2C) Concordantly, SIRT2 depletion reduced DNA synthesis by 50% (

2C). Concordantly, SIRT2 depletion reduced DNA synthesis by 50% (P < 0.001), as measured by BrdU incorporation assay (Fig. 2D). Cell-cycle distribution, as determined by FACS analysis, revealed that SIRT2 silencing significantly induced G1 and G2 arrest Dabrafenib purchase in p53 WT (SK-Hep-1 and HepG2) and in p53-mutated (Huh-7 and PLC5) cells, respectively

(Fig. 2E). Nevertheless, unlike the knockdown of SIRT1,23 knockdown of SIRT2 neither resulted in cellular senescence nor apoptosis of HCC cells (data not shown). Taken together, these data suggested that SIRT2 depletion might inhibit cell growth by inducing cell-cycle delay. Next, we evaluated whether SIRT2 plays a role in the motility of HCC cells. Depletion of SIRT2 (shSIRT2-1 and shSIRT2-2), but not SIRT1 (shSIRT1-1), markedly reduced cell migration through transwell (P < 0.01) (Fig. 3A). Concordantly, knockdown of SIRT2 also diminished wound-healing capacity (P < 0.01) (Fig. 3B) and impaired cell invasion through Matrigel (P < 0.01) (Fig. 3C). In contrast, ectopic expression of WT SIRT2 promoted migration and invasion capacity in

L02 cells (Fig. 3D). Together, these data suggested a role of SIRT2 in the motility and invasiveness VX-770 in vivo of HCC cells. EMT, the sequence of events that converts adherent epithelial cells into migratory cells, which invade the extracellular matrix,28 is associated with tumor metastasis.29 Therefore, we determined whether EMT is responsible for SIRT2-mediated change in cell motility. Knockdown of SIRT2 in HCC cells induced the expression of epithelial markers E-cadherin and α-catenin that was accompanied by a concomitant reduction of

mesenchymal marker N-cadherin and α-SMA. Nevertheless, the expression of vimentin, another mesenchymal marker, was not altered (Fig. 3E). F-actin distribution was also rearranged in SIRT2-depleted cells from a stress-fiber to a cortical pattern, suggestive of a conversion to the epithelial phenotype (Fig. 3F). Therefore, our data suggest a loss of mesenchymal-like features and reacquisition 4��8C of epithelial characteristics in SIRT2-depleted HCC cells. The role of SIRT2 in EMT was further supported by the reduced expression of E-cadherin and alpha-catenin, as well as the enhanced expression of N-cadherin and α-SMA in L02 cells, which SIRT2 was ectopically expressed (Fig. 3E). Reduced expression of E-cadherin and the activation of WNT signaling lead to the accumulation and nuclear import of β-catenin, where it interacts with TCF/LEF to induce the expression of genes responsible for the EMT process.30, 31 Therefore, we have elucidated whether SIRT2 plays a role in β-catenin signaling or not. Expression of SIRT2 shRNAs in SK-Hep1 and Huh7 cells markedly reduced the level of the total, as well as the active (dephosphorylated on Ser37 and Ser41), β-catenin (Fig. 4A).

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