Effects of the MCF-7 Exhausted Medium on hADSC Behaviour

Int J Mol Sci. 2024 Jun 27;25(13):7026. doi: 10.3390/ijms25137026.

Abstract

Stem cells possess the ability to differentiate into different lineages and the ability to self-renew, thus representing an excellent tool for regenerative medicine. They can be isolated from different tissues, including the adipose tissue. Adipose tissue and human adipose-derived stem cells (hADSCs) are privileged candidates for regenerative medicine procedures or other plastic reconstructive surgeries. The cellular environment is able to influence the fate of stem cells residing in the tissue. In a previous study, we exposed hADSCs to an exhausted medium of a breast cancer cell line (MCF-7) recovered at different days (4, 7, and 10 days). In the same paper, we inferred that the medium was able to influence the behaviour of stem cells. Considering these results, in the present study, we evaluated the expression of the major genes related to adipogenic and osteogenic differentiation. To confirm the gene expression data, oil red and alizarin red colorimetric assays were performed. Lastly, we evaluated the expression of miRNAs influencing the differentiation process and the proliferation rate, maintaining a proliferative state. The data obtained confirmed that cells exposed to the medium maintained a stem and proliferative state that could lead to a risky proliferative phenotype.

Keywords: ADSC; conditioned media; epigenetic mechanism; miRNA; stem cell differentiation; stem cells.

MeSH terms

  • Adipogenesis / genetics
  • Adipose Tissue* / cytology
  • Adipose Tissue* / metabolism
  • Cell Differentiation* / drug effects
  • Cell Proliferation* / drug effects
  • Culture Media / chemistry
  • Culture Media / pharmacology
  • Female
  • Humans
  • MCF-7 Cells
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Osteogenesis* / drug effects
  • Osteogenesis* / genetics
  • Stem Cells / cytology
  • Stem Cells / drug effects
  • Stem Cells / metabolism

Substances

  • MicroRNAs
  • Culture Media

Grants and funding

This research received no external funding.