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Investigation of the cytotoxicity of bioinspired coumarin analogues towards human breast cancer cells

ABSTRACT: Coumarins possess a wide array of therapeutic capabilities, but often with unclear mechanism of action. We tested a small library of 18 coumarin derivatives against human invasive breast ductal carcinoma cells with the capacity of each compound to inhibit cell proliferation scored, and the...

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Autores principales: Gkionis, Leonidas, Kavetsou, Eleni, Kalospyros, Alexandros, Manousakis, Dimitris, Garzon Sanz, Miguel, Butterworth, Sam, Detsi, Anastasia, Tirella, Annalisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870773/
https://www.ncbi.nlm.nih.gov/pubmed/32328962
http://dx.doi.org/10.1007/s11030-020-10082-6
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author Gkionis, Leonidas
Kavetsou, Eleni
Kalospyros, Alexandros
Manousakis, Dimitris
Garzon Sanz, Miguel
Butterworth, Sam
Detsi, Anastasia
Tirella, Annalisa
author_facet Gkionis, Leonidas
Kavetsou, Eleni
Kalospyros, Alexandros
Manousakis, Dimitris
Garzon Sanz, Miguel
Butterworth, Sam
Detsi, Anastasia
Tirella, Annalisa
author_sort Gkionis, Leonidas
collection PubMed
description ABSTRACT: Coumarins possess a wide array of therapeutic capabilities, but often with unclear mechanism of action. We tested a small library of 18 coumarin derivatives against human invasive breast ductal carcinoma cells with the capacity of each compound to inhibit cell proliferation scored, and the most potent coumarin analogues selected for further studies. Interestingly, the presence of two prenyloxy groups (5,7-diprenyloxy-4-methyl-coumarin, 4g) or the presence of octyloxy substituent (coumarin 4d) was found to increase the potency of compounds in breast cancer cells, but not against healthy human fibroblasts. The activity of potent compounds on breast cancer cells cultured more similarly to the conditions of the tumour microenvironment was also investigated, and increased toxicity was observed. Results suggest that tested coumarin derivatives could potentially reduce the growth of tumour mass. Moreover, their use as (combination) therapy in cancer treatment might have the potential of causing limited side effects. GRAPHIC ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11030-020-10082-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-78707732021-02-16 Investigation of the cytotoxicity of bioinspired coumarin analogues towards human breast cancer cells Gkionis, Leonidas Kavetsou, Eleni Kalospyros, Alexandros Manousakis, Dimitris Garzon Sanz, Miguel Butterworth, Sam Detsi, Anastasia Tirella, Annalisa Mol Divers Original Article ABSTRACT: Coumarins possess a wide array of therapeutic capabilities, but often with unclear mechanism of action. We tested a small library of 18 coumarin derivatives against human invasive breast ductal carcinoma cells with the capacity of each compound to inhibit cell proliferation scored, and the most potent coumarin analogues selected for further studies. Interestingly, the presence of two prenyloxy groups (5,7-diprenyloxy-4-methyl-coumarin, 4g) or the presence of octyloxy substituent (coumarin 4d) was found to increase the potency of compounds in breast cancer cells, but not against healthy human fibroblasts. The activity of potent compounds on breast cancer cells cultured more similarly to the conditions of the tumour microenvironment was also investigated, and increased toxicity was observed. Results suggest that tested coumarin derivatives could potentially reduce the growth of tumour mass. Moreover, their use as (combination) therapy in cancer treatment might have the potential of causing limited side effects. GRAPHIC ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11030-020-10082-6) contains supplementary material, which is available to authorized users. Springer International Publishing 2020-04-23 2021 /pmc/articles/PMC7870773/ /pubmed/32328962 http://dx.doi.org/10.1007/s11030-020-10082-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Gkionis, Leonidas
Kavetsou, Eleni
Kalospyros, Alexandros
Manousakis, Dimitris
Garzon Sanz, Miguel
Butterworth, Sam
Detsi, Anastasia
Tirella, Annalisa
Investigation of the cytotoxicity of bioinspired coumarin analogues towards human breast cancer cells
title Investigation of the cytotoxicity of bioinspired coumarin analogues towards human breast cancer cells
title_full Investigation of the cytotoxicity of bioinspired coumarin analogues towards human breast cancer cells
title_fullStr Investigation of the cytotoxicity of bioinspired coumarin analogues towards human breast cancer cells
title_full_unstemmed Investigation of the cytotoxicity of bioinspired coumarin analogues towards human breast cancer cells
title_short Investigation of the cytotoxicity of bioinspired coumarin analogues towards human breast cancer cells
title_sort investigation of the cytotoxicity of bioinspired coumarin analogues towards human breast cancer cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870773/
https://www.ncbi.nlm.nih.gov/pubmed/32328962
http://dx.doi.org/10.1007/s11030-020-10082-6
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