Title : Combined Inhibition of TGF-β1-Induced EMT and PD-L1 Silencing Re-Sensitizes Hepatocellular Carcinoma to Sorafenib Treatment.

Pub. Date : 2021 Apr 27

PMID : 33925488






5 Functional Relationships(s)
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1 The effect of combination treatment with SB431542, a specific inhibitor of the transforming growth factor (TGF)-beta receptor kinase, and siRNA mediated knockdown of programmed cell death protein ligand-1 (PD-L1) on Sorafenib resistance was examined using a cell viability assay. Sorafenib CD274 molecule Homo sapiens
2 The effect of combination treatment with SB431542, a specific inhibitor of the transforming growth factor (TGF)-beta receptor kinase, and siRNA mediated knockdown of programmed cell death protein ligand-1 (PD-L1) on Sorafenib resistance was examined using a cell viability assay. Sorafenib CD274 molecule Homo sapiens
3 Following Sorafenib exposure, increase in the expression of PD-L1 and other immune checkpoints was observed. Sorafenib CD274 molecule Homo sapiens
4 Moreover, the sensitivity of HCC cells to Sorafenib was enhanced by combining a blockade of EMT with SB431542 and knockdown of PD-L1 expression. Sorafenib CD274 molecule Homo sapiens
5 Sorafenib-induced motility was attenuated with the combined treatment of SB431542 and PD-L1 knockdown. Sorafenib CD274 molecule Homo sapiens