Publication | Closed Access
18β‐glycyrrhetinic acid inhibits hepatocellular carcinoma development by reversing hepatic stellate cell‐mediated immunosuppression in mice
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Citations
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References
2012
Year
GlycobiologyImmunologyPathologyImmune RegulationImmunologic MechanismImmunotherapeuticsImmunotherapyTumor BiologyHcc DevelopmentTumor ImmunityCancer Cell BiologyHepatic StellateHepatotoxicityCancer ResearchHcc Cell InvasivenessLiver PhysiologyImmunoengineeringImmune SurveillanceT Cell ImmunityCell BiologyTumor MicroenvironmentCancer ImmunosurveillanceHepatologyLiver DiseaseLiver CancerCellular Immune ResponseLiverMedicineHcc TherapyHepatocellular Carcinoma
Abstract Hepatic stellate cells (HSCs) have immunosuppressive capabilities and contribute to the occurrence and development of hepatocellular carcinoma (HCC). Thus, activated HSCs may be a suitable target for HCC therapy. Our study used mixed leukocyte reactions (MLR) in vitro to demonstrate that 18β‐glycyrrhetinic acid (GA) could reverse HSC‐mediated immunosuppression by reducing T‐cell apoptosis and regulatory T (Treg) cells expression, thereby enhancing the ability of T cells to attack tumor cells and attenuating HCC cell invasiveness. Moreover, we established a HCC orthotopic implantation model in immunocompetent C57BL/6 mice, which suggested that GA played a protective role in HCC development by reducing immunosuppression mediated by HSCs in the tumor microenvironment.
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