Anti-tumor effects and immuno-inflammatory-metabolic mechanisms of Buzhong Yiqi Granules in improving cancer-related fatigue in lung cancer.
[OBJECTIVE] To investigate the anti-tumor effects and immuno-inflammatory-metabolic mechanisms of Buzhong Yiqi Granules (BYG) in alleviating cancer-related fatigue (CRF) in lung cancer.
APA
Mei S, Peng S, et al. (2026). Anti-tumor effects and immuno-inflammatory-metabolic mechanisms of Buzhong Yiqi Granules in improving cancer-related fatigue in lung cancer.. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 34(4). https://doi.org/10.1007/s00520-026-10618-w
MLA
Mei S, et al.. "Anti-tumor effects and immuno-inflammatory-metabolic mechanisms of Buzhong Yiqi Granules in improving cancer-related fatigue in lung cancer.." Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, vol. 34, no. 4, 2026.
PMID
41915246
Abstract
[OBJECTIVE] To investigate the anti-tumor effects and immuno-inflammatory-metabolic mechanisms of Buzhong Yiqi Granules (BYG) in alleviating cancer-related fatigue (CRF) in lung cancer.
[METHODS] UPLC-Q-TOF/MS detected compounds in BYG. CRF was induced in mice via Lewis lung carcinoma cell inoculation, with daily BYG treatment for 14 days. Anti-fatigue efficacy was evaluated through behavioral tests and ATP content detection. Anti-tumor effects were assessed via histopathology, tumor volume, and weight. Immuno-inflammatory-metabolic mechanisms were evaluated using inflammatory cytokines (IL-6, TNF-α, IFN-γ) and immune cell subsets (CD4+, CD8+ T cells) in serum and tumor tissues.
[RESULTS] Ninety-four active compounds were identified in BYG. In the CRF mouse model, BYG prolonged swimming time, reduced tail suspension immobility, increased muscle ATP to exert anti-fatigue effects; it inhibited tumor growth and metastasis by reducing volume and downregulating EGFR/CD34/MMP-9; it also modulated inflammation and immunity by lowering IL-6/TNF-α, elevating IFN-γ, enhancing CD4 + T cells and restoring the CD4 + /CD8 + ratio.
[CONCLUSIONS] BYG alleviates CRF via multi-target mechanisms involving energy metabolism, tumor inhibition, and immune-inflammatory regulation, supporting its clinical use in CRF and potential as lung cancer adjuvant therapy.
[METHODS] UPLC-Q-TOF/MS detected compounds in BYG. CRF was induced in mice via Lewis lung carcinoma cell inoculation, with daily BYG treatment for 14 days. Anti-fatigue efficacy was evaluated through behavioral tests and ATP content detection. Anti-tumor effects were assessed via histopathology, tumor volume, and weight. Immuno-inflammatory-metabolic mechanisms were evaluated using inflammatory cytokines (IL-6, TNF-α, IFN-γ) and immune cell subsets (CD4+, CD8+ T cells) in serum and tumor tissues.
[RESULTS] Ninety-four active compounds were identified in BYG. In the CRF mouse model, BYG prolonged swimming time, reduced tail suspension immobility, increased muscle ATP to exert anti-fatigue effects; it inhibited tumor growth and metastasis by reducing volume and downregulating EGFR/CD34/MMP-9; it also modulated inflammation and immunity by lowering IL-6/TNF-α, elevating IFN-γ, enhancing CD4 + T cells and restoring the CD4 + /CD8 + ratio.
[CONCLUSIONS] BYG alleviates CRF via multi-target mechanisms involving energy metabolism, tumor inhibition, and immune-inflammatory regulation, supporting its clinical use in CRF and potential as lung cancer adjuvant therapy.
MeSH Terms
Animals; Fatigue; Drugs, Chinese Herbal; Mice; Mice, Inbred C57BL; Carcinoma, Lewis Lung; Lung Neoplasms; Male; Cytokines; Disease Models, Animal; Adenosine Triphosphate