A previous study demonstrated that the duration and intensity of JNK activation are associ ated with apoptotic cell death and that Bad dephosphoryla tion is accompanied by increases in JNK phosphorylation and activity. Moreover, JNK activation leads to inacti vation of the survival functions of Bcl 2 through Bcl 2 phosphorylation. In this study, Bad dephosphorylation and Bcl 2 phosphorylation with an elevation of JNK phos phorylation were induced by doceta el, suggesting that JNK positively regulates apoptosis induction through Bad dephosphorylation and Bcl 2 phosphorylation. Conclusions In summary, this study demonstrated that Vav3 mediated signaling converges with PI3K Akt, ERK, and AR signaling pathways in support of the growth and survival of prostate cancer cells under chronic hypo ia.

Because the pAR positive cell ratio was not found to be associated with apoptosis and tumor growth delay in in vivo analysis, LNCaPH cell growth appeared to be regulated by Inhibitors,Modulators,Libraries both AR dependent and AR independent pathways. Therefore, si Vav3, which targets the PI3K Akt, ERK, and AR signal ing a is, was effective when combined with doceta el, which targets Bcl 2 and Bad. Increased Bad and AR phos phorylation by the activation of PI3K Akt and ERK signal ing pathways upon Vav3 stimulation contributes to prostate cancer growth under chronic Inhibitors,Modulators,Libraries hypo ia, whereas increased Bcl 2 phosphorylation and decreased Bad phosphorylation through the activation of JNK signal ing by doceta el coupled with decreased phosphorylation of Bad and AR through the inhibition of PI3K Akt and ERK signaling pathways upon the addition of si Vav3 con tributes to AV-951 increased apoptosis.

The present study describes a potentially useful approach of utilizing the combination of doceta el and si Vav3 to enhance the apoptosis of Inhibitors,Modulators,Libraries prostate cancer cells under chronic hypo ia. In addition, doceta el plus si Vav3 e hibited no to icity in mice, which makes it an attractive and safe therapeutic strategy in future clinical application to treat prostate cancer. This approach may provide a novel strategy for the treatment of HRPC, particularly advanced prostate Inhibitors,Modulators,Libraries cancer in which the Vav3 signaling pathway is activated. Methods Cell culture and hypo ia induction LNCaP human prostate cancer cells were maintained in RPMI 1640 medium supplemented with 10% heat inactivated fetal bovine serum, 50 IU ml penicillin, and 50 ug ml streptomycin and cul tured at 37 C in a humidified atmosphere of 5% CO2.

To establish chronic hypo ia conditioned LNCaP cells, LNCaP cells were cultured under hypo ia for 6 months. The e periments using LNCaPH cells were performed under hypo ic conditions. KPK13 human renal cell carcinoma cells were cultured in minimum essential medium supplemented with 10% FBS, with 50 IU ml penicillin, and 50 ug ml streptomycin in 5% CO2 at 37 C.