Université Catholique de Louvain (UCLouvain), Louvain Drug Research Institute, Advanced Drug Delivery and Biomaterials, 1200 Brussels, Belgium.
Université Catholique de Louvain (UCLouvain), Institut de Recherche Expérimentale et Clinique, Pole of Pharmacology and Therapeutics, 1200 Brussels, Belgium.
Int J Pharm. 2020 Jun 30;584:119337. doi: 10.1016/j.ijpharm.2020.119337. Epub 2020 May 1.
Crosstalk between cancer-associated fibroblasts (CAFs) and colorectal cancer cells promotes tumor growth and contributes to chemoresistance. In this study, we assessed the sensitivity of a primary CAF cell line, CT5.3hTERT, to standard-of-care and alternative cytotoxic treatments. Paclitaxel (PTX) and acriflavine (ACF) were identified as the most promising molecules to inhibit CAF development. To allow the translational use of both drugs, we developed lipid nanocapsule (LNC) formulations for PTX and ACF. Finally, we mixed CAFs and tumor cell lines in a cocultured spheroid, and the effect of both drugs was investigated by histological analyses. We demonstrated CAF inhibition by LNC-ACF and whole tumor inhibition by LNC-PTX. Altogether, we proposed a new strategy to reduce CAF populations in the colorectal microenvironment that should be tested in vivo.
肿瘤相关成纤维细胞 (CAFs) 与结直肠癌细胞之间的串扰促进肿瘤生长并导致化疗耐药。在本研究中,我们评估了原代 CAF 细胞系 CT5.3hTERT 对标准治疗和替代细胞毒性治疗的敏感性。紫杉醇 (PTX) 和吖啶黄素 (ACF) 被确定为最有希望抑制 CAF 发展的分子。为了使这两种药物能够进行转化应用,我们开发了用于 PTX 和 ACF 的脂质纳米胶囊 (LNC) 制剂。最后,我们将 CAFs 和肿瘤细胞系混合在共培养的球体中,并通过组织学分析研究了这两种药物的作用。我们证明了 LNC-ACF 对 CAF 的抑制作用和 LNC-PTX 对整个肿瘤的抑制作用。总之,我们提出了一种新的策略来减少结直肠微环境中的 CAF 群体,该策略应在体内进行测试。