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VENTX诱导原始红细胞扩增,并促进小鼠急性髓系白血病的发展。

VENTX induces expansion of primitive erythroid cells and contributes to the development of acute myeloid leukemia in mice.

作者信息

Gentner Eva, Vegi Naidu M, Mulaw Medhanie A, Mandal Tamoghna, Bamezai Shiva, Claus Rainer, Tasdogan Alpaslan, Quintanilla-Martinez Leticia, Grunenberg Alexander, Döhner Konstanze, Döhner Hartmut, Bullinger Lars, Haferlach Torsten, Buske Christian, Rawat Vijay P S, Feuring-Buske Michaela

机构信息

Institute of Experimental Cancer Research, CCC and University Hospital of Ulm, 89081 Ulm, Germany.

Department of Internal Medicine I, University Hospital Freiburg, 79106 Freiburg, Germany.

出版信息

Oncotarget. 2016 Dec 27;7(52):86889-86901. doi: 10.18632/oncotarget.13563.

Abstract

Homeobox genes are key regulators in normal and malignant hematopoiesis. The human Vent-like homeobox gene VENTX, a putative homolog of the Xenopus laevis Xvent-2 gene, was shown to be highly expressed in normal myeloid cells and in patients with acute myeloid leukemia. We now demonstrate that constitutive expression of VENTX suppresses expression of genes responsible for terminal erythroid differentiation in normal CD34+ stem and progenitor cells. Transplantation of bone marrow progenitor cells retrovirally engineered to express VENTX caused massive expansion of primitive erythroid cells and partly acute erythroleukemia in transplanted mice. The leukemogenic potential of VENTX was confirmed in the AML1-ETO transplantation model, as in contrast to AML1-ETO alone co-expression of AML1-ETO and VENTX induced acute myeloid leukemia, partly expressing erythroid markers, in all transplanted mice. VENTX was highly expressed in patients with primary human erythroleukemias and knockdown of VENTX in the erythroleukemic HEL cell line significantly blocked cell growth. In summary, these data indicate that VENTX is able to perturb erythroid differentiation and to contribute to myeloid leukemogenesis when co-expressed with appropriate AML oncogenes and point to its potential significance as a novel therapeutic target in AML.

摘要

同源框基因是正常和恶性造血过程中的关键调节因子。人类Vent样同源框基因VENTX是非洲爪蟾Xvent - 2基因的假定同源物,已证实在正常髓系细胞和急性髓系白血病患者中高表达。我们现在证明,VENTX的组成型表达会抑制正常CD34 + 干细胞和祖细胞中负责终末红系分化的基因的表达。逆转录病毒工程改造以表达VENTX的骨髓祖细胞移植导致移植小鼠体内原始红系细胞大量扩增,并部分引发急性红白血病。VENTX的致白血病潜能在AML1 - ETO移植模型中得到证实,因为与单独的AML1 - ETO相比,AML1 - ETO和VENTX的共表达在所有移植小鼠中诱导了急性髓系白血病,部分表达红系标志物。VENTX在原发性人类红白血病患者中高表达,并且在红白血病HEL细胞系中敲低VENTX可显著阻断细胞生长。总之,这些数据表明,VENTX能够干扰红系分化,并且在与适当的AML癌基因共表达时有助于髓系白血病的发生,并指出其作为AML新型治疗靶点的潜在意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8513/5349961/2aaee61eff9c/oncotarget-07-86889-g002.jpg

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