<p>(A) PC3 and LNCaP cells were treated with TSA or SAHA at different doses for 48 h. Western blot analysis showing the expression of epithelial and meshenchymal markers as well as acetylating status. (B) TSA treatment for 48 h increased the expression of Sox2 and Nanog in a dose dependent manner in PC3 PDGF-D cells. Up-regulation of vimentin was seen even after 50 nM TSA of treatment. (C) Cell detachment assay was performed after 400 nM TSA or 5 µM SAHA treatment for 20 h. TSA and SAHA significantly promoted PC3 cell detachment from culture surfaces (**, p<0.01). (D) Showing increased trends of cell migration of PC3 cells treated with TSA and SAHA.</p
<p>(A) FaDu, Cal-27, and Hep-2 cells were treated with indicated concentrations of DHA for 24 or 48h...
<p>(A) <i>BLM</i> and (B) <i>XPA</i> human lymphocytes were treated with 0 to 1.5 µM TSA or 0 to 100...
<p><b>A</b>. Apoptosis of PBMCs, PBLs, and monocytes from healthy controls after treatment with TSA ...
<p>(A and B) PC3 cells treated with TSA and SAHA for 24 h at indicated doses. The photomicrographs o...
<p>(A) Total RNA was isolated from LNCaP cells treated with 200 nM and 400 nM TSA for 8, 16 and 24 h...
<p>(A) CHIP assay was conducted to determine the binding of HDACs and acetylation status of histone ...
<p>Total RNA was isolated from PC3 cells treated with 200 nM and 400 nM TSA (A) or 2.5 µM and 5 µM S...
<p>SGC-996 cells were treated with or without different concentrations of TSA or SAHA for 24 h. The ...
Clinical experience of histone deacetylase inhibitors (HDACIs) in patients with solid tumors has bee...
<p>A–B: TSA treatment caused increased expression of TGF-α. Myofibroblasts were treated with theo (t...
<p>(A) Total RNA was isolated from LNCaP cells treated with 2.5 µM and 5 µM of SAHA for 8, 16 and 24...
<p>A) Western blot analysis of SREBP2 protein levels in SH-SY5Y cells after treatment with 250 nM TS...
Abstract Background Epithelial-mesenchymal transition (EMT) may be one of the reasons for the failur...
Background: Cancer stem cells (CSCs) play a key role in cancer initiation, progression and chemoresi...
<p>(A) Western blot analysis depicting increased BMI-1 expression in HNSCC cells following TSA treat...
<p>(A) FaDu, Cal-27, and Hep-2 cells were treated with indicated concentrations of DHA for 24 or 48h...
<p>(A) <i>BLM</i> and (B) <i>XPA</i> human lymphocytes were treated with 0 to 1.5 µM TSA or 0 to 100...
<p><b>A</b>. Apoptosis of PBMCs, PBLs, and monocytes from healthy controls after treatment with TSA ...
<p>(A and B) PC3 cells treated with TSA and SAHA for 24 h at indicated doses. The photomicrographs o...
<p>(A) Total RNA was isolated from LNCaP cells treated with 200 nM and 400 nM TSA for 8, 16 and 24 h...
<p>(A) CHIP assay was conducted to determine the binding of HDACs and acetylation status of histone ...
<p>Total RNA was isolated from PC3 cells treated with 200 nM and 400 nM TSA (A) or 2.5 µM and 5 µM S...
<p>SGC-996 cells were treated with or without different concentrations of TSA or SAHA for 24 h. The ...
Clinical experience of histone deacetylase inhibitors (HDACIs) in patients with solid tumors has bee...
<p>A–B: TSA treatment caused increased expression of TGF-α. Myofibroblasts were treated with theo (t...
<p>(A) Total RNA was isolated from LNCaP cells treated with 2.5 µM and 5 µM of SAHA for 8, 16 and 24...
<p>A) Western blot analysis of SREBP2 protein levels in SH-SY5Y cells after treatment with 250 nM TS...
Abstract Background Epithelial-mesenchymal transition (EMT) may be one of the reasons for the failur...
Background: Cancer stem cells (CSCs) play a key role in cancer initiation, progression and chemoresi...
<p>(A) Western blot analysis depicting increased BMI-1 expression in HNSCC cells following TSA treat...
<p>(A) FaDu, Cal-27, and Hep-2 cells were treated with indicated concentrations of DHA for 24 or 48h...
<p>(A) <i>BLM</i> and (B) <i>XPA</i> human lymphocytes were treated with 0 to 1.5 µM TSA or 0 to 100...
<p><b>A</b>. Apoptosis of PBMCs, PBLs, and monocytes from healthy controls after treatment with TSA ...