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staining showed reduced angiogenesis in combination group compared to the control
          (p<0.0001) or sorafenib group (p<0.0001) with significantly decreased HIF expression
          in tumor tissues. The results from Sirius red staining showed a decrease in fibrosis of
          animals treated with ARQ 092 alone (p=0.0004) or with combination of ARQ 092 and
          sorafenib (p=0.0001), accompanied with strong downregulation of TGFB, Collagen1 and
          ACTA1 expression levels. Granulocyte/T-cells ratio in blood was decreased in all treated
          groups compared to the control group and accumulation of neutrophils in liver tissue was
          significantly reduced. Western blot analysis of liver tissues showed a significant reduction
          of phosphorylation of AKT and its downstream signalling actors mTOR and S6K1 in
          both ARQ 092 and combination groups.

          Conclusions: Combination of  ARQ 092 and sorafenib exerted additive effect in
          controlling tumor progression and improved immune response in blood and liver. Our
          results confirm the importance of targeting AKT in HCC.
          Figure:




        ePOSTER ABSTRACTS

















          Disclosure of Interest: Z. Macek Jilkova: : None Declared, A. Zeybek Kuyucu: : None
          Declared, K. Kurma: : None Declared, S. T. Ahmad Pour: : None Declared, G. Roth: :
          None Declared, G. Abbadessa: Employee: Conflict with: ArQule Inc, Y. Yu: Employee:
          Conflict with: ArQule Inc, V. Leroy: : None Declared, P. Marche: : None Declared, T.
          Decaens: : None Declared








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