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Fucoxanthin Holds Potential to Become a Drug Adjuvant in Breast Cancer Treatment: Evidence from 2D and 3D Cell Cultures

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2021 Jul 24
PMID 34299562
Citations 11
Authors
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Abstract

Fucoxanthin (Fx) is a carotenoid derived from marine organisms that exhibits anticancer activities. However, its role as a potential drug adjuvant in breast cancer (BC) treatment is still poorly explored. Firstly, this study investigated the cytotoxic effects of Fx alone and combined with doxorubicin (Dox) and cisplatin (Cis) on a panel of 2D-cultured BC cell lines (MCF7, SKBR3 and MDA-MB-231) and one non-tumoral cell line (MCF12A). Fucoxanthin induced cytotoxicity against all the cell lines and potentiated Dox cytotoxic effects towards the SKBR3 and MDA-MB-231 cells. The combination triggering the highest cytotoxicity (Fx 10 µM + Dox 1 µM in MDA-MB-231) additionally showed significant induction of cell death and genotoxic effects, relative to control. In sequence, the same combination was tested on 3D cultures using a multi-endpoint approach involving bioactivity assays and microscopy techniques. Similar to 2D cultures, the combination of Fx and Dox showed higher cytotoxic effects on 3D cultures compared to the isolated compounds. Furthermore, this combination increased the number of apoptotic cells, decreased cell proliferation, and caused structural and ultrastructural damages on the 3D models. Overall, our findings suggest Fx has potential to become an adjuvant for Dox chemotherapy regimens in BC treatment.

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References
1.
Imamura Y, Mukohara T, Shimono Y, Funakoshi Y, Chayahara N, Toyoda M . Comparison of 2D- and 3D-culture models as drug-testing platforms in breast cancer. Oncol Rep. 2015; 33(4):1837-43. DOI: 10.3892/or.2015.3767. View

2.
Leon-Galicia I, Diaz-Chavez J, Albino-Sanchez M, Garcia-Villa E, Bermudez-Cruz R, Garcia-Mena J . Resveratrol decreases Rad51 expression and sensitizes cisplatin‑resistant MCF‑7 breast cancer cells. Oncol Rep. 2018; 39(6):3025-3033. DOI: 10.3892/or.2018.6336. View

3.
Dai J, Jian J, Bosland M, Frenkel K, Bernhardt G, Huang X . Roles of hormone replacement therapy and iron in proliferation of breast epithelial cells with different estrogen and progesterone receptor status. Breast. 2007; 17(2):172-9. PMC: 2957482. DOI: 10.1016/j.breast.2007.08.009. View

4.
Verjans E, Doijen J, Luyten W, Landuyt B, Schoofs L . Three-dimensional cell culture models for anticancer drug screening: Worth the effort?. J Cell Physiol. 2017; 233(4):2993-3003. DOI: 10.1002/jcp.26052. View

5.
Liston D, Davis M . Clinically Relevant Concentrations of Anticancer Drugs: A Guide for Nonclinical Studies. Clin Cancer Res. 2017; 23(14):3489-3498. PMC: 5511563. DOI: 10.1158/1078-0432.CCR-16-3083. View