By 2DE and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry mass spectral measurement, a total of eight proteins were differentially expressed in CHD1L-transfected QGY-7703 cells (CHD1L-7703), when compared to empty vector-transfected cells (Vec-7703) (Supporting Fig. 1A; Supporting Table 1). Further validations suggested that TCTP might be a target gene of CHD1L (Supporting Fig. 1B,C). As reported by our previous study, CHD1L possesses a DNA-binding activity with a putative DNA-binding

motif (C/A)C(T/A)T(T/A/G)T,12 and CHD1L may, therefore, up-regulate TCTP expression through a protein-DNA interaction. Using the MatInspector Professional software Dabrafenib molecular weight (Genomatrix Software GmbH, Munich, Germany)13, 14 to search for a CHD1L-binding site within a 1.8-kb upstream region of

TCTP, two CHD1L-binding sites were identified at −748 bp (base pairs) and −851 bp in the 5′-flanking region of TCTP (Fig. 1A). By using the ChIP-PCR OSI-906 manufacturer assay, we found that only DNA Fragment C (nt −733/−1027) containing two CHD1L-binding motifs, but not Fragment A (nt +91/−213) and Fragment B (nt −195/−500), could be detected in CHD1L-ChIPed DNA fragments (Fig. 1B). Supershift signal was only observed in the lane containing DIG-labeled Fragment C, nuclear extract of GFP/CHD1L-7703-C3 cells, and anti-GFP antibody (lane 11) (Fig. 1C). Luciferase reporter assay was used to further confirm that CHD1L could activate TCTP transcription. As a result, luciferase activity of pGL3-TCTP-FD was significantly increased in

cells cotransfected with pcDNA3.1-CHD1L, but not with pcDNA3.1 (P < 0.05), whereas the luciferase activities of pGL3-TCTP-FA, FB, and FC were not increased in cells cotransfected with pcDNA3.1-CHD1L (Fig. 1D). These results demonstrated that CHD1L could bind to the CHD1L-binding motifs within the 5′-upstream region (nt −733/−1027) selleck screening library of TCTP and activate TCTP transcription; however, the other sequence (Fragment A: nt +91/−213) of the 5′-upstream region was also required for the activation of TCTP transcription. Protein expression of TCTP and CHD1L was detected in seven cell lines, including six HCC cell lines and one immortalized human liver cell line (LO-2). TCTP expression was positively correlated with that of CHD1L in these seven cell lines (Spearmen correlation coefficient, 0.786; P = 0.048) (Supporting Fig. 2A-C). Serial sections of 5 HCCs with surrounding nontumor tissues were stained with antibodies against CHD1L and TCTP. As a result, the expression patterns of TCTP and CHD1L showed almost perfect concordance in both tumor and nontumor tissues (Supporting Fig. 2D). Furthermore, PLC8024 and Huh7 cells were treated with short interfering RNA (siRNA) against CHD1L (siCHD1L) or the corresponding scrambled siRNA. As detected by quantitative PCR (qPCR), siCHD1L-treated cells showed the lower expression of both CHD1L and TCTP than that of the scrambled siRNA-treated cells (P < 0.0001 and P < 0.00001; Fig.