The role of 3D microenvironmental organization in MCF-7 epithelial-mesenchymal transition after 7 culture days

Exp Cell Res. 2013 Jun 10;319(10):1515-22. doi: 10.1016/j.yexcr.2013.03.035. Epub 2013 Apr 11.

Abstract

We present a multi-technique study on in vitro epithelial-mesenchymal transition (EMT) in human MCF-7 cells cultured on electrospun scaffolds of poly(l-lactic acid) (PLA), with random and aligned fiber orientations. Our aim is to investigate the morphological and genetic characteristics induced by extracellular matrix in tumor cells cultured in different 3D environments, and at different time points. Cell vitality was assessed with AlamarBlue at days 1, 3, 5 and 7. Scanning electron microscopy was performed at culture days 3 and 7. Immunohistochemistry (for E-cadherin, β-catenin, cytokeratins, nucleophosmin, tubulin, Ki-67 and vimentin), immunofluorescence (for F-actin) western blot (for E-cadherin, β-catenin and vimentin) and transmission electron microscopy were carried out at day 7. An EMT gene array followed by PCR analysis confirmed the regulation of selected genes. At day 7, scanning electron microscopy on aligned-PLA revealed spindle-shaped cells gathered in buds and ribbon-like structures, with a higher nucleolar/nuclear ratio and a loss in E-cadherin and β-catenin at immunohistochemistry and western blot. An up-regulation of SMAD2, TGF-β2, TFPI2 and SOX10 was found in aligned-PLA compared to random-PLA cultured cells. The topography of the extracellular matrix has a role in tumor EMT, and a more aggressive phenotype characterizes MCF-7 cells cultured on aligned-PLA scaffold.

MeSH terms

  • Actins / genetics
  • Actins / metabolism
  • Antigens, CD
  • Blotting, Western
  • Cadherins / genetics
  • Cadherins / metabolism
  • Cell Adhesion
  • Cell Shape*
  • Epithelial-Mesenchymal Transition*
  • Extracellular Matrix / metabolism*
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Glycoproteins / genetics
  • Glycoproteins / metabolism
  • Humans
  • Immunohistochemistry
  • Ki-67 Antigen / genetics
  • Ki-67 Antigen / metabolism
  • Lactic Acid / metabolism
  • MCF-7 Cells
  • Microscopy, Electron, Scanning
  • Microscopy, Electron, Transmission
  • Oligonucleotide Array Sequence Analysis
  • Oxazines
  • Phenotype
  • Smad2 Protein / genetics
  • Smad2 Protein / metabolism
  • Time Factors
  • Tissue Scaffolds
  • Transforming Growth Factor beta2 / genetics
  • Transforming Growth Factor beta2 / metabolism
  • Tumor Microenvironment*
  • Vimentin / genetics
  • Vimentin / metabolism
  • Xanthenes
  • beta Catenin / genetics
  • beta Catenin / metabolism

Substances

  • Actins
  • Antigens, CD
  • CDH1 protein, human
  • CTNNB1 protein, human
  • Cadherins
  • Glycoproteins
  • Ki-67 Antigen
  • Oxazines
  • SMAD2 protein, human
  • Smad2 Protein
  • Transforming Growth Factor beta2
  • Vimentin
  • Xanthenes
  • beta Catenin
  • tissue-factor-pathway inhibitor 2
  • resazurin
  • Lactic Acid