a Team of Histomorphology, Physiopathology and Applied Toxicology, CIIMAR - Interdisciplinary Center for Marine and Environmental Research, University of Porto , Matosinhos , Portugal.
b Laboratory of Histology and Embryology, Department of Microscopy, ICBAS - Institute of Biomedical Sciences Abel Salazar, University of Porto , Porto , Portugal.
J Toxicol Environ Health A. 2019;82(9):537-549. doi: 10.1080/15287394.2019.1634378. Epub 2019 Jun 30.
Colorectal cancer (CRC) is one of the most frequently occurring carcinomas which require effective therapies. Fucosterol is a sterol present in marine brown seaweeds with several biological activities. However, the influence of fucosterol in CRC remains to be determined. Thus, the aim of this study was to examine the anticancer activity of fucosterol alone and in combination with 5-fluorouracil (5-Fu) on two human CRC cell lines (HCT116 and HT29) and compared with cytotoxicity in one normal colon fibroblast cell line (CCD-18co) in monolayer (2D). The effect of fucosterol alone or in combination with 5-Fu was further assessed using HT29 multicellular spheroids (3D). Data demonstrated that fucosterol alone or combined with 5-Fu decreased cell viability in HT29 cells in 2D cultures without inducing cytotoxic in normal colon cells. The combination, fucosterol, and 5-Fu, also inhibited cell proliferation, clonogenic potential and cell migration without producing cell death in 2D. In multicellular spheroids, the combination fucosterol plus 5-Fu at the same concentrations used in 2D was not effective demonstrating that under the tested conditions the 3D model was more resistant than the 2D model. Taken together, these findings suggest that fucosterol might be a promising alternative to enhance the cytotoxic and anti-invasive actions of 5-Fu in colon cancer cells without consequent major adverse effects in normal cells. Our results also reinforce the need to include more complex 3D culture models in the initial stages of drug screening.
结直肠癌(CRC)是最常见的癌种之一,需要有效的治疗方法。岩藻甾醇是一种存在于海洋褐藻中的甾醇,具有多种生物学活性。然而,岩藻甾醇在 CRC 中的影响仍有待确定。因此,本研究旨在研究岩藻甾醇单独及与 5-氟尿嘧啶(5-Fu)联合对两种人 CRC 细胞系(HCT116 和 HT29)的抗癌活性,并与单层(2D)中一种正常结肠成纤维细胞系(CCD-18co)的细胞毒性进行比较。还使用 HT29 多细胞球体(3D)进一步评估了岩藻甾醇单独或与 5-Fu 联合的作用。数据表明,岩藻甾醇单独或与 5-Fu 联合在 2D 培养物中降低 HT29 细胞的活力,而不会诱导正常结肠细胞的细胞毒性。联合使用岩藻甾醇和 5-Fu 也抑制细胞增殖、克隆形成潜力和细胞迁移,而不会在 2D 中产生细胞死亡。在多细胞球体中,在 2D 中使用的相同浓度的岩藻甾醇加 5-Fu 的组合无效,表明在测试条件下,3D 模型比 2D 模型更具抗性。总之,这些发现表明,岩藻甾醇可能是增强 5-Fu 在结肠癌细胞中细胞毒性和抗侵袭作用的有前途的替代物,而不会对正常细胞产生严重的不良反应。我们的结果还强调了在药物筛选的初始阶段需要包括更复杂的 3D 培养模型。