Cooperation between somatic Ikaros and Notch1 mutations at the inception of T-ALL

被引:2
|
作者
Sontani, Yovina [1 ]
Chapman, Gavin [3 ,4 ]
Papathanasiou, Peter [2 ]
Dunwoodie, Sally [3 ,4 ,5 ]
Goodnow, Christopher C. [1 ]
Hoyne, Gerard F. [1 ]
机构
[1] Australian Natl Univ, John Curtin Sch Med Res, Dept Immunol, Canberra, ACT 2601, Australia
[2] Australian Natl Univ, Australian Phen Facil, Canberra, ACT 2601, Australia
[3] Victor Chang Cardiac Res Inst, Dev Biol Program, Sydney, NSW, Australia
[4] Univ New S Wales, St Vincents Clin Sch, Sydney, NSW, Australia
[5] Univ New S Wales, Sch Biotechnol & Biomol Sci, Sydney, NSW, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Ikaros; Leukemia; Notch; Thymocytes; T cell; ACUTE LYMPHOBLASTIC-LEUKEMIA; GAMMA-SECRETASE INHIBITORS; GENE-EXPRESSION; CELL LEUKEMIA; SIGNALING PATHWAY; ACTIVATION; EVENT; LEUKEMOGENESIS; MICE; MUTAGENESIS;
D O I
10.1016/j.leukres.2011.07.024
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To understand the interactions between Notch1 and Ikaros in the evolution of T cell acute lymphoblastic leukemia (T-ALL), we traced the evolution of T-ALL in mice with an inherited Ikaros mutation, Ikzf1(Plstc) which inactivates DNA binding. DNA-binding Ikaros repressed Notch1 response in transfected cell lines and in CD4(+)8(+) (DP) thymocytes from young pre-leukemic Ikzf1(Plstc) heterozygous mice. In DP thymocytes, a 50-1000 fold escalation in mRNA for Notch1 target genes Hes1 and Dtx1 preceded thymic lymphoma or leukemia and was closely correlated with the first detectable differentiation abnormalities, loss of heterozygosity (LOH) eliminating wild-type Ikzf1, and multiple missense and truncating Notch1 mutations. These findings illuminate the early stages of leukemogenesis by demonstrating progressive exaggeration of Notch1 responsiveness at the DP thymocyte stage brought about by multiple mutations acting in concert upon the Notch1 pathway. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1512 / 1519
页数:8
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