Silicate fiber-based 3D cell culture system for anticancer drug screening

Anticancer Res. 2013 Dec;33(12):5301-9.

Abstract

Background: Three-dimensional (3D) in vitro cultures can recapitulate the physiological in vivo microenvironment. 3D Modeling techniques have been investigated and applied in anticancer drug screening.

Materials and methods: A silicate fiber scaffold was used for 3D cell cultures, and used to model the efficacy of anticancer drugs, such as mytomicin C and doxorubicin.

Results: A unique 3D structure was observed in 13 human tumor cell lines on scaffold, and these cells exhibited higher drug resistance than cells in two-dimensional (2D) cultures. Furthermore, the production of lactate and expression of the nuclear factor-kappa B (NF-κB)-regulated genes B cell lymphoma-2 (BCL2), cyclooxygenase-2 (COX2), and vascular endothelial growth factor (VEGF) were higher in 3D cultures than in 2D cultures.

Conclusion: These findings suggest that a 3D model using a silicate fiber scaffold can mimic features of cancer, and is also a suitable model for the evaluation of anticancer drugs in vitro.

Keywords: Three-dimensional (3D) culture; anticancer drug screening; drug resistance; silicate fiber scaffold.

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Base Sequence
  • Cell Culture Techniques / methods*
  • Cell Line, Tumor
  • Cyclooxygenase 2 / metabolism
  • DNA Primers
  • Doxorubicin / pharmacology
  • Drug Screening Assays, Antitumor / methods*
  • Gene Expression Regulation / physiology
  • Glycolysis
  • Humans
  • Mitomycin / pharmacology
  • NF-kappa B / physiology
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Real-Time Polymerase Chain Reaction
  • Silicates*
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Antineoplastic Agents
  • DNA Primers
  • NF-kappa B
  • Proto-Oncogene Proteins c-bcl-2
  • Silicates
  • Vascular Endothelial Growth Factor A
  • Mitomycin
  • Doxorubicin
  • Cyclooxygenase 2