MLL-AF9驱动的侵袭性白血病。

Molecular & cellular oncology Pub Date : 2017-10-23 eCollection Date: 2018-01-01 DOI:10.1080/23723556.2016.1241854
Vaia Stavropoulou, Antoine H F M Peters, Juerg Schwaller
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引用次数: 10

摘要

我们最近发现细胞起源影响急性髓性白血病(AML)的侵袭性和表型。使用多西环素(DOX)调节的小鼠模型(iMLL-AF9)在体内各种造血室中直接诱导MLL-AF9融合导致侵袭性化疗耐药AML,表达几种已知参与实体癌上皮到间质转化(EMT)的基因。其中许多基因在迁移和侵袭中发挥重要作用,并与AML患者较差的总生存率显著相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Aggressive leukemia driven by MLL-AF9.

Aggressive leukemia driven by MLL-AF9.

We recently showed that cellular origin impacts the aggressiveness and the phenotype of acute myeloid leukemia (AML). Direct induction of the MLL-AF9 fusion in various hematopoietic compartments in vivo using a doxycycline (DOX) regulated mouse model (iMLL-AF9) led to an invasive chemoresistant AML expressing several genes known to be involved in epithelial to mesenchymal transition (EMT) in solid cancers. Many of these genes play important roles in migration and invasion and are significantly associated with poor overall survival in AML patients.

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