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The FOXO1/G6PC axis promotes gastric cancer progression and mediates 5-fluorouracil resistance by targeting the PI3K/AKT/mTOR signaling pathway.
Han, Anna; Liu, Taorui; Du, Pan; Wang, Mengying; Liu, Jiajing; Chen, Liyan.
Afiliación
  • Han A; Key Laboratory Pathobiology (Yanbian University), State Ethnic Affairs Commission, Yanji, China.
  • Liu T; Key Laboratory Pathobiology (Yanbian University), State Ethnic Affairs Commission, Yanji, China.
  • Du P; Center for Joint Surgery, Southwest Hospital, Army Medical University, Chongqing, China.
  • Wang M; Key Laboratory Pathobiology (Yanbian University), State Ethnic Affairs Commission, Yanji, China.
  • Liu J; Key Laboratory Pathobiology (Yanbian University), State Ethnic Affairs Commission, Yanji, China.
  • Chen L; Key Laboratory Pathobiology (Yanbian University), State Ethnic Affairs Commission, Yanji, China.
Mol Carcinog ; 63(4): 688-700, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38224261
ABSTRACT
Gastric cancer (GC) is a prevalent malignancy of the digestive system. Distant metastasis and chemotherapy resistance are the crucial obstacles to prognosis in GC. Recent research has discovered that the glucose-6-phosphatase catalytic subunit (G6PC) plays an important role in tumor malignant development. However, little evidence has highlighted its role in GC. Herein, through a comprehensive analysis including profiling of tissue samples and functional validation in vivo and in vitro, we identify G6PC as a crucial factor in GC tumorigenesis. Importantly, we found that the FOXO1/G6PC axis could accelerate GC cell proliferation, metastasis, and 5-Fluorouracil (5-FU) resistance by targeting the PI3K/AKT/mTOR signaling pathway, implicating that as a prospective therapeutic approach in GC.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Gástricas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Gástricas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article