Profilin 2 promotes migration, invasion, and stemness of HT29 human colorectal cancer stem cells

Biosci Biotechnol Biochem. 2015;79(9):1438-46. doi: 10.1080/09168451.2015.1043118. Epub 2015 May 12.

Abstract

We investigated the role of profilin 2 in the stemness, migration, and invasion of HT29 cancer stem cells (CSCs). Increased and decreased levels of profilin 2 significantly enhanced and suppressed the self-renewal, migration, and invasion ability of HT29 CSCs, respectively. Moreover, profilin 2 directly regulated the expression of stemness markers (CD133, SOX2, and β-catenin) and epithelial mesenchymal transition (EMT) markers (E-cadherin and snail). CD133 and β-catenin were up-regulated by overexpression of profilin 2 and down-regulated by depletion of profilin 2. SOX2 was decreased by profilin 2 depletion. E-cadherin was not influenced by profilin 2- overexpression but increased by profilin 2- knockdown. The expression of snail was suppressed by profilin 2- knockdown. We speculated that stemness and the EMT are closely linked through profilin 2-related pathways. Therefore, this study indicates that profilin 2 affects the metastatic potential and stemness of colorectal CSCs by regulating EMT- and stemness-related proteins.

Keywords: Cancer stem cells (CSCs); Invasion; Migration; Profilin 2; Stemness.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cell Movement / genetics
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / pathology
  • Epithelial-Mesenchymal Transition / genetics
  • Gene Expression Regulation, Neoplastic
  • Gene Knockdown Techniques
  • HT29 Cells
  • Humans
  • Neoplasm Invasiveness / genetics
  • Neoplasm Proteins / biosynthesis*
  • Neoplastic Stem Cells*
  • Profilins / biosynthesis
  • Profilins / genetics*
  • Wnt Signaling Pathway / genetics
  • beta Catenin / biosynthesis

Substances

  • Neoplasm Proteins
  • PFN2 protein, human
  • Profilins
  • beta Catenin