Suppression of chronic lymphocytic leukemia progression by CXCR4 inhibitor WZ811

被引:1
作者
Li, Shi Hui [1 ]
Dong, Wen Chuan [1 ]
Fan, Li [1 ]
Wang, Guang Sheng [1 ]
机构
[1] Aviat Gen Hosp, Dept Oncol, 3 Beiyuan Rd, Beijing 100012, Peoples R China
来源
AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH | 2016年 / 8卷 / 09期
关键词
Chronic lymphocytic leukemia; CXCR4; WZ811; docetaxel; BREAST-CANCER CELLS; CHEMOKINE RECEPTOR; IN-VITRO; GROWTH-FACTOR; MIGRATION; MICROENVIRONMENT; PROLIFERATION; EXPRESSION; APOPTOSIS; INVASION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CXCR4 is a chemokine and chemokine receptor pair playing critical roles in tumorigenesis. Overexpression of C-X-C chemokine receptor type 4 (CXCR4) is a hallmark of many hematological malignancies including acute myeloid leukemia, chronic lymphocytic leukemia and non-Hodgkin's lymphoma, and generally correlates with a poor prognosis. A highly potent competitive antagonist of CXCR4, WZ811, recently has been identified with suppression of cancer cells aggressive in a variety of cancers. However, the effects of WZ811 on chronic lymphocytic leukemia cells have not yet been defined. The effect of WZ811 on chronic lymphocytic leukemia cells TF-1 and UT-7 cells in proliferation, colony formation, and cell migration in vitro were measured respectively. Decreased in cell viability, colony formation, migration, and survival with cell cycle arrest and higher sensitivity to docetaxel in vitro was observed upon WZ811 treatment. In mouse xenograft models developed with human leukemia cells, WZ811 exhibited tumor growth inhibition. Collectively, we have demonstrated that CXCR4 inhibition by WZ811 has the potential for the treatment of human hematological malignancies. This study demonstrated that WZ811 may be a novel approach in the treatment of chronic lymphocytic leukemia.
引用
收藏
页码:3812 / 3821
页数:10
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