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VEGFC 抗体疗法促进 AML 分化。

VEGFC Antibody Therapy Drives Differentiation of AML.

机构信息

Division of Pediatric Oncology/Hematology, Department of Pediatrics, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

Laboratory for Disease Mechanisms in Cancer, Department of Oncology, KU Leuven, University of Leuven, Leuven Cancer Institute (LKI), Leuven, Belgium.

出版信息

Cancer Res. 2018 Oct 15;78(20):5940-5948. doi: 10.1158/0008-5472.CAN-18-0250. Epub 2018 Sep 5.

Abstract

High expression of VEGFC predicts adverse prognosis in acute myeloid leukemia (AML). We therefore explored VEGFC-targeting efficacy as an AML therapy using a VEGFC mAb. VEGFC antibody therapy enforced myelocytic differentiation of clonal CD34 AML blasts. Treatment of CD34 AML blasts with the antibody reduced expansion potential by 30% to 50% and enhanced differentiation via FOXO3A suppression and inhibition of MAPK/ERK proliferative signals. VEGFC antibody therapy also accelerated leukemia cell differentiation in a systemic humanized AML mouse model. Collectively, these results define a regulatory function of VEGFC in CD34 AML cell fate decisions via FOXO3A and serve as a new potential differentiation therapy for patients with AML. These findings reveal VEGFC targeting as a promising new differentiation therapy in AML. .

摘要

VEGFC 的高表达预示着急性髓系白血病(AML)的不良预后。因此,我们探索了 VEGFC 单克隆抗体作为 AML 治疗的靶向疗效。VEGFC 抗体治疗可促进克隆性 CD34 AML 白血病细胞向髓系分化。该抗体治疗可使 CD34 AML 白血病细胞的扩增潜能降低 30%至 50%,并通过抑制 FOXO3A 和 MAPK/ERK 增殖信号促进分化。VEGFC 抗体治疗还可在全身性人源化 AML 小鼠模型中加速白血病细胞分化。总之,这些结果定义了 VEGFC 通过 FOXO3A 对 CD34 AML 细胞命运决定的调节功能,并为 AML 患者提供了一种新的潜在分化治疗方法。这些发现表明,VEGFC 靶向治疗是 AML 中一种有前途的新分化治疗方法。

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