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Quercetin induced cell apoptosis and altered gene expression in AGS human gastric cancer cells.
Shang, Hung-Sheng; Lu, Hsu-Feng; Lee, Ching-Hsiao; Chiang, Han-Sun; Chu, Yung-Lin; Chen, Ann; Lin, Yuh-Feng; Chung, Jing-Gung.
Afiliación
  • Shang HS; Graduate Institute of Clinical of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
  • Lu HF; Division of Clinical Pathology, Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
  • Lee CH; Department of Clinical Pathology, Cheng-Hsin General Hospital, Taipei, Taiwan.
  • Chiang HS; Department of Restaurant, Hotel and Institutional Management, Fu-Jen Catholic University, New Taipei City, Taiwan.
  • Chu YL; Department of Medical Technology, Jen-Teh Junior College of Medicine, Nursing and Management, Miaoli County, Taiwan.
  • Chen A; Graduate Institute of Basic Medicine, Fu-Jen Catholic University, New Taipei city, Taiwan.
  • Lin YF; International Master's Degree Program in Food Science, International College, National Pingtung University of Science and Technology, Pingtung, Taiwan.
  • Chung JG; Division of Clinical Pathology, Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Environ Toxicol ; 33(11): 1168-1181, 2018 Nov.
Article en En | MEDLINE | ID: mdl-30152185
ABSTRACT
Quercetin is one of the natural components from natural plant and it induces cell apoptosis in many human cancer cell lines. However, no available reports show that quercetin induces apoptosis and altered associated gene expressions in human gastric cancer cells, thus, we investigated the effect of quercetin on the apoptotic cell death and associated gene expression in human gastric cancer AGS cells. Results indicated that quercetin induced cell morphological changes and reduced total viability via apoptotic cell death in AGS cells. Furthermore, results from flow cytometric assay indicated that quercetin increased reactive oxygen species (ROS) production, decreased the levels of mitochondrial membrane potential (ΔΨm ), and increased the apoptotic cell number in AGS cells. Results from western blotting showed that quercetin decreased anti-apoptotic protein of Mcl-1, Bcl-2, and Bcl-x but increased pro-apoptotic protein of Bad, Bax, and Bid. Furthermore, quercetin increased the gene expressions of TNFRSF10D (Tumor necrosis factor receptor superfamily, member 10d, decoy with truncated death domain), TP53INP1 (tumor protein p53 inducible nuclear protein 1), and JUNB (jun B proto-oncogene) but decreased the gene expression of VEGFB (vascular endothelial growth factor B), CDK10 (cyclin-dependent kinase 10), and KDELC2 (KDEL [Lys-Asp-Glu-Leu] containing 2) that are associated with apoptosis pathways. Thus, those findings may offer more information regarding the molecular, gene expression, and signaling pathway for quercetin induced apoptotic cell death in human gastric cancer cells.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Quercetina / Neoplasias Gástricas / Apoptosis Límite: Humans Idioma: En Revista: Environ Toxicol Asunto de la revista: SAUDE AMBIENTAL / TOXICOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Taiwán

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Quercetina / Neoplasias Gástricas / Apoptosis Límite: Humans Idioma: En Revista: Environ Toxicol Asunto de la revista: SAUDE AMBIENTAL / TOXICOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Taiwán