Yu-Ping-Feng-San improve the immunosuppression of microenvironment in hepatocellular carcinoma by promoting the maturation of DCs through the JAK2-STAT3 pathway

Sci Rep. 2024 Dec 28;14(1):31522. doi: 10.1038/s41598-024-83197-7.

Abstract

Yu-Ping-Feng-San (YPF) is a famous classical Chinese medicine formula known for its ability to boost immunity. YPF has been applied to enhance the immune status of tumor patients in clinical practice. However, there is still a lack of research on its immune regulatory effects and mechanisms in the tumor microenvironment. This study was designed to investigate the effects and mechanism of YPF on improving the immune suppression state of hepatocellular carcinoma (HCC) microenvironment. In an orthotopic mouse model of HCC, YPF improved the immune microenvironment of HCC immunosuppression, enhanced the maturation of dendritic cells (DCs), promoted the release of IL-12, and decreased the presence of JAK2, p-JAK2, STAT3, and p-STAT3 proteins in both tumor tissue and paracancerous tissues. YPF also could promote the maturation and reduce the activation of JAK2, p-JAK2, STAT3, and p-STAT3 proteins of mouse bone marrow-derived DCs induced by culture medium or tumor supernatant in vitro. Transient transfection of siRNA-STAT3 with DCs resulted in an increase in its maturation and its secretion of IL-12. On the whole, these combined effects of YPF served to ameliorate the HCC immune suppression microenvironment, which conducive to immune cells play the role of immune surveillance and killing liver cancer cells. The mechanisms of these combined effects were, at least in part, related to its inhibition of the activated JAK2-STAT3 signaling pathway in DCs within the HCC microenvironment.

Keywords: Dendritic cells; Hepatocellular carcinoma; Immune microenvironment; JAK2-STAT3 pathway; Yu-Ping-Feng-San.

MeSH terms

  • Animals
  • Carcinoma, Hepatocellular* / drug therapy
  • Carcinoma, Hepatocellular* / immunology
  • Carcinoma, Hepatocellular* / metabolism
  • Carcinoma, Hepatocellular* / pathology
  • Cell Line, Tumor
  • Dendritic Cells* / drug effects
  • Dendritic Cells* / immunology
  • Dendritic Cells* / metabolism
  • Drugs, Chinese Herbal* / pharmacology
  • Humans
  • Immunosuppression Therapy
  • Interleukin-12 / metabolism
  • Janus Kinase 2* / metabolism
  • Liver Neoplasms* / drug therapy
  • Liver Neoplasms* / immunology
  • Liver Neoplasms* / metabolism
  • Liver Neoplasms* / pathology
  • Male
  • Mice
  • STAT3 Transcription Factor* / metabolism
  • Signal Transduction* / drug effects
  • Tumor Microenvironment* / drug effects

Substances

  • Janus Kinase 2
  • STAT3 Transcription Factor
  • Drugs, Chinese Herbal
  • Interleukin-12
  • Jak2 protein, mouse
  • JAK2 protein, human