Inhibition of colorectal cancer-associated fibroblasts by lipid nanocapsules loaded with acriflavine or paclitaxel

Int J Pharm. 2020 Jun 30:584:119337. doi: 10.1016/j.ijpharm.2020.119337. Epub 2020 May 1.

Abstract

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.

Keywords: Acriflavine; Cancer-associated fibroblast; Lipid nanocapsule; Paclitaxel; Tumor spheroid.

MeSH terms

  • Acriflavine / administration & dosage
  • Acriflavine / pharmacology*
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / pharmacology*
  • Cancer-Associated Fibroblasts / drug effects*
  • Cell Line, Tumor
  • Cell Survival
  • Chemistry, Pharmaceutical / methods
  • Colorectal Neoplasms / drug therapy
  • Colorectal Neoplasms / pathology
  • Drug Carriers / administration & dosage
  • Drug Carriers / pharmacology
  • HCT116 Cells
  • Humans
  • Lipids / chemistry
  • Nanocapsules / chemistry*
  • Paclitaxel / administration & dosage
  • Paclitaxel / pharmacology*
  • Tumor Microenvironment / drug effects

Substances

  • Antineoplastic Agents
  • Drug Carriers
  • Lipids
  • Nanocapsules
  • Acriflavine
  • Paclitaxel