er cells compared with control cells. To further examine the role of NF ��B in EMT of gastric cancer cells, we analyzed the effect of NF ��B inhibition on the expressions of representative EMT marker pro teins. Immunoblotting showed that the expression of E cadherin, a representative epithelial marker, increased, whereas the expression of mesenchymal markers Snail selleck chemicals and MMP9 decreased after I��BM overexpression. STAT3 silencing decreases the migration and invasion through regulation of EMT markers Next, we confirmed the effects of STAT3 silencing on the motility and invasiveness in gastric cancer cells. As expected from the previous report, STAT3 silencing suppressed cell migration compared with control siRNA transfected gastric cancer cells. Moreover, STAT3 silencing also decreased invasiveness compared with control cells.

We found that E cadherin increased, whereas Snail and MMP9 decreased after transfection of STAT3 siRNA. NF ��B and STAT3 cooperatively induce migration and invasion of gastric cancer cells Our results in the present study showed that NF ��B and STAT3 played important roles in migration and invasion, and that NF ��B was an upstream regulator of STAT3. To examine the combined effect of NF ��B and STAT3 on the metastatic potential of gastric cancer cells, we per formed co transfection of I��BM and STAT3 siRNA into SNU 638 cells. To confirm the effects of co transfection of I��BM and STAT3 siRNA on expression of pRelA and pSTAT3, we obtained whole cell lysates and nuclear extracts and performed immunoblotting.

We found that double knock down of RelA and STAT3 induced marked down regulation of pSTAT3 expression in both the whole cell lysates and nuclear extracts. In quantitative terms, the migration capacity decreased by 50% in I��BM overexpressing AV-951 cells, and by 45% in STAT3 slienced cells compared with control cells. In the co transfected cells, the migration capacity was remark ably inhibited when STAT3 was further silenced. Similarly, invasion assay showed that cells with down regulation of both NF ��B and STAT3 showed lower invasion abil ity than those with down regulation of either alone. These data suggest that STAT3 in this system is induced not only through NF ��B, but also through something else. It is known that STAT3 pathway can be induced by many NF ��B independent pathways including some cytokines and tyrosine kinases.

We also found that E cadherin expression was increased whereas Snail ex pression was decreased in cells with down regulation of both NF ��B and STAT3 compared with those with down regulation of either alone. Discussion Understanding of a clear regulatory path of signaling molecules in cancer cells is a pre requisition to successful co development of therapeutic targets for tumors. selleck bio Since the pivotal role of NF ?B in gastric cancer progression has been shown, a thorough understanding of NF ?B pathway can lead to future studies and drug development which could provide a novel option in the treatment of this disease. Althou