Abstract

This study investigated the role of curcumin nanocarriers carrying TAR-RNA binding protein (TRBP) in hepatocellular carcinoma (HCC). We conducted a retrospective analysis of 60 HCC tissue samples and 30 normal liver tissues. TRBP level was measured in HCC. Disease-free survival (DFS) and overall survival (OS) were calculated to analyze correlation between TRBP expression and diagnostic sensitivity of HCC. Survival factors were analyzed using cyclo-oxygen-ase (COX) univariate and multivariate survival analysis. The curcumin nanocarriers-loaded siRNA (si)-TRBP were transfected into HCC cells during in vitro experiments to detect HCC cell proliferation and invasion, whilst flow cytometry measured apoptosis rate of cancer cells. TRBP was highly expressed in 60 HCC tissues and positively associated with diagnostic sensitivity of HCC, with lower DFS and OS in HCC patients with higher TRBP expression, and FIGO stage and TRBP were indicated as risk factors for DFS and OS. High TRBP expression coexisted with increased HCC cell proliferation and invasion. Moreover, transfection of curcumin nanocarriers-loaded si-TRBP dramatically decreased cell viability and invasion, downregulated cleaved caspase-3 and caspase-9, while upregulating Bcl-2. Collectively, this study demonstrated TRBP is upregulated in HCC and curcumin nanocarriers carrying si-TRBP, significantly suppressing growth of HCC cells, providing a theoretical basis for treatment of HCC.

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