These results indicate that Gs activates PP2A by phosphorylating the B56 subunit

Therefore, it is unclear at present whether ABT 263 enhanced Mcl 1 mRNA stability is associated with CUGBP2, which is interesting and needs further studies. Besides mRNA level, protein stability also plays im portant role in the upregulation of Mcl 1 protein. It is known that the phosphorylation of Mcl ARN509 1 is closely asso ciated with Mcl 1 protein stabilization. Serine159 and Threonine163 are two important phosphorylation sites in Mcl 1 PEST region to determine the fate of Mcl 1 degradation. Mcl 1 can be phosphorylated by ERK at its Thr163 site, which prolongs the half life of this protein. ERK mediated phosphorylation at Thr163 repre sents an important resistant mechanism in leukemia cells and the inhibition of MEKERK sensitizes the anti tumor effect of ABT 737.<br><br> Consistent with these reports, our study showed that ERK mediated Thr163 phosphorylation of Mcl 1 contributed to ABT 263 resist ance in HCC cells. JNK, another important member of MAPK family, can phosphorylate Mcl 1 at several sites, but the effect of JNK on Mcl 1 is varied. JNK mediated Thr163 phosphorylation AT7519 ic50 may lead to enhanced Mcl 1 degradation or increased Mcl 1 stabilization. Our data demonstrated that ABT 263 increased JNK mediated Mcl 1Thr163 phosphorylation, which enhanced Mcl 1 protein stability in HCC cells. Furthermore, both ERK and JNK inhibitors sensitized ABT 263 induced apoptosis and cell death by downregulating Mcl 1 in HCC cells, which may be novel ways to sensitize ABT 263 in HCC therapy. GSK 3B plays an important role in glucose metabolism in mammalian cells.<br><br> After being phosphorylated at Serine9, GSK supplier Alisertib 3B loses its activity. It is known that Mcl 1 can be phosphorylated by GSK 3B at Ser159 site, which decreases Mcl 1 stability. A recent study has shown that ABT 263 enhances the anti tumor effect of PI3K in hibitor in GSK3 dependent manner in human myeloid leukemia cells, but the detailed mechanisms are still not clear. Our study demonstrated that ABT 263 pro moted GSK 3B inactivation and Mcl 1 stability via Akt pathway, indicating that inhibition of Akt may be a good strategy to sensitize ABT 263 in HCC treatment. It is well known that Bcl 2xL are involved in regulat ing the homeostasis of apoptosis, autophagy and oxida tive stress in the cells, which are associated with ERK, JNK and Akt pathways. ABT 263 is known as a specific inhibitor of Bcl 2xL, so the mechanisms by which ABT 263 activates ERK, JNK and Akt may be complicated.<br><br> Our previous data have shown that Bcl 2 inhibitor apogossypolone can induce reactive oxygen species in HCC cells, which results in the activa tion of multiple vital signaling pathways including ERK, JNK and Akt pathways. In the present study, we demonstrated that ABT 263 could induce the phosphory lations of ERK, JNK and Akt, which were markedly atten uated by the widely used antioxidant N acetyl cysteine, suggesting that ABT 263 may activates ERK, JNK and Akt via, at least partially, inducing ROS production. Conclusions In conclusion, our study demonstrates that ABT 263 upregulates Mcl 1 through increasing its mRNA and protein stability, which contributes to the resistance of ABT 263 in HCC cells.