28(24):3890-8. doi: 10.1200/JCO.2010.29.2771. Epub 2010 Jul 26.
6
Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials.在英国医学研究理事会试验中治疗的 5876 例年轻成年患者中，对罕见重现染色体异常进行细胞遗传学分类的细化：确定其预后意义。
Blood. 2010 Jul 22;116(3):354-65. doi: 10.1182/blood-2009-11-254441. Epub 2010 Apr 12.
7
High EVI1 expression predicts outcome in younger adult patients with acute myeloid leukemia and is associated with distinct cytogenetic abnormalities.EVI1 高表达可预测年轻成人急性髓系白血病患者的预后，并与独特的细胞遗传学异常相关。
J Clin Oncol. 2010 Apr 20;28(12):2101-7. doi: 10.1200/JCO.2009.26.0646. Epub 2010 Mar 22.
8
EVI1 Impairs myelopoiesis by deregulation of PU.1 function.EVI1 通过失调 PU.1 功能损害骨髓生成。
Cancer Res. 2009 Feb 15;69(4):1633-42. doi: 10.1158/0008-5472.CAN-08-2562. Epub 2009 Feb 10.
9
The role of EVI1 in normal and leukemic cells.EVI1在正常细胞和白血病细胞中的作用。
Blood Cells Mol Dis. 2003 Sep-Oct;31(2):206-12. doi: 10.1016/s1079-9796(03)00159-1.
10
A novel gene, MEL1, mapped to 1p36.3 is highly homologous to the MDS1/EVI1 gene and is transcriptionally activated in t(1;3)(p36;q21)-positive leukemia cells.一个定位于1p36.3的新基因MEL1与MDS1/EVI1基因高度同源，且在t(1;3)(p36;q21)阳性白血病细胞中被转录激活。
Blood. 2000 Nov 1;96(9):3209-14.