Cell aggregation increases drug resistance of acute myeloid leukemia cells

被引:0
|
作者
Fadeev R.S. [1 ]
Solovieva M.E. [1 ]
Slyadovskiy D.A. [3 ]
Zakharov S.G. [4 ]
Fadeeva I.S. [1 ,2 ]
Senotov A.S. [5 ]
Dolgikh N.V. [1 ,2 ]
Golenkov A.K. [4 ]
Akatov V.S. [1 ,2 ]
机构
[1] Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences, Pushchino, Moscow oblast
[2] Pushchino State Natural Science Institute, Pushchino, Moscow oblast
[3] Nizhni Novgorod Lobachevsky National Research University, Nizhni Novgorod
[4] Vladimirsky Moscow Regional Research Clinical Institute (MONIKI), Moscow
[5] Saratov Medical Center of the FMBA of Russia, Balakovo, Saratov oblast
基金
俄罗斯基础研究基金会;
关键词
acute myeloid leukemia; drug resistance; intercellular adhesion; multicellular aggregates;
D O I
10.1134/S1990747815020063
中图分类号
学科分类号
摘要
One of the major causes of low efficiency of the therapy for acute myeloid leukemia is drug resistance of leukemic cells. Microenvironment plays a key role in formation of the phenotype of leukemic cell drug resistance. Investigation of the mechanisms of microenvironment-mediated drug resistance is important to identify novel pharmacological targets for the acute myeloid leukemia therapy. We studied the role of cell aggregation in the drug resistance of leukemic cells. We showed the increased resistance of acute myeloid leukemia cells THP-1 to bortezomib, doxorubicin and fludarabine in multicellular aggregates. In the multicellular aggregates of THP-1 with the higher drug resistance, cell proliferation activity did not change, while the intracellular level of anti-apoptotic protein Bcl-2 increased. Inhibition of the aggregation of THP-1 cells prevented drug resistance. This work demonstrates the involvement of cell aggregation in the formation of drug resistance phenotype in leukemic cells. © 2015, Pleiades Publishing, Ltd.
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页码:135 / 143
页数:8
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