亚洲传统医药 ›› 2024, Vol. 19 ›› Issue (4): 177-191.

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Network pharmacology to decipher the mechanism of Danggui  Longhui Wan against chronic myeloid leukemia

  

  • 出版日期:2024-09-19 发布日期:2024-09-19

Network pharmacology to decipher the mechanism of Danggui  Longhui Wan against chronic myeloid leukemia

  • Online:2024-09-19 Published:2024-09-19

摘要:

Chronic myeloid leukemia (CML) is a hematopoietic myeloproliferative disorder. The Chinese prescription Danggui Longhui  Wan (DGLHW) has been utilized in CML treatment, but its underlying mechanisms remain unclear. In this study, we gathered 794 constituents, 1249 drug targets, 1654 disease genes and 129 intersection genes. GO and KEGG were used to analyze the  function of these genes. Compatibility of prescription study showed that monarch drug, minister drug, assistant and guide drug  played a synergistic role in the treatment of CML. In addition, we obtained 20 hub genes and 12 key components. Molecular  docking indicated that the main compounds and core proteins had good binding ability. The results of this study also showed that  DGLHW might play a role in the treatment of CML by affecting MAPK, PI3K/AKT, FoxO and p53 signaling pathways.

关键词: chronic myeloid leukemia, Danggui Longhui Wan, network pharmacology, compatibility analysis

Abstract:

Chronic myeloid leukemia (CML) is a hematopoietic myeloproliferative disorder. The Chinese prescription Danggui Longhui  Wan (DGLHW) has been utilized in CML treatment, but its underlying mechanisms remain unclear. In this study, we gathered 794 constituents, 1249 drug targets, 1654 disease genes and 129 intersection genes. GO and KEGG were used to analyze the  function of these genes. Compatibility of prescription study showed that monarch drug, minister drug, assistant and guide drug  played a synergistic role in the treatment of CML. In addition, we obtained 20 hub genes and 12 key components. Molecular  docking indicated that the main compounds and core proteins had good binding ability. The results of this study also showed that  DGLHW might play a role in the treatment of CML by affecting MAPK, PI3K/AKT, FoxO and p53 signaling pathways.

Key words: chronic myeloid leukemia, Danggui Longhui Wan, network pharmacology, compatibility analysis