The intensification of anticancer activity of LFM-A13 by erythropoietin as a possible option for inhibition of breast cancer
Recombinant human erythropoietin (Epo) is an effective and convenient treatment for cancer-related anaemia. In our study for the first time, we evaluated the effect of simultaneous use of Epo and Bruton’s tyrosine kinase (BTK) inhibitor LFM-A13 on the viability and tumour development of breast cance...
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doaj-418377d1f791473ea76404dcb6f5a02c2021-07-15T13:10:33ZengTaylor & Francis GroupJournal of Enzyme Inhibition and Medicinal Chemistry1475-63661475-63742020-01-013511697171110.1080/14756366.2020.18187381818738The intensification of anticancer activity of LFM-A13 by erythropoietin as a possible option for inhibition of breast cancerDariusz Rozkiewicz0Justyna Magdalena Hermanowicz1Anna Tankiewicz-Kwedlo2Beata Sieklucka3Krystyna Pawlak4Robert Czarnomysy5Krzysztof Bielawski6Arkadiusz Surazynski7Joanna Kalafut8Alicja Przybyszewska9Mariusz Koda10Katarzyna Jakubowska11Adolfo Rivero-Muller12Dariusz Pawlak13Department of Pharmacodynamics, Medical University of BialystokDepartment of Pharmacodynamics, Medical University of BialystokDepartment of Monitored Pharmacotherapy, Medical University of BialystokDepartment of Pharmacodynamics, Medical University of BialystokDepartment of Monitored Pharmacotherapy, Medical University of BialystokDepartment of Synthesis and Technology of Drugs, Medical University of BialystokDepartment of Synthesis and Technology of Drugs, Medical University of BialystokDepartment of Medicinal Chemistry, Medical University of BialystokDepartment of Biochemistry and Molecular Biology, Medical University of LublinDepartment of Biochemistry and Molecular Biology, Medical University of LublinDepartment of General Pathomorphology, Medical University of BialystokDepartment of Pathomorphology, Comprehensive Cancer CenterDepartment of Biochemistry and Molecular Biology, Medical University of LublinDepartment of Pharmacodynamics, Medical University of BialystokRecombinant human erythropoietin (Epo) is an effective and convenient treatment for cancer-related anaemia. In our study for the first time, we evaluated the effect of simultaneous use of Epo and Bruton’s tyrosine kinase (BTK) inhibitor LFM-A13 on the viability and tumour development of breast cancer cells. The results demonstrated that Epo significantly intensifies the anticancer activity of LFM-A13 in MCF-7 and MDA-MB-231. The featured therapeutic scheme efficiently blocked the tumour development in zebrafish experimental cancer model. Epo and LFM-A13 administered together resulted in effective cell killing, accompanied by attenuation of the BTK signalling pathways, loss of mitochondrial membrane potential (MMP), accumulation of apoptotic breast cancer cells with externalised PS, a slight increase in phase G0/G1 and a reduction in cyclin D1 expression. Simultaneous use of Epo with LFM-A13 inhibited early stages of tumour progression. This therapeutic scheme may be rationale for further possible research.http://dx.doi.org/10.1080/14756366.2020.1818738erythropoietinlfm-a13bruton’s tyrosine kinasebreast cancerzebrafish |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Dariusz Rozkiewicz Justyna Magdalena Hermanowicz Anna Tankiewicz-Kwedlo Beata Sieklucka Krystyna Pawlak Robert Czarnomysy Krzysztof Bielawski Arkadiusz Surazynski Joanna Kalafut Alicja Przybyszewska Mariusz Koda Katarzyna Jakubowska Adolfo Rivero-Muller Dariusz Pawlak |
spellingShingle |
Dariusz Rozkiewicz Justyna Magdalena Hermanowicz Anna Tankiewicz-Kwedlo Beata Sieklucka Krystyna Pawlak Robert Czarnomysy Krzysztof Bielawski Arkadiusz Surazynski Joanna Kalafut Alicja Przybyszewska Mariusz Koda Katarzyna Jakubowska Adolfo Rivero-Muller Dariusz Pawlak The intensification of anticancer activity of LFM-A13 by erythropoietin as a possible option for inhibition of breast cancer Journal of Enzyme Inhibition and Medicinal Chemistry erythropoietin lfm-a13 bruton’s tyrosine kinase breast cancer zebrafish |
author_facet |
Dariusz Rozkiewicz Justyna Magdalena Hermanowicz Anna Tankiewicz-Kwedlo Beata Sieklucka Krystyna Pawlak Robert Czarnomysy Krzysztof Bielawski Arkadiusz Surazynski Joanna Kalafut Alicja Przybyszewska Mariusz Koda Katarzyna Jakubowska Adolfo Rivero-Muller Dariusz Pawlak |
author_sort |
Dariusz Rozkiewicz |
title |
The intensification of anticancer activity of LFM-A13 by erythropoietin as a possible option for inhibition of breast cancer |
title_short |
The intensification of anticancer activity of LFM-A13 by erythropoietin as a possible option for inhibition of breast cancer |
title_full |
The intensification of anticancer activity of LFM-A13 by erythropoietin as a possible option for inhibition of breast cancer |
title_fullStr |
The intensification of anticancer activity of LFM-A13 by erythropoietin as a possible option for inhibition of breast cancer |
title_full_unstemmed |
The intensification of anticancer activity of LFM-A13 by erythropoietin as a possible option for inhibition of breast cancer |
title_sort |
intensification of anticancer activity of lfm-a13 by erythropoietin as a possible option for inhibition of breast cancer |
publisher |
Taylor & Francis Group |
series |
Journal of Enzyme Inhibition and Medicinal Chemistry |
issn |
1475-6366 1475-6374 |
publishDate |
2020-01-01 |
description |
Recombinant human erythropoietin (Epo) is an effective and convenient treatment for cancer-related anaemia. In our study for the first time, we evaluated the effect of simultaneous use of Epo and Bruton’s tyrosine kinase (BTK) inhibitor LFM-A13 on the viability and tumour development of breast cancer cells. The results demonstrated that Epo significantly intensifies the anticancer activity of LFM-A13 in MCF-7 and MDA-MB-231. The featured therapeutic scheme efficiently blocked the tumour development in zebrafish experimental cancer model. Epo and LFM-A13 administered together resulted in effective cell killing, accompanied by attenuation of the BTK signalling pathways, loss of mitochondrial membrane potential (MMP), accumulation of apoptotic breast cancer cells with externalised PS, a slight increase in phase G0/G1 and a reduction in cyclin D1 expression. Simultaneous use of Epo with LFM-A13 inhibited early stages of tumour progression. This therapeutic scheme may be rationale for further possible research. |
topic |
erythropoietin lfm-a13 bruton’s tyrosine kinase breast cancer zebrafish |
url |
http://dx.doi.org/10.1080/14756366.2020.1818738 |
work_keys_str_mv |
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