Imaging the impact of Nox4 in cycling hypoxia-mediated U87 glioblastoma invasion and infiltration.

Purpose: We determined the impact of the cycling hypoxia tumor microenvironment on tumor cell invasion and infiltration in U87 human glioblastoma cells and investigated the underlying mechanisms using molecular bio-techniques and imaging.Procedures: The invasive phenotype of U87 cells and xenografts...

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Publicado en:Molecular Imaging & Biology Vol. 14; no. 4; pp. 489 - 500
Autores principales: Hsieh CH, Chang HT, Shen WC, Shyu WC, Liu RS, Hsieh, Chia-Hung, Chang, Hao-Teng, Shen, Wu-Chung, Shyu, Woei-Cherng, Liu, Ren-Shyan
Formato: research Journal Article
Publicado: Springer Nature Aug2012
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Aug2012
      vid: 14
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s11307-011-0516-0
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        atl: Imaging the impact of Nox4 in cycling hypoxia-mediated U87 glioblastoma invasion and infiltration.
      aug:
        au:
          Hsieh CH
          Chang HT
          Shen WC
          Shyu WC
          Liu RS
          Hsieh, Chia-Hung
          Chang, Hao-Teng
          Shen, Wu-Chung
          Shyu, Woei-Cherng
          Liu, Ren-Shyan
        affil: Graduate Institute of Basic Medical Science, China Medical University and Hospital, Taichung, Taiwan
      sug:
        subj:
          Glioma
          Glioma Pathology
          Molecular Imaging Methods
          Oxidoreductases Metabolism
          Animal Studies
          Biochemical Phenomena
          Cell Movement
          Cell Physiology
          Cells
          Genetic Techniques
          Mice
          Neoplasm Invasiveness
          Peptide Hydrolases Metabolism
          Proteins Metabolism
          Reactive Oxygen Species Metabolism
          Transferases Metabolism
      ab: Purpose: We determined the impact of the cycling hypoxia tumor microenvironment on tumor cell invasion and infiltration in U87 human glioblastoma cells and investigated the underlying mechanisms using molecular bio-techniques and imaging.Procedures: The invasive phenotype of U87 cells and xenografts exposed to experimentally imposed cycling hypoxic stress in vitro and in vivo was determined by the matrigel invasion assay in vitro and dual optical reporter gene imaging in vivo. RNAi-knockdown technology was utilized to study the role of the NADPH oxidase subunit 4 (Nox4) on cycling hypoxia-mediated tumor invasion.Results: Cycling hypoxic stress significantly promoted tumor invasion in vitro and in vivo. However, Nox4 knockdown inhibited this effect. Nox4-generated reactive oxygen species (ROS) are required for cycling hypoxia-induced invasive potential in U87 cells through the activation of NF-κB- and ERK-mediated stimulation of MMP-9.Conclusions: Cycling hypoxia-induced ROS via Nox4 should be considered for therapeutic targeting of tumor cell invasion and infiltration in glioblastoma.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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