BackgroundStem cells constitute a group of great capacity for self-renewal, long-term viability, and multi-lineage potential. Several studies have provided evidence that adipose tissue represents an alternative source of stem cells, with the main benefit of adipose-derived stem cells being that they can be easily harvested from patients by a simple minimally invasive method and can be easily cultured. The aim of this study was to establish a culture protocol for obtaining and characterizing adipose-derived stem cells (ADSCs) from C57BL/6 J mice.ResultsThe results showed that the yield, viability, and cell morphology obtained differ according to the age of isolated anatomic regions of the adipose tissue from ovarian and epididymis. The results of determination of cyclin D1 showed uniformity in the expression between different populations of ADSCs. A significant increase in the expression of caspase-3 active, was also observed in large cell populations from mice after 120 days. ADSCs were positive for mesenchymal markers CD90 and CD105, Nanog, SSEA-1, CD106, and VEGFR-1, and negative for hematopoietic markers CD34 and CD45. A large number of cells in S + G2/M phases was also observed for both sexes, demonstrating high proliferative capacity of ADSCs.ConclusionsWe observed that the adipose tissue of C57BL/6 J mice, isolated from the studied anatomic regions, is a promising source for obtaining pluripotent mesenchymal stem cells with high viability and proliferative response.

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Resistance to the therapies currently offered for melanoma and hepatocellular carcinoma requires new research that seeks more effective therapeutic agents with less toxicity. The present study aimed to evaluate the antiproliferative, antitumor effects and the modulation of the mitochondrial electrical potential of the Acetate and Chloroform fractions and the sub-fractions Methanol, Ethanol, Dichloromethane and Ether, isolated from E. umbellata latex sap in murine melanoma cells (B16 -F10), hepatocellular carcinoma tumor cells (Hepa1c1c7) and normal fibroblast cells (FN1). The Acetate and Chloroform fractions showed significantly cytotoxic potential for tumor cells B16-F10 and Hepa1c1c7, in addition to the fractions being sensitive to the ether and methanol compounds. Such compounds promoted the reduction of cell confluence, the modulation of mitochondrial electrical potential, the depolarization of the mitochondrial membrane, and the release of pro-apoptotic mechanisms that resulted in the death of both tumor lines.