Atorvastatin and Nitrofurantoin Repurposed in the Context of Breast Cancer and Neuroblastoma Cells
Chemotherapy still plays a central role in the treatment of cancer. However, it is often accompanied by off-target effects that result in severe side-effects and development of drug resistance. The aim of this work was to study the efficacy of different repurposed drugs on the viability of MCF-7 and...
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MDPI AG
2023-03-01
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Online Access: | https://www.mdpi.com/2227-9059/11/3/903 |
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author | Catarina Moura Ana Salomé Correia Mariana Pereira Eduarda Ribeiro Joana Santos Nuno Vale |
author_facet | Catarina Moura Ana Salomé Correia Mariana Pereira Eduarda Ribeiro Joana Santos Nuno Vale |
author_sort | Catarina Moura |
collection | DOAJ |
description | Chemotherapy still plays a central role in the treatment of cancer. However, it is often accompanied by off-target effects that result in severe side-effects and development of drug resistance. The aim of this work was to study the efficacy of different repurposed drugs on the viability of MCF-7 and SH-SY5Y breast cancer and neuroblastoma cells, respectively. In addition, combinations of these repurposed drugs with a classical chemotherapeutic drug (doxorubicin) were also carried out. The cytotoxic effects of the repurposed drugs were evaluated individually and in combination in both cancer cell lines, assessed by MTT assays and morphological evaluation of the cells. The results demonstrated that atorvastatin reduced the viability of both cell lines. However, nitrofurantoin was able to induce cytotoxic effects in MCF-7 cells, but not in SH-SY5Y cells. The combinations of the repurposed drugs with doxorubicin induced a higher inhibition on cell viability than the repurposed drugs individually. The combination of the two repurposed drugs demonstrated that they potentiate each other. Synergism studies revealed that the combination of doxorubicin with the two repurposed drugs was more effective in SH-SY5Y cells, compared to MCF-7 cells. Taken together, our preliminary study highlights the potential use of atorvastatin and nitrofurantoin in the context of breast cancer and neuroblastoma. |
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issn | 2227-9059 |
language | English |
last_indexed | 2024-03-11T06:53:43Z |
publishDate | 2023-03-01 |
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spelling | doaj.art-93b4a89a71e848ac86bc86388c5ec6d22023-11-17T09:47:18ZengMDPI AGBiomedicines2227-90592023-03-0111390310.3390/biomedicines11030903Atorvastatin and Nitrofurantoin Repurposed in the Context of Breast Cancer and Neuroblastoma CellsCatarina Moura0Ana Salomé Correia1Mariana Pereira2Eduarda Ribeiro3Joana Santos4Nuno Vale5OncoPharma Research Group, Center for Health Technology and Services Research (CINTESIS), Rua Doutor Plácido da Costa, 4200-450 Porto, PortugalOncoPharma Research Group, Center for Health Technology and Services Research (CINTESIS), Rua Doutor Plácido da Costa, 4200-450 Porto, PortugalOncoPharma Research Group, Center for Health Technology and Services Research (CINTESIS), Rua Doutor Plácido da Costa, 4200-450 Porto, PortugalOncoPharma Research Group, Center for Health Technology and Services Research (CINTESIS), Rua Doutor Plácido da Costa, 4200-450 Porto, PortugalOncoPharma Research Group, Center for Health Technology and Services Research (CINTESIS), Rua Doutor Plácido da Costa, 4200-450 Porto, PortugalOncoPharma Research Group, Center for Health Technology and Services Research (CINTESIS), Rua Doutor Plácido da Costa, 4200-450 Porto, PortugalChemotherapy still plays a central role in the treatment of cancer. However, it is often accompanied by off-target effects that result in severe side-effects and development of drug resistance. The aim of this work was to study the efficacy of different repurposed drugs on the viability of MCF-7 and SH-SY5Y breast cancer and neuroblastoma cells, respectively. In addition, combinations of these repurposed drugs with a classical chemotherapeutic drug (doxorubicin) were also carried out. The cytotoxic effects of the repurposed drugs were evaluated individually and in combination in both cancer cell lines, assessed by MTT assays and morphological evaluation of the cells. The results demonstrated that atorvastatin reduced the viability of both cell lines. However, nitrofurantoin was able to induce cytotoxic effects in MCF-7 cells, but not in SH-SY5Y cells. The combinations of the repurposed drugs with doxorubicin induced a higher inhibition on cell viability than the repurposed drugs individually. The combination of the two repurposed drugs demonstrated that they potentiate each other. Synergism studies revealed that the combination of doxorubicin with the two repurposed drugs was more effective in SH-SY5Y cells, compared to MCF-7 cells. Taken together, our preliminary study highlights the potential use of atorvastatin and nitrofurantoin in the context of breast cancer and neuroblastoma.https://www.mdpi.com/2227-9059/11/3/903doxorubicindrug combinationdrug repurposingMCF-7 cellsSH-SY5Y cellsatorvastatin |
spellingShingle | Catarina Moura Ana Salomé Correia Mariana Pereira Eduarda Ribeiro Joana Santos Nuno Vale Atorvastatin and Nitrofurantoin Repurposed in the Context of Breast Cancer and Neuroblastoma Cells Biomedicines doxorubicin drug combination drug repurposing MCF-7 cells SH-SY5Y cells atorvastatin |
title | Atorvastatin and Nitrofurantoin Repurposed in the Context of Breast Cancer and Neuroblastoma Cells |
title_full | Atorvastatin and Nitrofurantoin Repurposed in the Context of Breast Cancer and Neuroblastoma Cells |
title_fullStr | Atorvastatin and Nitrofurantoin Repurposed in the Context of Breast Cancer and Neuroblastoma Cells |
title_full_unstemmed | Atorvastatin and Nitrofurantoin Repurposed in the Context of Breast Cancer and Neuroblastoma Cells |
title_short | Atorvastatin and Nitrofurantoin Repurposed in the Context of Breast Cancer and Neuroblastoma Cells |
title_sort | atorvastatin and nitrofurantoin repurposed in the context of breast cancer and neuroblastoma cells |
topic | doxorubicin drug combination drug repurposing MCF-7 cells SH-SY5Y cells atorvastatin |
url | https://www.mdpi.com/2227-9059/11/3/903 |
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