Adipose-Derived Stem Cell Features and MCF-7

Cells. 2021 Jul 11;10(7):1754. doi: 10.3390/cells10071754.

Abstract

Human adipose tissue-derived stem cells (hADSCs) are highly suitable for regeneration therapies being easily collected and propagated in vitro. The effects of different external factors and culturing conditions are able to affect hADSC proliferation, senescence, differentiation, and migration, even at the molecular level. In the present paper, we exposed hADSCs to an exhausted medium from the breast cancer cell line (MCF-7) to evaluate whether the soluble factors released by these cells may be able to induce changes in stem cell behavior. In particular, we investigated the expression of stemness-related genes (OCT4; Sox 2; Nanog), the cell-cycle regulators p21 (WAF1/CIP1) p53, epigenetic markers (DNMT1 and Sirt1), and autophagy-related proteins. From our results, we can infer that the exhausted medium from MCF-7 is able to influence the hADSCs behavior increasing the expression of stemness-related genes, cell proliferation, and autophagy. Polyamines detectable in MCF-7 exhausted medium could be related to the higher proliferation capability observed in hADSCs, suggesting direct crosstalk between these molecules and the observed changes in stem cell potency.

Keywords: adipose-derived stem cells; autophagy; cell proliferation; cellular mechanisms; epigenetics; stemness genes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / cytology*
  • Autophagosomes / metabolism
  • Autophagy / genetics
  • Bromodeoxyuridine / metabolism
  • Cell Proliferation
  • Cell Shape
  • Cell Survival
  • Culture Media
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism
  • Epigenesis, Genetic
  • Humans
  • MCF-7 Cells
  • Middle Aged
  • Polyamines / metabolism
  • Stem Cells / cytology*
  • Stem Cells / metabolism
  • Tumor Suppressor Protein p53 / metabolism
  • bcl-2-Associated X Protein / metabolism

Substances

  • Culture Media
  • Cyclin-Dependent Kinase Inhibitor p21
  • Polyamines
  • Tumor Suppressor Protein p53
  • bcl-2-Associated X Protein
  • Bromodeoxyuridine