Aluated the protein expression of Cyclin D1 in SACC cells after JQ1 treatment. We found that the protein levels of Cyclin D1 were significantly decreased in ACC-LM cells treated with JQ1 at concentration of 0.5 and 1 (Fig. 5a). Similarly, the protein levels of CyclinEpithelial esenchymal transition plays pivotal roles in tumor development and invasion, and is a key initiating event in the metastatic cascade. To investigate the molecular mechanism of the inhibition of JQ1 on migration and invasion of SACC cells, the levels of several EMT purchase Tariquidar related proteins were examined. The results showed that the protein level of Twist was significantly repressed in ACC-LM and ACC-83 cells (Fig. 7) treated with JQ1 at various concentrations after 24 and 48 h when compared with the control group. Moreover, the protein levels of Vimentin were significantly down-regulated by JQ1 at concentrations of 0.5 and 1 in ACC-LM and ACC-83 cells (Fig. 7). The protein level of epithelial gene, E-cadherin, was up-regulated in ACC-LM and ACC-83 cells treated with JQ1 (Fig. 7). These results suggest that the inhibition effect of JQ1 on SACC cell migration and invasion may be due to EMT inhibition.Discussion BRD4 inhibition suppresses growth and metastasis of several malignant tumors and BRD4 has been validated as a therapeutic target for tumor treatment [5, 26, 28, 29].Wang et al. Biol Res (2017) 50:Page 5 ofFig. 3 JQ1 induces apoptosis and inhibits cell cycle in SACC cells. a The protein levels of cleaved cl-C3 in ACC-LM and ACC-83 cells treated with JQ1 at various concentrations for 48 h; b apoptosis of ACC-LM cells and ACC-83 cells treated with JQ1 at concentration of 1 for 48 h; c the fractions of ACC-LM cells and ACC-83 cells in each phase of the cell cycle are shown after JQ1 treatment at the concentration of 1 for 48 h. *P < 0.05 vs. the control group (the DMSO group). cl-C3 cleaved caspase-Wang et al. Biol Res (2017) 50:Page 6 ofFig. 4 JQ1 inhibits BRD4 expression in SACC cells. a The mRNA levels of BRD4 in PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/27689333 ACC-LM and ACC-83 cells treated with JQ1 for 24 and 48 h. b The protein levels of BRD4 in ACC-LM and ACC-83 cells treated with JQ1 for 24 and 48 h; c immunofluorescence staining of BRD4 in ACC-LM and ACC-83 cells treated with JQ1 at the concentration of 1 for 24 h (?00). *P < 0.05 vs. the control group (the DMSO group)Wang et al. Biol Res (2017) 50:Page 7 ofFig. 5 JQ1 down-regulates Cyclin D1, c-myc and BCL-2 expressions in SACC cells. a The protein levels of Cyclin D1 and c-myc in ACC-LM cells and ACC-83 cells treated with JQ1 at various concentrations for 48 h; b the protein levels of BCL-2 in ACC-LM cells and ACC-83 cells treated with JQ1 at various concentrations for 48 h. *P < 0.05 vs. the control group (the DMSO group)Wang et al. Biol Res (2017) 50:Page 8 ofFig. 6 JQ1 inhibits the migration and invasion of SACC cells. a The migration of ACC-LM cells and ACC-83 cells treated by JQ1 at various concentrations for 20 h (?00); b the invasion of ACC-LM cells and ACC-83 cells treated by JQ1 at various concentrations for 20 h (?00). *P < 0.05 vs. the control group (the DMSO group)Wang et al. Biol Res (2017) 50:Page 9 ofFig. 7 JQ1 represses several key EMT characteristics in SACC cells. The protein levels of E-cadherin, Vimentin and Twist in ACC-LM (a) and ACC-83 (b) cells treated with JQ1 for 24 and 48 h. *P < 0.05 vs. the control group (the DMSO group)Wang et al. Biol Res (2017) 50:Page 10 ofHowever, the effect of BRD4 inhibition on SACC has not be.