Page 112 - D. Cancer biology
P. 112

[D. Cancer biology-71]



              Effect of HDAC inhibitor Apicidin on epithelial-mesenchymal


               transition and cell migration in human oral squamous cell


                                                carcinoma cells








                  A-Reum Choi¹, Seong-Min Kwon², Andre Kim¹, Jung-Hoon Yoon², Mee-Young Ahn¹˙*

          ¹Department of Pharmaceutical Engineering, College of Medical and Life Sciences, Silla University, Busan 46958,

             Republic of Korea, ²Department of Oral & Maxillofacial Pathology, College of Dentistry, Wonkwang Bone
              Regeneration Research Institute, Daejeon Dental Hospital, Wonkwa, Daejeon 35233, Republic of Korea





        This study investigated the effect of HDAC inhibitor apicidin on epithelial-mesenchymal transition (EMT) and cell
        migration of human oral squamous cell carcinoma (OSCC) cells. EMT markers and transcription factors were detected
        by western blot. Wounded healing assay and transwell migration assay were performed to detect cell migration.

        The expression of migration-related proteins was examined by western blot and zymography. Apicidin increased E-
        cadherin expression and  decreased Vimentin  expression in  human  OSCC  cells.  The  levels  of  Zeb1  and  Slug

        expression were decreased, but the level of Snail expression was increased by apicidin. Apicidin markedly blocked
        wounded  healing  and  cell  migration  of  human  OSCC  cells.  Down-regulation  of  MMP-2  and  MMP-9  and  up-

        regulation of TIMP2 was detected on apicidin treated OSCC cells. These results suggest that Apicidin can reverse
        EMT, thereby inhibiting the migration of OSCC cells. HDAC inhibitor Apicidin may potentially be used as an anti-

        cancer  agent  for  inhibition  of  cancer cell  EMT  and  migration.  Further  study  will  be  needed.  This research  was
        supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by

        the Ministry of Education, Science and Technology (NRF-2019R1F1A1041002).
   107   108   109   110   111   112   113   114   115   116   117