Abstract

Preussin, a hydroxyl pyrrolidine derivative isolated from the marine sponge-associated fungus Aspergillus candidus KUFA 0062, displayed anticancer effects in some cancer cell lines, including MCF7. Preussin was investigated for its cytotoxic and antiproliferative effects in breast cancer cell lines (MCF7, SKBR3, and MDA-MB-231), representatives of major breast cancers subtypes, and in a non-tumor cell line (MCF12A). Preussin was first tested in 2D (monolayer), and then in 3D (multicellular aggregates), cultures, using a multi-endpoint approach for cytotoxicity (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), resazurin and lactate dehydrogenase (LDH)) and proliferative (5-bromo-2′-deoxyuridine (BrdU)) assays, as well as the analysis of cell morphology by optical/electron microscopy and immunocytochemistry for caspase-3 and ki67. Preussin affected cell viability and proliferation in 2D and 3D cultures in all cell lines tested. The results in the 3D culture showed the same tendency as in the 2D culture, however, cells in the 3D culture were less responsive. The effects were observed at different concentrations of preussin, depending on the cell line and assay method. Morphological study of preussin-exposed cells revealed cell death, which was confirmed by caspase-3 immunostaining. In view of the data, we recommend a multi-endpoint approach, including histological evaluation, in future assays with the tested 3D models. Our data showed cytotoxic and antiproliferative activities of preussin in breast cancer cell lines in 2D and 3D cultures, warranting further studies for its anticancer potential.

Highlights

  • Since cancer incidence keeps rising each year [1,2], the scientific community and pharmaceutical industry have focused their attention on the discovery of new drugs or drug adjuvants to improve the fight against this disease [3]

  • Cells were exposed for 72 h either to preussin (1) at different concentrations

  • Cells exposed to preussin (1) at 50 and 100 μM showed significant decrease in cell viability in the three cancer cell lines (MCF7, MDA-MB-231, and SKBR3) and in the non-tumor cell line (MCF12A)

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Summary

Introduction

Since cancer incidence keeps rising each year [1,2], the scientific community and pharmaceutical industry have focused their attention on the discovery of new drugs or drug adjuvants to improve the fight against this disease [3]. One hotspot of interest for drug discovery is anticancer drugs, whose rising costs have been applied to drug research and development [3,4]. Mar. Drugs 2019, 17, 448; doi:10.3390/md17080448 www.mdpi.com/journal/marinedrugs. Oceans cover 70% of the Earth’s surface, and represent a variety of environmental niches, due to different salinities, pressures, light and oxygen levels, nutrient availability, and temperatures, which result in a great diversity of marine fauna and flora.

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