Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto (U.Porto), Rua de Jorge Viterbo Ferreira 228, 4050-313 Porto, Portugal.
Interdisciplinary Center for Marine and Environmental Research (CIIMAR), University of Porto (U.Porto), Avenida General Norton de Matos, 4450-208 Matosinhos, Portugal.
Molecules. 2021 Jul 15;26(14):4288. doi: 10.3390/molecules26144288.
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.
岩藻黄质(Fx)是一种从海洋生物中提取的类胡萝卜素,具有抗癌活性。然而,其作为乳腺癌(BC)治疗中潜在药物佐剂的作用仍未得到充分探索。首先,本研究在一系列二维培养的 BC 细胞系(MCF7、SKBR3 和 MDA-MB-231)和一个非肿瘤细胞系(MCF12A)中,单独及联合多柔比星(Dox)和顺铂(Cis)研究了 Fx 的细胞毒性作用。岩藻黄质对所有细胞系均诱导细胞毒性,并增强 Dox 对 SKBR3 和 MDA-MB-231 细胞的细胞毒性作用。组合触发的最高细胞毒性(MDA-MB-231 中 Fx 10 μM + Dox 1 μM),与对照组相比,还显示出显著的细胞死亡和遗传毒性作用诱导。随后,使用涉及生物活性测定和显微镜技术的多终点方法,在 3D 培养物上测试了相同的组合。与 2D 培养物相似,Fx 和 Dox 的组合在 3D 培养物上的细胞毒性作用高于单独化合物。此外,该组合增加了凋亡细胞数量,降低了细胞增殖,并在 3D 模型上引起了结构和超微结构损伤。总的来说,我们的研究结果表明,Fx 有可能成为 BC 治疗中 Dox 化疗方案的佐剂。