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ABSTRACT: Background
Targeted therapies for Primary liver cancer (HCC) is limited to the multi-kinase inhibitors, and not fully effective due to the resistance to these agents because of the heterogeneous molecular nature of HCC developed during chronic liver disease stages and cirrhosis. Although combinatorial therapy can increase the efficiency of targeted therapies through synergistic activities, isoform specific effects of the inhibitors are usually ignored. This study concentrated on PI3K/Akt/mTOR pathway and the differential combinatory bioactivities of isoform specific PI3K-α inhibitor (PIK-75) or PI3K-β inhibitor (TGX-221) with Sorafenib dependent on PTEN context.Methods
The bioactivities of inhibitors on PTEN adequate Huh7 and deficient Mahlavu cells were investigated with r
SUBMITTER: Narci K
PROVIDER: S-EPMC8953069 | biostudies-literature | 2022 Mar
REPOSITORIES: biostudies-literature