Dimeric bisbenzimidazoles DB(n) in combination with ionizing radiation decrease number and clonogenic activity of MCF-7 breast cancer stem cells

Purpose of the study was search for agents to eliminate the pool of cancer stem cells (CSCs) and increase their radiosensitivity among DNA minor groove binding ligands, synthetic dimeric bisbenzimidazoles of the DB(n) series, where n is the number of methylene groups in the linker connecting two bi...

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Main Authors: Irina A. Zamulaeva, Kristina A. Churyukina, Olga N. Matchuk, Alexander A. Ivanov, Vyacheslav O. Saburov, Alexei L. Zhuze
Format: Article
Language:English
Published: AIMS Press 2020-12-01
Series:AIMS Biophysics
Subjects:
Online Access:http://www.aimspress.com/article/doi/10.3934/biophy.2020024?viewType=HTML
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spelling doaj-726d57155fe54677a355492ed46558142020-12-04T02:03:27ZengAIMS PressAIMS Biophysics2377-90982020-12-017433936110.3934/biophy.2020024Dimeric bisbenzimidazoles DB(n) in combination with ionizing radiation decrease number and clonogenic activity of MCF-7 breast cancer stem cellsIrina A. Zamulaeva 0Kristina A. Churyukina 1Olga N. Matchuk2Alexander A. Ivanov3Vyacheslav O. Saburov4Alexei L. Zhuze 5 1. Department of Radiation Biochemistry, National Medical Research Radiological Center of the Ministry of Health of the Russian Federation, Obninsk, Russian Federation1. Department of Radiation Biochemistry, National Medical Research Radiological Center of the Ministry of Health of the Russian Federation, Obninsk, Russian Federation1. Department of Radiation Biochemistry, National Medical Research Radiological Center of the Ministry of Health of the Russian Federation, Obninsk, Russian Federation2. Laboratory of DNA-protein interactions, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russian Federation3. Department of Radiation Biophysics, National Medical Research Radiological Center of the Ministry of Health of the Russian Federation, Obninsk, Russian Federation2. Laboratory of DNA-protein interactions, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russian Federation Purpose of the study was search for agents to eliminate the pool of cancer stem cells (CSCs) and increase their radiosensitivity among DNA minor groove binding ligands, synthetic dimeric bisbenzimidazoles of the DB(n) series, where n is the number of methylene groups in the linker connecting two bisbenzimidazole residues (n = 1, 3, 5, 7, 9, 11). The investigation was concerned with MCF-7 breast cancer cells in vitro. Six compounds were synthesized, and their binding to cells and subcellular distribution were studied using flow cytometry and laser scanning microscopy. DB(5) and DB(7) demonstrated the highest binding and accumulation in cell nuclei and were selected for studying single and combined effects with γ-radiation at a dose of 4 Gy on number, clonogenic activity of CSCs and expression of vimentin, one of the major markers of epithelial to mesenchymal transition (EMT). Radiation exposure of MCF-7 cells increased the relative and absolute numbers of CD44<sup>+</sup>СD24<sup>−/low</sup> CSCs by a factor of 1.7 (р = 0.04) and 1.6 (р = 0.008), respectively, compared with the control. The combined exposure to DB(5) or DB(7) and γ-radiation led to a considerable reduction of CSC pool compared to control and single irradiation. Particularly, the CSC absolute number decreased by a factor of 16.6 and 14.1, respectively, after combined exposure compared to the radiation alone (р = 0.006 in both cases). The combined effects on the clonogenic activity were synergistic in case of CSCs, and additive or subadditive in case of non-CSCs. The combined exposure to DB(5) or DB(7) and γ-radiation resulted in inhibiting the radiation-induced EMT. Thus, DB(5, 7) were capable of removing the stimulating effect of γ-radiation on the CSC population. The suppression of radiation-induced EMT under the influence of these compounds caused a considerable reduction of CSC pool compared to both radiation and control.http://www.aimspress.com/article/doi/10.3934/biophy.2020024?viewType=HTMLcancer stem cellsdimeric bisbenzimidazolesionizing radiationcombined effectflow cytometry
