Pakistan journal of pharmaceutical sciences · 2026
Effects of curcumin on the signal transducer and activator of transcription 3 signaling pathway and bile acid enterohepatic circulation in liver cancer mice model.
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Hu Na, Yan Niu, Zhao Tingting, Hu Langui
Аннотация
BACKGROUND: Liver cancer has a high incidence and poor prognosis. Curcumin is a natural compound with anti-tumor activity, but its effects on the STAT3 signaling pathway and the bile acid enterohepatic circulation in liver cancer models remain unclear.
OBJECTIVES: To investigate the effects of curcumin on the STAT3 signaling pathway and bile acid enterohepatic circulation in a mouse model of liver cancer.
METHODS: A liver cancer model was established in C57BL/6J mice, which were divided into a sham surgery group, a model control group, low-, medium- and high-dose curcumin groups, a STAT3 inhibitor group, a combination intervention group and a cisplatin positive control group. HE staining was used to observe the pathological morphology of liver tissue. Serum biochemical indicators and IL-6 and TGF-β1 levels were measured. STAT3 pathway proteins were detected by Western blot and related gene expression was analyzed by qRT-PCR.
RESULTS: Curcumin dose-dependently inhibited STAT3 signaling activity and reduced the p-STAT3/total STAT3 ratio (P<0.05). In the high-dose curcumin group, serum ALT, AST and TB levels decreased from (254.55±56.14)U/L, (542.01±71.28)U/L and (42.98±8.21)μmol/L to (47.98±10.68)U/L, (135.24±24.12)U/L and (7.91±1.36)μmol/L, respectively (all P<0.05). Curcumin upregulated the expression of BSEP, NTCP and FXR, downregulated Cyp7a1 and upregulated the expression of intestinal Fgf15 and Asbt.
CONCLUSION: Curcumin alleviates liver injury and inflammation while ameliorating bile acid enterohepatic circulation by inhibiting the STAT3 signaling pathway.
OBJECTIVES: To investigate the effects of curcumin on the STAT3 signaling pathway and bile acid enterohepatic circulation in a mouse model of liver cancer.
METHODS: A liver cancer model was established in C57BL/6J mice, which were divided into a sham surgery group, a model control group, low-, medium- and high-dose curcumin groups, a STAT3 inhibitor group, a combination intervention group and a cisplatin positive control group. HE staining was used to observe the pathological morphology of liver tissue. Serum biochemical indicators and IL-6 and TGF-β1 levels were measured. STAT3 pathway proteins were detected by Western blot and related gene expression was analyzed by qRT-PCR.
RESULTS: Curcumin dose-dependently inhibited STAT3 signaling activity and reduced the p-STAT3/total STAT3 ratio (P<0.05). In the high-dose curcumin group, serum ALT, AST and TB levels decreased from (254.55±56.14)U/L, (542.01±71.28)U/L and (42.98±8.21)μmol/L to (47.98±10.68)U/L, (135.24±24.12)U/L and (7.91±1.36)μmol/L, respectively (all P<0.05). Curcumin upregulated the expression of BSEP, NTCP and FXR, downregulated Cyp7a1 and upregulated the expression of intestinal Fgf15 and Asbt.
CONCLUSION: Curcumin alleviates liver injury and inflammation while ameliorating bile acid enterohepatic circulation by inhibiting the STAT3 signaling pathway.
Предметные рубрики MeSH
AnimalsCurcuminSTAT3 Transcription FactorSignal TransductionMiceBile Acids and SaltsMice, Inbred C57BLMaleEnterohepatic CirculationCholesterol 7-alpha-HydroxylaseAntineoplastic AgentsLiverATP Binding Cassette Transporter, Subfamily B, Member 11Organic Anion Transporters, Sodium-DependentInterleukin-6Liver NeoplasmsTransforming Growth Factor beta1Symporters