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J Gastroenterol Hepatol ; 39(8): 1684-1694, 2024 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-38747068

RESUMEN

BACKGROUND AND AIM: The impact of cholecystectomy, which blocks the cholecystohepatic shunt pathway (CHSP), on the prognosis of patients with hepatocellular carcinoma (HCC) is unclear. Hepatic secondary bile acids (BAs) inhibit natural killer T (NKT) cell-mediated immunity against HCC, and the regulation of homeostasis of hepatic secondary BAs is controlled by the CHSP. However, the influence of CHSP on NKT cell-mediated immunity against HCC remains unclear. METHODS: The clinical data of hospitalized patients undergoing HCC resection were collected. Meanwhile, an in situ HCC mouse model was established, and the CHSP was augmented using oleanolic acid (OA). RESULTS: After 1:1 propensity score matching, Cox regression analysis revealed that cholecystectomy was an independent risk factor for HCC recurrence after hepatectomy (P = 0.027, hazard ratio: 1.599, 95% confidence interval: 1.055-2.422). Experimentally, when OA enhanced CHSP, a significant decrease was observed in the accumulation of secondary BAs in the livers of mice. Additionally, a significant increase was observed in the levels of C-X-C ligand 16 and interferon γ in the serum and tumor tissues. Further, the percentage of C-X-C receptor 6 (+) NKT cells in the tumor tissues increased significantly, and the growth of liver tumors was inhibited. CONCLUSIONS: This clinical study revealed that cholecystectomy promoted the recurrence after radical hepatectomy in patients with HCC. Preserving the normal-functioning gallbladder as much as possible during surgery may be beneficial to the patient's prognosis. Further investigation into the mechanism revealed that CHSP enhanced NKT cell-mediated immunity against HCC by reducing the hepatic accumulation of secondary BAs.


Asunto(s)
Ácidos y Sales Biliares , Carcinoma Hepatocelular , Neoplasias Hepáticas , Células T Asesinas Naturales , Animales , Carcinoma Hepatocelular/inmunología , Carcinoma Hepatocelular/cirugía , Células T Asesinas Naturales/inmunología , Neoplasias Hepáticas/inmunología , Neoplasias Hepáticas/cirugía , Ácidos y Sales Biliares/metabolismo , Masculino , Humanos , Femenino , Colecistectomía , Modelos Animales de Enfermedad , Ratones , Hepatectomía , Persona de Mediana Edad , Ácido Oleanólico/análogos & derivados , Ácido Oleanólico/farmacología , Hígado/metabolismo , Ratones Endogámicos C57BL , Inmunidad Celular , Recurrencia Local de Neoplasia/prevención & control , Interferón gamma/metabolismo , Factores de Riesgo , Anciano
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