AI Summary & Key Takeaways
AI InsightWhen using BM-MSCs in cancer studies, it should be taken into consideration that the cancerization process may affect the production of connexin 43 and the ability of the cells to adhere.
📌 3 Key Takeaways
Abstract
The aim of this study was to examine how zinc and BMP2 affected the amount of connexin 43 produced by BM-MSCs stimulated with DMBA. BM-MSCs were identified after being generated in a cell culture. BM-MSCs were exposed to combinations of 24 nM DMBA, 1 µM zinc, and 10 ng/mL BMP2. Using immunofluorescence methods, the effects of zinc, BMP2, and DMBA on the formation of connexin 43 in BM-MSCs were assessed. In the present study, BM-MSCs were produced and identified. As a result of immunofluorescence, connexin 43 expression was somewhat downregulated in the BMP2, zinc, and DMBA single applications; this downregulation was more pronounced in the double and triple applications. Zinc concentrations in the medium where BM-MSCs are produced may affect the results of preclinical and clinical studies based on transplantation through the adhesion ability of the cells, depending on the toxic effect. When using BM-MSCs in cancer studies, it should be taken into consideration that the cancerization process may affect the production of connexin 43 and the ability of the cells to adhere.