Review
Copyright ©2014 Baishideng Publishing Group Inc.
World J Stem Cells. Nov 26, 2014; 6(5): 511-525
Published online Nov 26, 2014. doi: 10.4252/wjsc.v6.i5.511
Figure 1
Figure 1 Data represents acetylation status of histone 3 in Head and Neck Squamous Cell Carcinoma by Giudice et al[151]. A: Tumor cells present hypoacetylation of histone 3 (ac.H3) in a panel of Head and Neck Squamous Cell Carcinoma (HNSCC) compared to control cells (NOK-SI); B: Endothelial cell-secreted factors are capable of inducing ac.H3 while fibroblast cell-secreted factors cannot. Also, endothelial cell-secreted factors induce increased expression of BMI-1 and vimentin compared to the fibroblast counterpart; C: Representative examples of human samples of normal oral mucosa and HNSCC. Note acetylated tumor cells (Ac. H3-FITC) with high levels of the epithelial-mesenchymal transition marker vimentin (TRICT) are localized at the invasion front of HNSCC (arrow). Normal mucosa display acetylated cells distributed throughout the epidermis but do not express vimentin. ac. H3: Acetyl histone 3; GAPDH: Glyceraldehyde-3-phosphate dehydrogenase; CM: Conditioned Media; BMI-1: B lymphoma Mo-MLV insertion region 1 homolog; NOK-SI: Normal oral epithelial keratinocytes.