Gth HOXD10 cDNA (GenBank accession number NM_002148.3) was cloned into the pcDNA3.1 expression vector. Transient

Gth HOXD10 cDNA (GenBank accession number NM_002148.3) was cloned into the pcDNA3.1 expression vector. Transient transfection was performed using Lipofectamine 3000 (Intrivogen, Carlsbad, CA) according to the manufacturer’s instructions.Cell viability detectionHCC cell lines were split to a low density (30 confluence) 12 h before treatment. Cells were treated with 5-aza-2deoxycytidine (5-aza) (Sigma, St. Louis, MO) at a concentration of 2 M. Growth medium conditioned with 5-aza at a concentration of 2 M was exchanged every 24 h for a total of 96 h of treatment.RNA isolation and semi-quantitative RT-PCRCells were plated into 96-well plates at a density of 2 ?103 cells/well, and cell viability was measured by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay (KeyGEN Biotech, Nanjing, China) at 0, 24, 48, and 72 h. Absorbance was measured using a microplate reader (Thermo Peretinoin site Multiskan MK3, MA, USA) at a wavelength of 490 nm.Colony formation assayTotal RNA was isolated by Trizol reagent (Life Technologies, Gaithersburg, MD). First-strand cDNA was synthesized according to the manufacturer’s instructions (Invitrogen, Carlsbad, CA). PCR primers for HOXD10 are listed in Additional file 1: PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/27906190 Table S1. The primer sets for HOXD10 were designed to span intronic sequences between adjacent exons in order to control for genomic DNA contamination. RT-PCR was amplified for 33 cycles. GAPDH was amplified for 25 cycles as an internal control.Bisulfite modification, methylation-specific PCR (MSP), and bisulfite sequencingCells were seeded into 6-well culture plates at a density of 800 cells per well in triplicate and cultured for 2 weeks. For Huh7 and SMMC7721 cells, growth medium was conditioned with G418 (Invitrogen, Carlsbad, CA) at 300 and 50 g/ml, respectively, and was exchanged every 24 h. Cells were then fixed with 75 ethanol for 30 min, stained with 0.2 crystal violet (Beyotime, Nanjing, China) for 20 min and counted.Flow cytometryDNA was prepared by the proteinase K method. Bisulfite treatment was carried out as previously described [19]. MSP primers were designed according to genomicFor cell cycle analysis, cells were serum starved 12 h for synchronization and then re-stimulated with 10 FBS for 24 h. Cells were fixed with 70 ethanol and prepared for cell cycle detection using the Cell Cycle Detection Kit (KeyGen Biotech, Nanjing, China). Cells were then sorted by a FACSCalibur (BD Biosciences, San Jose, CA) and analyzed by the Modfit software (Verity Software House, ME, USA). For apoptosis analysis, the Annexin VFITC/PI Apoptosis Detection Kit (KeyGen Biotechnology,Guo et al. Clinical Epigenetics (2017) 9:Page 3 ofChina) was used according to manufacturer’s instructions. Each sample was analyzed by flow cytometry with a FACScan Flow Cytometer (Becton-Dickinson Biosciences, Mansfield, MA).Transwell assayIL, USA), cleaved caspase 3 (Protein Tech Group, Chicago, IL, USA), and -actin (Bioworld Tech, MN, USA).HOXD10 unexpressed and re-expressed SMMC7721 cell xenograft mouse modelCells were suspended in serum-free medium. Cells (2 ?104) were placed into the upper chamber of an 8m pore size transwell apparatus (Corning, NY, USA) and incubated for 24 h. Cells that migrated to the lower surface of the membrane were stained with crystal violet and counted in three independent high-power fields (?00). For invasion analysis, cells (3 ?104) were seeded into the upper chamber of a transwell apparatus coated with Matrigel (BD Bioscien.