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Recombinant Human erythropoietin reduces viability of MCF-7 breast cancer cells from 3D culture without caspase activation

Recombinant human erythropoietin (rHuEPO) is the erythropoiesis-stimulating hormone that is being used concurrently with chemotherapeutic drugs in the treatment of anemia of cancer. The effect of rHuEPO on cancer cells in 3-dimensional (3D) cultures is not known. The objective of the study was to de...

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Autores principales: ShujaaEdin, Hareth Y., AL-Haj, Nagi A., Rasedee, Abdullah, Alitheen, Noorjahan Banu, Kadir, Arifah Abdul, How, Chee Wun, Rahman, Heshu Sulaiman, Abdullah, Al-Shwyeh Hussah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071958/
https://www.ncbi.nlm.nih.gov/pubmed/33935571
http://dx.doi.org/10.1016/j.sjbs.2021.01.059
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author ShujaaEdin, Hareth Y.
AL-Haj, Nagi A.
Rasedee, Abdullah
Alitheen, Noorjahan Banu
Kadir, Arifah Abdul
How, Chee Wun
Rahman, Heshu Sulaiman
Abdullah, Al-Shwyeh Hussah
author_facet ShujaaEdin, Hareth Y.
AL-Haj, Nagi A.
Rasedee, Abdullah
Alitheen, Noorjahan Banu
Kadir, Arifah Abdul
How, Chee Wun
Rahman, Heshu Sulaiman
Abdullah, Al-Shwyeh Hussah
author_sort ShujaaEdin, Hareth Y.
collection PubMed
description Recombinant human erythropoietin (rHuEPO) is the erythropoiesis-stimulating hormone that is being used concurrently with chemotherapeutic drugs in the treatment of anemia of cancer. The effect of rHuEPO on cancer cells in 3-dimensional (3D) cultures is not known. The objective of the study was to determine the effect of rHuEPO on the viability of MCF-7 breast cancer cells from 2-dimensional (2D) and 3D cell cultures. The monolayer MCF-7 cells from 2D culture and MCF-7 cell from 3D culture generated by ultra-low adhesive microplate technique, were treated with 0, 0.1, 10, 100 or 200 IU/mL rHuEPO for 24, 48 or 72 h. The effects of rHuEPO on MCF-7 cell viability and proliferation were determined using the (4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay (MTT), neutral red retention time (NRRT), trypan blue exclusion assay (TBE), DNA fragmentation, acridine orange/propidium iodide staining (AO/PI) assays. The MCF-7 cells for 3D culture were also subjected to caspase assays and cell cycle analysis using flow cytometry. rHuEPO appeared to have greater effect at lowering the viability of MCF-7 cells from 3D than 2D cultures. rHuEPO significantly (p < 0.05) decreased viability and down-regulated the caspase activities of 3D MCF-7 cells in dose- and time-dependent manner. The cell cycle analysis showed that rHuEPO caused MCF-7 cells to enter the subG0/G1 phase. Thus, the study suggests that rHuEPO has a cytostatic effect on the MCF-7 breast cancer cells from 3D culture.
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spelling pubmed-80719582021-04-29 Recombinant Human erythropoietin reduces viability of MCF-7 breast cancer cells from 3D culture without caspase activation ShujaaEdin, Hareth Y. AL-Haj, Nagi A. Rasedee, Abdullah Alitheen, Noorjahan Banu Kadir, Arifah Abdul How, Chee Wun Rahman, Heshu Sulaiman Abdullah, Al-Shwyeh Hussah Saudi J Biol Sci Original Article Recombinant human erythropoietin (rHuEPO) is the erythropoiesis-stimulating hormone that is being used concurrently with chemotherapeutic drugs in the treatment of anemia of cancer. The effect of rHuEPO on cancer cells in 3-dimensional (3D) cultures is not known. The objective of the study was to determine the effect of rHuEPO on the viability of MCF-7 breast cancer cells from 2-dimensional (2D) and 3D cell cultures. The monolayer MCF-7 cells from 2D culture and MCF-7 cell from 3D culture generated by ultra-low adhesive microplate technique, were treated with 0, 0.1, 10, 100 or 200 IU/mL rHuEPO for 24, 48 or 72 h. The effects of rHuEPO on MCF-7 cell viability and proliferation were determined using the (4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay (MTT), neutral red retention time (NRRT), trypan blue exclusion assay (TBE), DNA fragmentation, acridine orange/propidium iodide staining (AO/PI) assays. The MCF-7 cells for 3D culture were also subjected to caspase assays and cell cycle analysis using flow cytometry. rHuEPO appeared to have greater effect at lowering the viability of MCF-7 cells from 3D than 2D cultures. rHuEPO significantly (p < 0.05) decreased viability and down-regulated the caspase activities of 3D MCF-7 cells in dose- and time-dependent manner. The cell cycle analysis showed that rHuEPO caused MCF-7 cells to enter the subG0/G1 phase. Thus, the study suggests that rHuEPO has a cytostatic effect on the MCF-7 breast cancer cells from 3D culture. Elsevier 2021-04 2021-02-11 /pmc/articles/PMC8071958/ /pubmed/33935571 http://dx.doi.org/10.1016/j.sjbs.2021.01.059 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
ShujaaEdin, Hareth Y.
AL-Haj, Nagi A.
Rasedee, Abdullah
Alitheen, Noorjahan Banu
Kadir, Arifah Abdul
How, Chee Wun
Rahman, Heshu Sulaiman
Abdullah, Al-Shwyeh Hussah
Recombinant Human erythropoietin reduces viability of MCF-7 breast cancer cells from 3D culture without caspase activation
title Recombinant Human erythropoietin reduces viability of MCF-7 breast cancer cells from 3D culture without caspase activation
title_full Recombinant Human erythropoietin reduces viability of MCF-7 breast cancer cells from 3D culture without caspase activation
title_fullStr Recombinant Human erythropoietin reduces viability of MCF-7 breast cancer cells from 3D culture without caspase activation
title_full_unstemmed Recombinant Human erythropoietin reduces viability of MCF-7 breast cancer cells from 3D culture without caspase activation
title_short Recombinant Human erythropoietin reduces viability of MCF-7 breast cancer cells from 3D culture without caspase activation
title_sort recombinant human erythropoietin reduces viability of mcf-7 breast cancer cells from 3d culture without caspase activation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071958/
https://www.ncbi.nlm.nih.gov/pubmed/33935571
http://dx.doi.org/10.1016/j.sjbs.2021.01.059
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