“…It could be proposed that the cells entered into the senescence phase, the upregulation of some metastatic and cancerrelated genes led us to hypothesis whether cell characteristics might change with increased passaging. In addition, downregulation of other genes such as secreted frizzled-related protein 1 (SFRP1), survivin (BIRC5), and BUB1, which play a role in regulation of the Wnt signaling pathway [66,67], inhibition of apoptosis [68][69][70], and regulation of spindle check point proteins [71][72][73], respectively, have supported this hypothesis. Upregulation of some developmental, metastatic, and cancer-related genes in addition to downregulation of cell cycle-related genes, which was observed in our microarray results, indicated the distinct properties of the cells in higher passages compared to those in low passages.…”