collection DOAJ
language English
format Article
sources DOAJ
author Irina A. Zamulaeva
Kristina A. Churyukina
Olga N. Matchuk
Alexander A. Ivanov
Vyacheslav O. Saburov
Alexei L. Zhuze
spellingShingle Irina A. Zamulaeva
Kristina A. Churyukina
Olga N. Matchuk
Alexander A. Ivanov
Vyacheslav O. Saburov
Alexei L. Zhuze
Dimeric bisbenzimidazoles DB(n) in combination with ionizing radiation decrease number and clonogenic activity of MCF-7 breast cancer stem cells
AIMS Biophysics
cancer stem cells
dimeric bisbenzimidazoles
ionizing radiation
combined effect
flow cytometry
author_facet Irina A. Zamulaeva
Kristina A. Churyukina
Olga N. Matchuk
Alexander A. Ivanov
Vyacheslav O. Saburov
Alexei L. Zhuze
author_sort Irina A. Zamulaeva
title Dimeric bisbenzimidazoles DB(n) in combination with ionizing radiation decrease number and clonogenic activity of MCF-7 breast cancer stem cells
title_short Dimeric bisbenzimidazoles DB(n) in combination with ionizing radiation decrease number and clonogenic activity of MCF-7 breast cancer stem cells
title_full Dimeric bisbenzimidazoles DB(n) in combination with ionizing radiation decrease number and clonogenic activity of MCF-7 breast cancer stem cells
title_fullStr Dimeric bisbenzimidazoles DB(n) in combination with ionizing radiation decrease number and clonogenic activity of MCF-7 breast cancer stem cells
title_full_unstemmed Dimeric bisbenzimidazoles DB(n) in combination with ionizing radiation decrease number and clonogenic activity of MCF-7 breast cancer stem cells
title_sort dimeric bisbenzimidazoles db(n) in combination with ionizing radiation decrease number and clonogenic activity of mcf-7 breast cancer stem cells
publisher AIMS Press
series AIMS Biophysics
issn 2377-9098
publishDate 2020-12-01
description Purpose of the study was search for agents to eliminate the pool of cancer stem cells (CSCs) and increase their radiosensitivity among DNA minor groove binding ligands, synthetic dimeric bisbenzimidazoles of the DB(n) series, where n is the number of methylene groups in the linker connecting two bisbenzimidazole residues (n = 1, 3, 5, 7, 9, 11). The investigation was concerned with MCF-7 breast cancer cells in vitro. Six compounds were synthesized, and their binding to cells and subcellular distribution were studied using flow cytometry and laser scanning microscopy. DB(5) and DB(7) demonstrated the highest binding and accumulation in cell nuclei and were selected for studying single and combined effects with γ-radiation at a dose of 4 Gy on number, clonogenic activity of CSCs and expression of vimentin, one of the major markers of epithelial to mesenchymal transition (EMT). Radiation exposure of MCF-7 cells increased the relative and absolute numbers of CD44<sup>+</sup>СD24<sup>−/low</sup> CSCs by a factor of 1.7 (р = 0.04) and 1.6 (р = 0.008), respectively, compared with the control. The combined exposure to DB(5) or DB(7) and γ-radiation led to a considerable reduction of CSC pool compared to control and single irradiation. Particularly, the CSC absolute number decreased by a factor of 16.6 and 14.1, respectively, after combined exposure compared to the radiation alone (р = 0.006 in both cases). The combined effects on the clonogenic activity were synergistic in case of CSCs, and additive or subadditive in case of non-CSCs. The combined exposure to DB(5) or DB(7) and γ-radiation resulted in inhibiting the radiation-induced EMT. Thus, DB(5, 7) were capable of removing the stimulating effect of γ-radiation on the CSC population. The suppression of radiation-induced EMT under the influence of these compounds caused a considerable reduction of CSC pool compared to both radiation and control.
topic cancer stem cells
dimeric bisbenzimidazoles
ionizing radiation
combined effect
flow cytometry
url http://www.aimspress.com/article/doi/10.3934/biophy.2020024?viewType=HTML
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