{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["9(13)"],"submitter":["Jilkova ZM"],"pubmed_abstract":["The prognosis of patients with advanced hepatocellular carcinoma (HCC) is very poor. The AKT pathway is activated in almost half of HCC cases and in addition, long term exposure to conventional drug treatment of HCC, sorafenib, often results in over-activation of AKT, leading to HCC resistance. Therefore, it is important to assess the safety and the efficacy of selective allosteric AKT inhibitor ARQ 092 (Miransertib) in combination with sorafenib. Here, we demonstrated <i>in vitro</i> that the combination of ARQ 092 with sorafenib synergistically suppressed proliferation, promoted apoptosis, and reduced migration. To test the effect of the combination <i>in vivo</i>, rats with diethylnitrosamine-induced cirrhosis and fully developed HCC were randomized and treated with vehicle, sorafenib, "],"journal":["Oncotarget"],"pagination":["11145-11158"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC5834253"],"repository":["biostudies-literature"],"pubmed_title":["Combination of AKT inhibitor ARQ 092 and sorafenib potentiates inhibition of tumor progression in cirrhotic rat model of hepatocellular carcinoma."],"pmcid":["PMC5834253"],"pubmed_authors":["Roth GS","Sturm N","Hainaut P","Abbadessa G","Schwartz B","Kurma K","Kuyucu AZ","Ahmad Pour ST","Marche PN","Decaens T","Jilkova ZM","Yu Y"],"additional_accession":[]},"is_claimable":false,"name":"Combination of AKT inhibitor ARQ 092 and sorafenib potentiates inhibition of tumor progression in cirrhotic rat model of hepatocellular carcinoma.","description":"The prognosis of patients with advanced hepatocellular carcinoma (HCC) is very poor. The AKT pathway is activated in almost half of HCC cases and in addition, long term exposure to conventional drug treatment of HCC, sorafenib, often results in over-activation of AKT, leading to HCC resistance. Therefore, it is important to assess the safety and the efficacy of selective allosteric AKT inhibitor ARQ 092 (Miransertib) in combination with sorafenib. Here, we demonstrated <i>in vitro</i> that the combination of ARQ 092 with sorafenib synergistically suppressed proliferation, promoted apoptosis, and reduced migration. To test the effect of the combination <i>in vivo</i>, rats with diethylnitrosamine-induced cirrhosis and fully developed HCC were randomized and treated with vehicle, sorafenib, ","dates":{"release":"2018-01-01T00:00:00Z","publication":"2018 Feb","modification":"2025-04-19T15:18:02.553Z","creation":"2019-03-26T23:17:49Z"},"accession":"S-EPMC5834253","cross_references":{"pubmed":["29541403"],"doi":["10.18632/oncotarget.24298"]}}