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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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Detalles Bibliográficos
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
Descripción
Sumario: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.