AI Article Synopsis

  • The study investigates the effects of lipotransfer on breast tissue post-irradiation in breast cancer patients, highlighting its widespread use despite unresolved safety concerns.
  • The research involved co-culturing mammary epithelial cells with fibroblasts and examining the impact of conditioned medium from adipose-derived stem cells, revealing that this treatment may enhance certain harmful cellular behaviors.
  • The findings suggest that while lipotransfer might offer benefits, it carries potential risks, emphasizing the need for cautious evaluation in clinical practice.

Article Abstract

The application of lipotransfer after breast-conserving therapy (BCT) and irradiation in breast cancer patients is an already widespread procedure for reconstructing volume deficits of the diseased breast. Nevertheless, the safety of lipotransfer has still not been clarified yet due to contradictory data. The goal of this in vitro study was to further elucidate the potential effects of lipotransfer on the irradiated remaining breast tissue. The mammary epithelial cell line MCF-10A was co-cultured with the fibroblast cell line MRC-5 and irradiated with 2 and 5 Gy. Afterwards, cells were treated with conditioned medium (CM) from adipose-derived stem cells (ADSC), and the effects on the cellular functions of MCF-10A cells and on gene expression at the mRNA level in MCF-10A and MRC-5 cells were analyzed. Treatment with ADSC CM stimulated transmigration and invasion and decreased the surviving fraction of MCF-10A cells. Further, the expression of cytokines, extracellular, and mesenchymal markers was enhanced in mammary epithelial cells. Only an effect of ADSC CM on irradiated fibroblasts could be observed. The present data suggest epithelial-mesenchymal transition-like changes in the epithelial mammary breast cell line. Thus, the benefits of lipotransfer after BCT should be critically weighed against its possible risks for the affected patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9409821PMC
http://dx.doi.org/10.3390/jpm12081284DOI Listing

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